The Beginning Of The Plague?
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The Living Force
There is some info here: _http://journalofcosmology.com/Panspermia5.htmlPerceval said:
"2. TRANSFER OF MICROORGANISMS FROM EARTH TO OUTER SPACE
The Tunguska Space Body (TSB) is the only known body to have had an extremely close interaction with Earth; just about ~5÷10 km above the Earth’s surface, only to escape into space (Napier 2009). We are aware of the impact TSB left on Earth. However we are not aware of the impact the interactions left on the TSB. It would be interesting to investigate if any of Earth’s atmospheric gasses or microorganisms became incorporated into the TSB when it bounced off the upper atmosphere.
It is known that microorganisms exist in significant concentrations in Earths’ atmosphere (Burrows et al., 2009; Griffin 2004; Wainwright et al., 2010). Microorganisms have been found in air samples collected at heights ranging from 41 km (Wainwright et al., 2010) to 77 km (Imshenetsky, 1978). The natural mechanisms which transport microorganisms to the atmosphere are storm activity, volcanic activity, monsoons, and impact events (Joseph and Schild 2010; Wainwright et al., 2010).
In fact, a particular long term study conducted close to the Tunguska Phenomenon site, in the skies of southwestern Siberia, found significant concentrations of culturable microorganisms over an altitude range of 0.5–7 km (Andreeva et al., 2002; Borodulin et al., 2005). This height range is similar to the height range of ~5÷10 km where the TSB interacted with Earth’s atmosphere. Of course, the TSB-Earth interaction was fierce and explosive. However there is a possibility of contamination, either of Earth’s microorganisms into the TSB, or organisms which may have resided in the TSB being deposited on Earth, or both.
3. DISEASES FROM SPACE?
Hoyle, Wickramasinghe, Napier and others (Hoyle and Wickramasinghe 2000, Napier and Wickramasinghe 2010; Wickramasinghe 2010; Wickramasinghe et al., 2009) have provided considerable evidence indicating microbial life can flourish within the heart of comets and may be deposited on other planets including Earth. Wainwright et al., (2010), based on evidence of bacteria in the upper atmosphere and stratosphere, argue that life may be continually incoming from space and outgoing from Earth. Joseph (2009b; Joseph and Schild 2010) has developed a detailed model explaining how microbes can be lofted into the stratosphere and periodically ejected into space during particularly powerful solar storms. Joseph (2009b; Joseph and Schild 2010) has also provided and reviewed evidence that microbes can travel from planet to planet and solar system to solar system encased in asteroids, comets and other stellar debris, and that they can survive the impact and heat of ejection and reentry into the atmosphere. Therefore, there is good reason to suspect that a stellar object striking and skimming along the upper atmosphere could eject microbes into the atmosphere of Earth and become contaminated with microbes already present at these heights.
Joseph (2000, 2009c; Joseph and Schild 2010) has developed a detailed genetic model of cosmic evolution, and has argued that as microbes and viruses are transferred from planet to planet, they exchange and acquire DNA. According to Joseph (2000, 2009c) these genes were then transferred to to the eukaryotic genome, contributing to the evolution of multi-cellular life leading to humans. Likewise, Wainwright et al., (2010) propose that incoming and outgoing microbes may exchange DNA via horizontal gene transfer, and this genetic exchange contributes to the evolution of life on Earth.
Wickramasinghe (2010) also believes that space-traveling microbes and viruses contribute to evolution, but are also responsible for "errors" introduced into the genome. These "errors" result in disease, disability, and death. Hoyle and Wickramasinghe (1979, 1986) have referred to this as "diseases from space."
Is there any evidence that microbes and viruses were deposited on Earth by the TSB or following the Tunguska impact in 1908? The evidence is indirect at best, i.e. the 1918 flu epidemic which killed over 20 million people world wide (Joseph 2009a). It is unknown if the TSB is comet Encke. However, Comet Encke made an extremely close approaches to Earth on June 16, 1908, and again on October 27 1914, and was at perihelion on 1918. And with each approach, Comet Encke shed ice, rock and dust which streaked through the atmosphere of Earth.
According to Hoyle and Wickramasinghe (1979, 1986, 2000; Wickramasinghe 2010; Wickramasinghe et al., 2009) under these circumstances microbes and viruses would be shed from the comet and would be deposited on Earth and could induce disease. Wainwright et al., (2010) argue that microbes from space would exchange DNA with microbes of Earth, and the same has been said of viruses (Joseph and Schild 2010). There is also considerable evidence that the 1918 flu epidemic was due to gene mixing between an already established virus and a completely unknown "new" virus (Joseph 2009a).
As detailed by Joseph (2009a):
"In 2005, scientists from the Armed Forces Institute of Pathology in Washington, D.C., resurrected the 1918 virus from bodies that had been preserved in the permanently frozen soil of Alaska. They soon discovered that a completely new virus had combined with a old virus, exchanging and recombining genes, creating a hybrid that transformed mild strains of the flu virus into forms far more deadly and pathogenic. They also confirmed that the 1918 Spanish flu virus originated in the sky, first infecting birds and then spreading and proliferating in humans."
This paper just came into my attention. I think it is very relevant in the sense that the fragments of hemorrhagic viruses that were speculated to be the cause of the Black Death, are listed as part of our genome, indicating that life on Earth has been exposed to rather dangerous viruses through our evolutionary history which then effected changes in our DNA.
The second paper was linked in the first one and is even more interesting. It expands and backs up Bryant M. Shiller's explanations on "Origin of Life: The 5th Option" (or so it seems to me!). Keeping in mind that "transposable elements" (TE) - which was once considered "junk" DNA - is viral in its origin, it would explain why humanity benefits from periodic plague diseases to give a kick-start or "reformation" to our genetic makeup and accelerate evolution or change through cometary impacts. Both articles are very long, but I bolded in black and red some relevant information. Enjoy!
The second paper was linked in the first one and is even more interesting. It expands and backs up Bryant M. Shiller's explanations on "Origin of Life: The 5th Option" (or so it seems to me!). Keeping in mind that "transposable elements" (TE) - which was once considered "junk" DNA - is viral in its origin, it would explain why humanity benefits from periodic plague diseases to give a kick-start or "reformation" to our genetic makeup and accelerate evolution or change through cometary impacts. Both articles are very long, but I bolded in black and red some relevant information. Enjoy!
Transposable elements and viruses as factors in adaptation and evolution: an expansion and strengthening of the TE-Thrust hypothesis
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3501640/
Abstract
In addition to the strong divergent evolution and significant and episodic evolutionary transitions and speciation we previously attributed to TE-Thrust, we have expanded the hypothesis to more fully account for the contribution of viruses to TE-Thrust and evolution. The concept of symbiosis and holobiontic genomes is acknowledged, with particular emphasis placed on the creativity potential of the union of retroviral genomes with vertebrate genomes. Further expansions of the TE-Thrust hypothesis are proposed regarding a fuller account of horizontal transfer of TEs, the life cycle of TEs, and also, in the case of a mammalian innovation, the contributions of retroviruses to the functions of the placenta. The possibility of drift by TE families within isolated demes or disjunct populations, is acknowledged, and in addition, we suggest the possibility of horizontal transposon transfer into such subpopulations. “Adaptive potential” and “evolutionary potential” are proposed as the extremes of a continuum of “intra-genomic potential” due to TE-Thrust. Specific data is given, indicating “adaptive potential” being realized with regard to insecticide resistance, and other insect adaptations. In this regard, there is agreement between TE-Thrust and the concept of adaptation by a change in allele frequencies. Evidence on the realization of “evolutionary potential” is also presented, which is compatible with the known differential survivals, and radiations of lineages. Collectively, these data further suggest the possibility, or likelihood, of punctuated episodes of speciation events and evolutionary transitions, coinciding with, and heavily underpinned by, intermittent bursts of TE activity.
Introduction
The importance of transposable elements (TEs) to stress responses and adaptation was first proposed by Barbara McClintock who was also the discoverer of TEs (McClintock 1956, 1984). Since then much groundbreaking work has substantiated the view that TEs play a significant role in evolution (Georgiev 1984; Syvanen 1984; Finnegan 1989; Brosius 1991; McDonald 1993; Kidwell and Lisch 1997; Fedoroff 1999; Shapiro 1999; Bennetzen 2000; Bowen and Jordan 2002; Jurka 2004; Kazazian 2004; Biémont and Vieira 2006; Volff 2006; Wessler 2006; Feschotte and Pritham 2007; Muotri et al. 2007; Beauregard et al. 2008; Böhne et al. 2008; Hua-Van et al. 2011; Werren 2011). Building on this body of work, we have proposed TEs as powerful facilitators of evolution (Oliver and Greene 2009a) and have subsequently gone further than others by formalizing this general concept into an explicit, comprehensive, predictive, and testable hypothesis, which we call the “TE-Thrust hypothesis” (Oliver and Greene 2011). The basis of the TE-Thrust hypothesis is that TEs are powerful facilitators of evolution that can act to generate genetic novelties in both an active mode and a passive mode. Active mode: by transposition, including the exaptation of TE sequences as promoters, exons, or genes. Passive mode: when present in large homogeneous populations, TEs can cause ectopic DNA recombination resulting in genomic duplications, deletions or rearrangements (including karyotypic changes). Fecund lineages, those with many species (e.g., rodents and bats, which together make up 60% of mammals), are generally rich in viable (i.e., capable of activity) and active TEs, whereas nonfecund lineages (e.g., monotremes) have mainly nonviable (i.e., incapable of activity) and inactive TEs. Evolutionary transitions, for example, the evolution of the higher primates and evolutionary innovations, such as the mammalian placenta, also appear to be facilitated by TEs (Oliver and Greene 2011). An outline of the TE-Thrust Hypothesis is:
Many eukaryote lineages are able to tolerate some sacrifices in the present, that is, a genomic “load” or population, of mostly controlled, but possibly fitness-reducing TEs. Such lineages may, thereby, fortuitously, gain a continuum of “intra-genomic potential” whose extremities are conveniently described as “adaptive potential” and “evolutionary potential.” This intragenomic potential may be realized in the present, and/or in the descendant lineage(s) of the future. Note that this does not imply any “aim” or “purpose” to evolution, or any ability of evolution to “see” into the future.
As environmental or ecological factors change, or the lineages adopt new habitats, these intragenomic potentials can be realized. For example, adaptive potential can be realized to give small adaptive changes within a lineage, over short periods of time, such as the evolution of insecticide resistance, when insecticides become prevalent in the environment. Evolutionary potential can be realized, over much longer periods of time, perhaps in adaptive radiations, as in some rodents or bats.
At least some unicellular eukaryotic organisms do not appear to tolerate a genomic load of TEs (Galagan and Selker 2004; Pritham 2009), which suggests that TE-Thrust does not operate in all extant biological lineages. However, it is noteworthy that most eukaryotic species known to lack TEs are intracellular parasites with small genomes, including members of the Babesia, Cryptosporidium, and Plasmodium genera (Pritham 2009). This could be due to selection for small cell size and/or because the genomic plasticity engendered by TEs may not provide a net advantage to nonfree-living organisms that exist within a stable environment.
TE-Thrust and Punctuated Equilibrium
Eldredge and Gould (1972) posed the concept of punctuated equilibrium from studies of the fossil record, as opposed to the then prevailing concept of phyletic gradualism. There is now independent support for punctuated equilibrium from studies of extant taxa (Cubo 2003; Pagel et al. 2006; Mattila and Bokma 2008; Laurin et al. 2012), from co-evolution (Toju and Sota 2009), and in extant and ancient genomes of Gossypium species due to intermittent TE activity (Palmer et al. 2012). TE-Thrust provides an intragenomic explanation of punctuated equilibrium (Oliver and Greene 2009a,b, 2011), as has also been suggested by Zeh et al. (2009), via epigenetic changes, and/or endogenization of retroviruses, in response to stress, and Parris (2009), via endogenization of retroviruses and environmental change.
The actual processes of speciation events seem to be poorly understood, but new species are said to emerge from many differing and rare single events (Venditti et al. 2010). However, two almost essential components seem to be necessary: reproductive isolation and intragenomic variation. Of these, intragenomic variation can be readily supplied by the hypothesized TE-Thrust (Oliver and Greene 2011), and reproductive isolation can be provided by a variety of means, including karyotypic changes, polyploidy, hybridization, and physical environmental or ecological factors (Venditti et al. 2010).
Much TE activity (active TE-Thrust) is thought to occur in intermittent bursts that interrupt more quiescent periods of low activity (Bénit et al. 1999; Marques et al. 2005; Cantrell et al. 2005; Pritham and Feschotte 2007; de Boer et al. 2007; Ray et al. 2008; Zeh et al. 2009; Erickson et al. 2011). These punctuation events can occur especially after intermittent infiltrations or amplifications of TEs. New acquisitions of TEs can be due to:
Intermittent horizontal transposon transfer (HTT) (Schaack et al. 2010). This appears to be relatively rare, and probably tends to occur more often with some DNA-TEs, LTR retro-TEs, and the Bov-B LINE.
The de novo synthesis of chimeric elements, for example, the hominid specific SVA (Wang et al. 2005). This is probably rare.
The de novo syntheses of various SINEs, the younger ones (<100 Myr) of which are lineage specific (Piskurek et al. 2003; Kramerov and Vassetzky 2011). This is probably rare.
Intermittent endogenizations of various RNA viruses (Bénit et al. 1999; Belyi et al. 2010; Horie et al. 2010). This may be relatively common, especially in mammals.
Hybridization, especially in angiosperms (Michalak 2010). This appears to be common.
Intermittent de novo modifications to successive families of TEs (e.g. L1 LINEs). This is relatively common.
An example of an intermittent burst is the L1 LINE in ancestral primates, where among a large number of overlapping families, L1PA6, L1PA7, and L1PA8 were apparently amplified intensively around 47 Mya. This seemingly contributed to a very large Alu SINE, and retrocopy, amplification at this time (Ohshima et al. 2003). TEs can result in the acceleration of the evolution of genes in a myriad of ways (Böhne et al. 2008; Goodier and Kazazian 2008; Hua-Van et al. 2011), providing a means for rapid species divergences in the affected lineages.
Modes of TE-Thrust
All the hypothesized modes of TE-Thrust shown below are consistent with the data tabulated in Oliver and Greene (2011), but are expressed herein in different ways. All of them refer only to the potential for adaptation or evolution due to the hypothesized TE-Thrust. As other facilitators of evolution will possibly also be active in addition to TE-Thrust, and as environmental and ecological factors can frequently change, all these hypothesized capabilities of TE-Thrust need to be predicated by “if all else is equal”. These modes of TE-Thrust are extremes of continuums, so intermediate modes must occur.
Mode 1. Evolutionary potential may be realized, in concert with, or following, significant intermittent bursts of TE activity, in viable and heterogeneous TE populations, whether large or small. This can underlie what we designate as “Type I” punctuated equilibrium (stasis with punctuation events), due to intermittent active TE-Thrust.
Mode 2. Evolutionary potential may be realized, in concert with, or following, significant bursts of TE activity, in large viable and homogenous TE populations. This can result in what we designate as “Type II” punctuated equilibrium (gradualism with punctuation events) due to both ongoing TE-Thrust (largely passive), and to intermittent active TE-Thrust. If the TE population is small, then only intermittent active TE-Thrust is likely to occur as per mode 1.
Mode 3. Nonviable heterogeneous TE populations, whether large or small, may result in evolutionary stasis, due to a lack of both active and passive TE-Thrust.
Mode 4. If a nonviable TE population is both large and homogeneous, and not too degraded by mutations, then gradualism type evolution may occur, due largely to passive TE-Thrust. If the TE population is small, then little TE-Thrust is likely to occur as per mode 3.
An Expansion of the TE-Thrust Hypothesis
Herein, the TE-Thrust hypothesis is further expanded from its original formulation. We acknowledge that in addition to TE-Thrust, other nongenomic facilitators of evolution may play a part in radiations and evolution, such as dynamic external factors, including geological, environmental, and ecological changes. Such factors may result in fragmentation of populations into small local demes, or larger disjunct sub-populations, which can result in reproductive isolation with possible divergence into novel taxa (Wright 1931; Eldredge 1995; Jurka et al. 2011). In addition to alleles drifting to fixation or extinction in demes, TE families likely also do so (Jurka et al. 2011) and we are in agreement with this. Additionally, in TE-Thrust we hypothesize that novel TEs as described above, may very occasionally be introduced into, or arise within, some demes or disjunct populations, but not into others, ultimately causing evolutionary transitions or the evolution of new taxa. We view the carrier subpopulation (CASP) hypothesis (Jurka et al. 2011) to be complementary to TE-Thrust, as it is about the fixation of TEs in populations and the details of mechanisms, or origins, of speciation, which were previously not included in the TE-Thrust hypothesis. The CASP hypothesis gains some support from the cotton genus (Gossypium) specific Gorge retro-TEs (Palmer et al. 2012), as Gorge seems to have spread to fixation in a small progenitor population of Gossypium. Indeed, both hypotheses are in agreement in strongly relating TEs to speciation and evolution. However, we suggest that karyotypic changes due to TE presence and activity, are among the factors that produce the reproductive isolation necessary for speciation, although we agree that geographic isolation into demes, niche availability, and many other phenomena (e.g., pheromone changes in insects) are also important factors.
We note that adaptive evolution via natural selection is, but one of the forces of evolutionary change. Other important forces, all of which are nonadaptive, comprise mutation, recombination, and random genetic drift (Lynch 2007). As TE-Thrust emphasizes a key intragenomic role for TEs in mutation and recombination, it fits comfortably with a growing body of evidence indicating that a significant portion of evolutionary changes are not adaptive in nature, but result from the accumulation of mildly deleterious mutations that can become fixed by genetic drift in populations of relatively small size (Fernández and Lynch 2011). Indeed, although the occasional highly deleterious TE insertion will be rapidly culled by purifying selection, TE insertions can themselves be viewed overall as an accumulation of neutral to mildly deleterious mutations that are subject to genetic drift. Activation of TEs, for example, during stress, or horizontal transfer of TEs etc., provides powerful complements to genetic drift. Thus, TEs accumulate by nonadaptive processes and can underpin nonadaptive change, and they also readily provide the raw material for future beneficial traits capable of undergoing positive selection.
We recognize that there are many known genomic facilitators of evolution, besides TE-Thrust. A few apposite examples are: symbiosis (Ryan 2007, 2009); hybridization (Ryan 2006; Larsen et al. 2010); noncoding RNA (Heimberg et al. 2008; Mattick 2011); horizontal gene transfer (Richards et al. 2006); whole genome duplications (Hoffmann et al. 2012), and viral driven evolution (Villarreal 2005, 2009; Ryan 2007; Villarreal and Witzany 2010; Feschotte and Gilbert 2012). Some facilitators of evolution may have greater importance in some clades than in others. For example, whole genome duplication (polyploidy) is apparently quite important in the evolution of angiosperms (Soltis et al. 2004). Ryan (2006) includes several of the examples above under the general descriptor “genomic creativity”.
Horizontal Transfer of TEs in TE-Thrust
Mobile DNA has been classified into Class I retro-TEs (e.g., LTR elements, LINEs, and SINEs), and Class II DNA-TEs, composed of subclasses 1 (e.g., Tc1-Mariner and hAT) and 2 (Helitron and Maverick), as have been described and reviewed elsewhere (Wicker et al. 2007; Böhne et al. 2008; Goodier and Kazazian 2008; Kapitonov and Jurka 2008; Hua-Van et al. 2011). The horizontal transfer of TEs (horizontal transposon transfer or HTT) has previously been proposed as a major force driving genomic variation and biological innovation (Schaack et al. 2010). DNA-TEs have long been known to be capable of HTT, for example, the P-element DNA-TE in Drosophila (Anxolabéhère et al. 1988; Daniels et al. 1990); the Mariner DNA-TE in various insects (Maruyama and Hartl 1991; Robertson and Lampe 1995; Lampe et al. 2003), and DNA-TEs in the bat Myotis lucifugus (Pritham and Feschotte 2007; Ray et al. 2007). However, HTT of retro-TEs, has been less well documented, except for some examples, including the patchily distributed Bov-B LINE, (Kordiš and Gubenšek 1998; Gogolevsky et al. 2008) and the Gypsy-like retro-TEs (Herédia et al. 2004).
Although probably infrequent, HTT is an important aspect of the TE-Thrust hypothesis that has so far only been given cursory attention (Oliver and Greene 2009a, 2011). Over 200 cases of HTT have been documented (Schaack et al. 2010), 12 of which were between different phyla. About a half of these known HTTs involved retro-TEs, most of which were LTR retro-TEs. The remaining HTTs involved a variety of DNA-TEs. Horizontal transfer is an important part of the life cycle of TEs, as they generally accumulate mutations and eventually become nonviable in the genomes they occupy. This can downgrade the efficacy of TE-Thrust. However, they are sometimes enabled, via chance events, to periodically make fresh starts with fully functional elements, in the genomes of other lineages. At least some TEs appear to be able to endure in the absence of HTT. For example, the LINE 1 (L1) retro-TE in mammals has persisted for 100 Myr with no known evidence of HTT (Furano et al. 2004; Khan et al. 2006), although it has now become nonviable in a few mammalian lineages (Casavant et al. 2000; Boissinot et al. 2004; Cantrell et al. 2008; Platt and Ray 2012).
Viruses and bacteria appear to be likely vectors of HTT (Piskurek and Okada 2007; Schaack et al. 2010; Dupuy et al. 2011), but endoparasites and intracellular parasites are among other possible vectors that have been proposed (Silva et al. 2004; Schaack et al. 2010). Empirical data (Anxolabéhère et al. 1988; Cantrell et al. 2005; de Boer et al. 2007; Pritham and Feschotte 2007; Ray et al. 2008) and simulations (Le Rouzic and Capy 2005) both suggest that TE amplification occurs immediately after HTT of a viable TE copy.
Holobionts and Holobiontic Genomes, and The Importance of the Highly Mobile Retroviruses
Exogenous retroviruses can become endogenized, and can be united with the host genome into a holobiontic genome in a new holobiont (Box 1). Holobiont is a symbiological term that means the partnership, or union, of symbionts (Rosenberg et al. 2007; Ryan 2007; Gilbert et al. 2010). For example, the ERVWE1 locus in the human genome comprises a conserved envelope (env) gene together with the conserved 5′ LTR of a retrovirus that contains regulatory elements. This locus, additionally, includes sections of human genetic sequences and these also play a role in regulation of the env gene, which codes for Syncytin-1 (Mi et al. 2000). Syncytin-1 has a crucial function in trophoblast cell fusion in ape placental morphogenesis (Mi et al. 2000), which strongly suggests that selection has occurred at the level of the holobiontic genome in the human plus retrovirus holobiont (Ryan 2006).
Retroviruses appear to be the most mobile of all “mobile DNA” as they can exist exogenously as infectious, or persisting viruses, as well as by becoming endogenized in host germ lines (Hughes and Coffin 2001, 2004; Ryan 2006). Exogenous retroviruses are distinct entities to those species whose genomes into which they endogenize to become an ERV, and they have an extracellular or virion stage, with a protein capsid. ERVs then are a part of a holobiont organism. Other TEs in a genome are not considered to be a part of a holobiont, as they seemingly can only transfer from genome to genome, and can have no independent existence like that of an exogenous retrovirus species.
Endogenized retroviruses (ERVs) can multiply within a genome either by repeated endogenizations, or by retrotransposition within the genome (Belshaw et al. 2004; Wang et al. 2010). Over time, due to recombinations between their LTRs, and deletions, ERVs often exist mostly as solo LTRs or sLTRs, (Sverdlov 1998). Many Class I elements are related to retroviruses, namely the Copia, Gypsy, and BEL/Pao subclasses of LTR retro-TEs, which have LTRs (long- terminal repeats), but lack an env gene.
Retroviruses are present among all placental mammals (Bénit et al. 1999), are largely restricted to vertebrates, and are particularly abundant in mammals (Villarreal 2005). Retroviruses have been endogenized in mammalian germ lines many times during the evolution of mammals. These ERVs have been a very important factor in their evolution (Villarreal 2005), and are particularly associated with that mammalian innovation, the placenta (Oliver and Greene 2011). Endogenized retroviruses, and the role they play in evolution, have been extensively detailed elsewhere (Villarreal 1997, 2004, 2005, 2009; Ryan 2003, 2006, 2007; Feschotte and Gilbert 2012).
Endogenous nonretroviral RNA virus elements, notably Bornaviruses, have also been found in mammalian genomes, including several primates and several rodents, and these viral sequences appear to have function (Belyi et al. 2010; Horie et al. 2010). Indeed, all major types of eukaryotic viruses can give rise to endogenous viral elements or EVEs (Feschotte and Gilbert 2012). Thus, viral-eukaryote holobiont organisms appear to be not uncommon, and these could have lead to significant evolutionary innovation. This enhances the explanatory power of the TE-Thrust hypothesis.
Retroviruses and the Evolution of the Mammalian Placenta
The placenta represents a major evolutionary innovation that occurred over 160 Mya at the time of the divergence of the placental mammals. The circulatory and the metabolic benefits provided by this transient organ to the growing embryo and fetus have been well investigated, but less so well understood is the origin of the placenta. The invasive syncytial plate, the precursor to the placenta, and the rapidly growing trophoblast, are developmentally unique to mammals (Harris 1991). Harris proposes that prior to the divergence of placental mammals, developing embryos became infected at an early intrauterine stage with retroviruses, which gave rise to cellular proliferation and creation of the trophoblast. This may then have resulted in the formation of the highly invasive “tumor-like” vacuolated and microvillated syncytial plate and a primitive placenta (Harris 1991). Although to date, there is no proof that the fusogenic ERVs of premammals resulted in the evolution of the mammalian placenta (Harris 1991; Dupressoir et al. 2009) it seems likely to be correct. Supporting evidence comes from the egg-laying platypus, which has a genome that is devoid of ERVs, although there are some thousands of ancient Gypsy-class LTR retro-TEs (Warren et al. 2008). In contrast, all examined placental mammal genomes do contain many ERVs (Mayer and Meese 2005; Villarreal 2005), with ERV/sLTRs constituting approximately 8% and 10% of the human and mouse genomes, respectively (Waterston et al. 2002). Atypically, the placenta exhibits global DNA hypomethylation, which allows many ERVs and retro-TEs to retain transcriptional activity in this tissue (Rawn and Cross 2008). Such a permissive environment for expression of TEs facilitates their exaptation as coding or regulatory sequences, and indeed, the LTRs of ERVs contain promoter activity that can confer tissue-specific expression in the placenta, as for example, the CYP19A1, IL2RB, NOS3, and PTN genes, which are solely expressed by an LTR promoter (Cohen et al. 2009). Although there are few known unique placenta-specific genes, numerous genes expressed in the human placenta are derived from retro-TEs and ERVs (Rawn and Cross 2008). Most notable are the fusogenic, ERV env-derived, syncytin-1, and syncytin-2 (Mi et al. 2000; Blaise et al. 2003), with syncytin-2 also having an immunosuppressive function (Kämmerer et al. 2011). The efficient adaptive immune systems of mammals must fail to initiate an immune reaction to the antigens of their embryos and placentas, and mammals alone are very highly infected with the generally immunosuppressive endogenous retroviruses (Villarreal 1997). Intriguingly, retroviruses are abundant around sperm heads and also coat the female placenta (Steele 2009). The advantages of the placenta could possibly explain why extant placental mammals number well over 5,000 species, whereas there are less than 300 extant species of marsupials (Pough et al. 2009).
Evolvability and the TE-Thrust Hypothesis
Mutation, including gene duplication and other DNA changes, is the driving force of evolution at both the genic and the phenotypic levels (Nei 2005, 2007). Significantly, Shapiro (2010) proposes that it is mobile DNA movement, rather than replication error that is the primary engine of protein evolution. Along the same lines, Hua-Van et al. (2011) stress TEs as a major factor in evolution, whereas Muotri et al. (2007) proposes that “handy junk” can evolve into “necessary junk”. Wagner (Heard et al. 2010), in support of our original concepts (Oliver and Greene 2009a) states that, in general, “the kinds of genetic changes that are possible depend on what kinds of TEs are present and active at any particular time”, in the evolution of each lineage. Thus, the potential for evolutionary innovations differs over time, contradicting the concept of gradualism in lineages. Caporale (2009) posits that “selection must act on the mechanisms that generate variation, much as it does on beaks and bones”. Earl and Deem (2004), with no mention of TEs, propose the evolution of mechanisms to facilitate evolution, and describe evolvability as a selectable trait. Further to this, Woods et al. (2011) found experimental evidence, in a study of bacteria that long-term evolvability may be important for determining the ultimate success of a lineage, and that less fit lineages with greater evolvability may eventually out-compete lineages with greater fitness. All these lines of reasoning, and associated experimental data, are in good accord with the TE-Thrust hypothesis.
Reduced “Fitness” versus enhanced “Adaptive Potential” and “Lineage Selection”
Accumulation of TEs in the genome of Drosophila melanogaster has been found to be associated with a decrease in fitness (Pasyukova et al. 2004). The reduced “fitness” in Drosophila may be an extreme case, because in D. melanogaster TEs cause over 50% of de novo mutations (Pasyukova et al. 2004). In contrast to D. melanogaster, de novo disease-causing insertions in humans are relatively rare (Deininger and Batzer 1999; Kazazian 1999; Chen et al. 2005; Hedges and Batzer 2005), whereas TE activity in the laboratory mouse falls between these two extremes (Kazazian 1998; Waterston et al. 2002; Maksakova et al. 2006). There is, however, no conflict with the TE-Thrust hypothesis with this finding in Drosophila, as despite a fitness loss in some individuals in the present, there can be a fortuitous gain in adaptive potential to the lineage as a whole. TEd-alleles (TE- deactivated or destroyed alleles), for example, usually lower the fitness of the lineage. However, TEm-alleles (TE-modified alleles, which can be modified in either regulation or function, or duplicated), for example, increase the genetic diversity, and hence the adaptive potential, of the lineage. These TEm-alleles allow the lineage to adapt to environmental/ecological challenges in the present. Also, importantly, this adaptive potential may be latent in the present, and only be realized in the future, as environmental/ecological challenges change. This latent adaptive potential then, increases the chances of the long-term survival of the lineage. In other words, TE-Thrust can result in latent adaptive potential (also called standing variation), which can be realized, if needed, in the future, and can result in the differential survival of lineages. This is the rationale for positing lineage selection in the TE-Thrust hypothesis (Oliver and Greene 2009a,b, 2011).
Realizable “Adaptive Potential” Due to TE-Thrust
TE-Thrust is proposed to have facilitated adaptive change, as we highlighted in the simian lineage (Oliver and Greene 2011). The ongoing ability of TEs to provide realizable adaptive potential is illustrated by TE-generated polymorphic traits identified in isolated populations of laboratory-bred mice (Table 1), as well as by structural variation in the human genome still being created by L1 activity (Ewing and Kazazian 2010).
[...]A specific example of an adaptive benefit from TE activity is the development of insecticide resistance in the Hikone-R strain of Drosophila melanogaster. [...] These four steps have occurred within 70 years in the Hikone-R strain of Drosophila melanogaster, and the more derived the allele, the greater the resistance (Schmidt et al. 2010). Such allelic successions, whereby different adaptive alleles are substituted sequentially have been demonstrated in several other studies of insecticide resistance (Schmidt et al. 2010).[...]
The Failure of Mutation Breeding
In a review, Lönnig (2005), described how, despite early enthusiasm and sustained effort, mutation breeding (in either plants or animals) has never been successful. The mutations caused by mutagens usually produced weaker or nonfunctional alleles of wild type genes. In TE-Thrust, however, the TEs usually consist of functional coding or exaptable sequences, and often also of potent regulatory sequences, so that by insertion and in many other ways, for example, exon shuffling in the active mode and ectopic recombination in the passive mode, they can make many beneficial changes, although they may sometimes do damage (Oliver and Greene 2009a,b, 2011). TEs can alter the regulation or the structure of alleles, or duplicate them (Darboux et al. 2007; González et al. 2009, 2010; Schmidt et al. 2010) creating TEm-alleles. Therefore, although attempted breeding, adaptation or evolution, using mutagens to generate alternative alleles almost always does not work (Lönnig 2005), adaptation or evolution using TE-Thrust generating TEm-alleles relatively often does work. This is not to say that other types of mutation, such as point changes, are not important in evolution. In fact, in addition to their general importance in evolution, such mutations often complement TE-Thrust, for example, by modifying TE-duplicated sequences.
Reduced “Fitness” versus Enhanced “Evolutionary Potential”
The question of whether or not the possible lowering of fitness in a lineage by TEs can result in enhanced evolutionary potential may be simplified into two competing hypotheses:
The Null Hypothesis: TE-Thrust is not causal to adaptation, speciation, punctuation events, or evolution.
The Alternative Hypothesis: TE-Thrust is causal to adaptation, speciation, punctuation events, and evolution.
Testing the Hypotheses
Recent/ancient speciation and the alternative (TE-Thrust) hypothesis
In the absence of events, such as intermittent de novo modifications to successive families of TEs, de novo SINE synthesis, HTT, or de novo synthesis of chimaeric TE elements, TE bursts in lineages eventually tend to fade to inactivity, with TEs becoming nonviable and degraded by the accumulation of deleterious mutations. An example is the apparent loss of L1 element activity in a number of species. These include the spider monkey, thirteen-lined ground squirrel, megabats, and sigmodontinae rodents (Casavant et al. 2000; Boissinot et al. 2004; Cantrell et al. 2008; Platt and Ray 2012), although at least in the case of the sigmodontinae, which have undergone rapid fecund speciation with numerous karyotypic changes, the loss of viable LINEs appears to have been more than compensated for by massive endogenisations of ERVs (Cantrell et al. 2005; Erickson et al. 2011). As TE-Thrust predicts that lineages lose their adaptability as overall TE activity and integrity fades, the loss of TE viability over time provides an intragenomic explanation to help account for the high rate of background extinction that has been a prevalent feature of life on earth (Raup 1994). In contrast, lineages harboring young TE families are associated with recent speciation. This is well exemplified in the mammals where species with the highest numbers of young TE families, such as the mouse, rat, bat, rhesus macaque, and human, represent the largest extant mammalian orders of rodents, bats, and primates (Jurka et al. 2011). Very species-poor extant mammalian lineages, such as the alpaca, elephant, tenrec, armadillo, and platypus, do not harbor any young families of TEs (Jurka et al. 2011). Nevertheless, TE-Thrust predicts more ancient speciation events being attributed to older families of TEs, when they were young, and this is supported by phylogenetic analyses (Jurka et al. 2011). These data are consistent with the Alternative (TE-Thrust) Hypothesis.
The vesper bats and the alternative (TE-Thrust) hypothesis
The radiation of the vesper bats (family Verspertilionidae) appears to support the Alternative Hypothesis and the active mode of TE-Thrust. The vesper bats, which have an almost worldwide distribution (Nowak 1994), are a fecund lineage (407 species of the approximately 930 species of microbats or 8–9% of all extant mammal species), and include Myotis, the most speciose mammalian genus with about 103 members. Significantly, vesper bats are somewhat unique in having many viable and active DNA-TEs that have been nonviable in most other mammals for 37 Myr (Pace and Feschotte 2007).
The early radiation of the vesper bats is proposed to have been due to HTT of Helitron DNA-TEs, called Helibat, into the vesper bat lineage about 30–36 Mya (Pritham and Feschotte 2007).
Amplification of DNA-TEs is thought to follow HTT in a naive lineage, which can result in innovations in the genome (Pace et al. 2008).
Helibat has amplified explosively up to at least 3.4% of the Myotis lucifugus genome (Ray et al. 2008).
HTT of Helitrons, especially, can lead to diversification, and to dramatic shifts in the trajectory of genome evolution (Thomas et al. 2010).
HTT of of DNA-TEs can also lead to horizontal gene transfer (Thomas et al. 2010).
Although Helitrons have not been detected in other mammals besides the vesper bats, they are abundant in plants, invertebrates, and zebrafish, and have been implicated in large-scale gene duplication and exon shuffling.
There were other multiple waves of HTT of DNA-TEs in the bat lineage coinciding with a period of their rapid diversification 16–25 Mya (Teeling et al. 2005; Pritham and Feschotte 2007; Ray et al. 2008).
A further burst of New World Myotis diversification 12–13 Mya was noted (Stadelmann et al. 2007), corresponding well with the period that the most active transposition of a variety of DNA-TEs is estimated to have occurred (Ray et al. 2008).
Such repeated waves of TE activity suggest a mechanism for generating the genetic diversity needed to result in the evolution of such great species richness as is observed in the vesper bats (Ray et al. 2008).
Active retro-TEs, namely L1 LINEs (Cantrell et al. 2008) and VES SINEs (Borodulina and Kramerov 1999), have also been found in vesper bats.
This mix of viable DNA-TEs and retro-TEs, unknown in other mammals, could have resulted in large architectural and organizational changes in their genomes and aided in the Myotis diversification, enabling adaptation to very diverse ecological niches within this lineage (Pritham and Feschotte 2007; Thomas et al. 2011). This suggests that much active TE-Thrust has operated during the very large radiation of the vesper bats during the last 36 Myr. A lack of data presently obscures any conclusions regarding any possible involvement of passive TE-Thrust. The predicted evolutionary outcome of such intermittently active populations of TEs is either gradualism or stasis with punctuation events, (Type I or II punctuated equilibrium). Current data suggest that this is correct for the Verspertilionidae.
The Muridae Rodents and the Alternative (TE-Thrust) Hypothesis
The extensive radiation of the Old World Muridae (the Murinae) appears to support the Alternative Hypothesis, and both the active and the passive modes of TE-Thrust. The rodents are the most fecund mammalian order comprising about 40% of mammals with an almost worldwide distribution. The Muridae family, which include the true mice and rats, have been particularly successful and account for about two-thirds of all rodent species. Representatives of the subfamily Murinae (Mus and Rattus) possess large populations of relatively homogenous retro-TEs, many of which are viable and active (Table 2).
Table 2
Table 2
Presence and Viability of Transposable Elements (TEs) in Distinct Mammalian Species
The Old World mouse (Mus) and rat (Rattus), with some 50–60 species each in their respective genera, have genomes comprised of about 40% largely homogenous genomic TEs. These include numerous viable and mostly highly active L1 LINEs and few nonviable ancient L2 LINEs, giving a LINE total of 22%. SINEs comprise a further 7% and most (92%) are lineage specific, viable, and effective, although slightly diverse, with only few being the nonviable ancient MIR SINEs. Less than 1% of their genomes are composed of nonviable DNA-TEs (Waterston et al. 2002; Gibbs et al. 2004). The mouse has about 10% ERV/sLTRs, many of which are very active and are closely related to mouse exogenous retroviruses (Maksakova et al. 2006).
The fitness cost of their greatly enhanced evolutionary potential is higher than in humans, as previously noted (Maksakova et al. 2006).
Although the generally small size of many rodents probably aided in their diversification, there has seemingly been much active TE-Thrust, as indicated by the growing number of documented examples of rodent-specific traits generated by TEs (Table 3). They are also quite well suited to passive TE-Thrust, as they have large homogenous populations of TEs to facilitate TE-mediated duplications, inversions, deletions or karyotypic changes. The predicted evolutionary outcome of large homogenous and intermittently active populations of TEs is gradualism with punctuation events (Type II punctuated equilibrium), as in the hypothesized mode 2 of TE-Thrust.
Table 3
Table 3
Specific Examples of Transposable Elements (TEs) Implicated in Rodent-Specific Traits
The naked mole rat and the alternative (TE-Thrust) hypothesis
In sharp contrast to Mus and Rattus, which are both very rich in species and have abundant viable and active TEs (Waterston et al. 2002; Gibbs et al. 2004), the rodent genus Heterocephalus, also in the family Muridae, has only one species (Wilson and Reader 2005). In support of the Alternative Hypothesis, sequencing of H. glaber (Kim et al. 2011), the very atypical, physiologically unique, eusocial, and long-lived naked mole rat, has shown that it possesses a nonviable and relatively small mobilome consortium (Table 2).
The TEs of the naked mole rat, although they are homogenous and constitute 25% of the genome, are highly divergent, indicating they have been both nonviable and inactive for a very long time (Kim et al. 2011).
As most mammals have 35–50% TEs, this suggests that a substantial portion of its TEs may have been lost altogether.
The data indicate that H. glaber has had little or no TE-Thrust, except in the remote past, and if all else is equal, it is in stasis or gradualism. (Note: As viable and active TEs are known to occasionally cause harmful mutations, these data additionally suggest that there possibly could be less genetic disease and cancer in the individuals of species, such as H. glaber).[...]
Summary of the evidence for the alternative (TE-Thrust) hypothesis
It can, of course, be argued that this evidence in mammals (microbats, rodents, and the platypus), reptiles (the green anole lizard and the tuatara), and the evolution of the mammalian placenta, is all only circumstantial evidence, and therefore does not demonstrate a causal link between TE-Thrust and enhanced evolutionary potential. This argument is weakened by the abundance of young families of TEs in the largest extant mammalian orders of rodents, bats, and primates, and their absence in the elephant, alpaca, tenrec, armadilo, and platypus. The argument of “only circumstantial evidence” is further weakened by the wide range of known conserved and/or beneficial genomic modifications that are due to TEs in various lineages (Brosius 1999; Miller et al. 1999; Kidwell and Lisch 2001; Nekrutenko and Li 2001; van de Lagemaat et al. 2003; Jordan et al. 2003; Kazazian 2004; Shapiro and Sternberg 2005; Volff 2006; Böhne et al. 2008; Oliver and Greene 2009a, 2011). Therefore, it seems that a causal link between recent TE activity, sometimes resulting in reproductive isolation, and recent speciation events is indeed likely.
Some hard evidence can be provided with regard to adaptive potential and adaptive evolution in insecticide resistance by insects in the last 70 years, and adaptation to temperate climates in the last few centuries. However, a punctuation event is estimated to take between 15,000 and 40,000 years (Gould 2002). It appears then that, as yet, bursts of TE activity and punctuation events cannot be dated accurately enough to establish any definite relationship. However, some apparent correlations have been reported, suggesting that increased TE activity may indeed be basal to, or coincident with, punctuation events and evolutionary transitions, speciation, or large radiations. Some examples of these, in addition to those detailed above, are:
Ohshima et al. (2003) found bursts of Alu SINE and retrocopies coincident with the radiation of the higher primates 40–50 Mya.
DNA-TE activity coincided with speciation events in salmonoid fishes (de Boer et al. 2007).
Bursts of transposition of BS element transposition have also shaped the genomes of at least two species of Drosophila, D. mojavensis and D. recta (Granzotto et al. 2011).
There are numerous examples of bursts of TE activity that often follow polyploidization events (Comai 2000), or hybidization (Michalak 2010), in angiosperms, leading to speciation.
Some suggest that a role for TEs in speciation is speculative (Hua-Van et al. 2011), whereas others have given data, which they readily acknowledge specifically suggests TE involvement in taxon radiations (de Boer et al. 2007; Pritham and Feschotte 2007; Ray et al. 2008; Thomas et al. 2011). In our interpretation of the available data, we suggest that, if all else is equal, minimal or passive TE-Thrust is likely to result in stasis or gradualism, whereas active TE-Thrust is likely to be causal to innovative evolution (e.g., the placenta), punctuation events and radiations, as in our hypothesized four modes of TE-Thrust (Oliver and Greene 2011). However, we readily acknowledge that some punctuation events may be caused by other facilitators of evolution.
Conclusions
The field of evolutionary biology has seemingly paid more attention to the outcomes of genetic mutation in terms of the generation of variants and their selection within populations than the mechanisms by which mutations emerge in the first place. Although small-scale DNA base changes and deletions are important in evolution, TEs (and viruses) are uniquely placed, via TE-Thrust, to expeditiously cause complex and/or large-scale changes and thereby help explain macroevolutionary change and the emergence of highly innovative adaptations. Much still remains to be investigated, such as the relevance of TE-Thrust to other classes and phyla. Only a small number of lineages in the metazoans: the mammals and to a lesser extent, a very few lineages of the insects, plants, and reptiles, have been considered with regard to the TE-Thrust hypothesis to date. As increasing numbers of genomes are being sequenced, it would be interesting to investigate the link between TEs, exogenous viruses, and enhanced adaptive potential, enhanced evolutionary potential, evolutionary transitions, and the occurrence of punctuation events, in the lineages of other taxa. It seems likely that in the great diversity of extant lineages, TE-Thrust and other facilitators of evolution will have had a greater or lesser impact on adaptation and evolution. There seems to be little doubt, however, that TEs and viruses have played a major and prominent role in the evolution of almost all life on earth, and that TEs and viruses need to be recognized and included, as the TE-Thrust hypothesis, in a much needed extension and modification in evolutionary theory.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3501640/
Abstract
In addition to the strong divergent evolution and significant and episodic evolutionary transitions and speciation we previously attributed to TE-Thrust, we have expanded the hypothesis to more fully account for the contribution of viruses to TE-Thrust and evolution. The concept of symbiosis and holobiontic genomes is acknowledged, with particular emphasis placed on the creativity potential of the union of retroviral genomes with vertebrate genomes. Further expansions of the TE-Thrust hypothesis are proposed regarding a fuller account of horizontal transfer of TEs, the life cycle of TEs, and also, in the case of a mammalian innovation, the contributions of retroviruses to the functions of the placenta. The possibility of drift by TE families within isolated demes or disjunct populations, is acknowledged, and in addition, we suggest the possibility of horizontal transposon transfer into such subpopulations. “Adaptive potential” and “evolutionary potential” are proposed as the extremes of a continuum of “intra-genomic potential” due to TE-Thrust. Specific data is given, indicating “adaptive potential” being realized with regard to insecticide resistance, and other insect adaptations. In this regard, there is agreement between TE-Thrust and the concept of adaptation by a change in allele frequencies. Evidence on the realization of “evolutionary potential” is also presented, which is compatible with the known differential survivals, and radiations of lineages. Collectively, these data further suggest the possibility, or likelihood, of punctuated episodes of speciation events and evolutionary transitions, coinciding with, and heavily underpinned by, intermittent bursts of TE activity.
Introduction
The importance of transposable elements (TEs) to stress responses and adaptation was first proposed by Barbara McClintock who was also the discoverer of TEs (McClintock 1956, 1984). Since then much groundbreaking work has substantiated the view that TEs play a significant role in evolution (Georgiev 1984; Syvanen 1984; Finnegan 1989; Brosius 1991; McDonald 1993; Kidwell and Lisch 1997; Fedoroff 1999; Shapiro 1999; Bennetzen 2000; Bowen and Jordan 2002; Jurka 2004; Kazazian 2004; Biémont and Vieira 2006; Volff 2006; Wessler 2006; Feschotte and Pritham 2007; Muotri et al. 2007; Beauregard et al. 2008; Böhne et al. 2008; Hua-Van et al. 2011; Werren 2011). Building on this body of work, we have proposed TEs as powerful facilitators of evolution (Oliver and Greene 2009a) and have subsequently gone further than others by formalizing this general concept into an explicit, comprehensive, predictive, and testable hypothesis, which we call the “TE-Thrust hypothesis” (Oliver and Greene 2011). The basis of the TE-Thrust hypothesis is that TEs are powerful facilitators of evolution that can act to generate genetic novelties in both an active mode and a passive mode. Active mode: by transposition, including the exaptation of TE sequences as promoters, exons, or genes. Passive mode: when present in large homogeneous populations, TEs can cause ectopic DNA recombination resulting in genomic duplications, deletions or rearrangements (including karyotypic changes). Fecund lineages, those with many species (e.g., rodents and bats, which together make up 60% of mammals), are generally rich in viable (i.e., capable of activity) and active TEs, whereas nonfecund lineages (e.g., monotremes) have mainly nonviable (i.e., incapable of activity) and inactive TEs. Evolutionary transitions, for example, the evolution of the higher primates and evolutionary innovations, such as the mammalian placenta, also appear to be facilitated by TEs (Oliver and Greene 2011). An outline of the TE-Thrust Hypothesis is:
Many eukaryote lineages are able to tolerate some sacrifices in the present, that is, a genomic “load” or population, of mostly controlled, but possibly fitness-reducing TEs. Such lineages may, thereby, fortuitously, gain a continuum of “intra-genomic potential” whose extremities are conveniently described as “adaptive potential” and “evolutionary potential.” This intragenomic potential may be realized in the present, and/or in the descendant lineage(s) of the future. Note that this does not imply any “aim” or “purpose” to evolution, or any ability of evolution to “see” into the future.
As environmental or ecological factors change, or the lineages adopt new habitats, these intragenomic potentials can be realized. For example, adaptive potential can be realized to give small adaptive changes within a lineage, over short periods of time, such as the evolution of insecticide resistance, when insecticides become prevalent in the environment. Evolutionary potential can be realized, over much longer periods of time, perhaps in adaptive radiations, as in some rodents or bats.
At least some unicellular eukaryotic organisms do not appear to tolerate a genomic load of TEs (Galagan and Selker 2004; Pritham 2009), which suggests that TE-Thrust does not operate in all extant biological lineages. However, it is noteworthy that most eukaryotic species known to lack TEs are intracellular parasites with small genomes, including members of the Babesia, Cryptosporidium, and Plasmodium genera (Pritham 2009). This could be due to selection for small cell size and/or because the genomic plasticity engendered by TEs may not provide a net advantage to nonfree-living organisms that exist within a stable environment.
TE-Thrust and Punctuated Equilibrium
Eldredge and Gould (1972) posed the concept of punctuated equilibrium from studies of the fossil record, as opposed to the then prevailing concept of phyletic gradualism. There is now independent support for punctuated equilibrium from studies of extant taxa (Cubo 2003; Pagel et al. 2006; Mattila and Bokma 2008; Laurin et al. 2012), from co-evolution (Toju and Sota 2009), and in extant and ancient genomes of Gossypium species due to intermittent TE activity (Palmer et al. 2012). TE-Thrust provides an intragenomic explanation of punctuated equilibrium (Oliver and Greene 2009a,b, 2011), as has also been suggested by Zeh et al. (2009), via epigenetic changes, and/or endogenization of retroviruses, in response to stress, and Parris (2009), via endogenization of retroviruses and environmental change.
The actual processes of speciation events seem to be poorly understood, but new species are said to emerge from many differing and rare single events (Venditti et al. 2010). However, two almost essential components seem to be necessary: reproductive isolation and intragenomic variation. Of these, intragenomic variation can be readily supplied by the hypothesized TE-Thrust (Oliver and Greene 2011), and reproductive isolation can be provided by a variety of means, including karyotypic changes, polyploidy, hybridization, and physical environmental or ecological factors (Venditti et al. 2010).
Much TE activity (active TE-Thrust) is thought to occur in intermittent bursts that interrupt more quiescent periods of low activity (Bénit et al. 1999; Marques et al. 2005; Cantrell et al. 2005; Pritham and Feschotte 2007; de Boer et al. 2007; Ray et al. 2008; Zeh et al. 2009; Erickson et al. 2011). These punctuation events can occur especially after intermittent infiltrations or amplifications of TEs. New acquisitions of TEs can be due to:
Intermittent horizontal transposon transfer (HTT) (Schaack et al. 2010). This appears to be relatively rare, and probably tends to occur more often with some DNA-TEs, LTR retro-TEs, and the Bov-B LINE.
The de novo synthesis of chimeric elements, for example, the hominid specific SVA (Wang et al. 2005). This is probably rare.
The de novo syntheses of various SINEs, the younger ones (<100 Myr) of which are lineage specific (Piskurek et al. 2003; Kramerov and Vassetzky 2011). This is probably rare.
Intermittent endogenizations of various RNA viruses (Bénit et al. 1999; Belyi et al. 2010; Horie et al. 2010). This may be relatively common, especially in mammals.
Hybridization, especially in angiosperms (Michalak 2010). This appears to be common.
Intermittent de novo modifications to successive families of TEs (e.g. L1 LINEs). This is relatively common.
An example of an intermittent burst is the L1 LINE in ancestral primates, where among a large number of overlapping families, L1PA6, L1PA7, and L1PA8 were apparently amplified intensively around 47 Mya. This seemingly contributed to a very large Alu SINE, and retrocopy, amplification at this time (Ohshima et al. 2003). TEs can result in the acceleration of the evolution of genes in a myriad of ways (Böhne et al. 2008; Goodier and Kazazian 2008; Hua-Van et al. 2011), providing a means for rapid species divergences in the affected lineages.
Modes of TE-Thrust
All the hypothesized modes of TE-Thrust shown below are consistent with the data tabulated in Oliver and Greene (2011), but are expressed herein in different ways. All of them refer only to the potential for adaptation or evolution due to the hypothesized TE-Thrust. As other facilitators of evolution will possibly also be active in addition to TE-Thrust, and as environmental and ecological factors can frequently change, all these hypothesized capabilities of TE-Thrust need to be predicated by “if all else is equal”. These modes of TE-Thrust are extremes of continuums, so intermediate modes must occur.
Mode 1. Evolutionary potential may be realized, in concert with, or following, significant intermittent bursts of TE activity, in viable and heterogeneous TE populations, whether large or small. This can underlie what we designate as “Type I” punctuated equilibrium (stasis with punctuation events), due to intermittent active TE-Thrust.
Mode 2. Evolutionary potential may be realized, in concert with, or following, significant bursts of TE activity, in large viable and homogenous TE populations. This can result in what we designate as “Type II” punctuated equilibrium (gradualism with punctuation events) due to both ongoing TE-Thrust (largely passive), and to intermittent active TE-Thrust. If the TE population is small, then only intermittent active TE-Thrust is likely to occur as per mode 1.
Mode 3. Nonviable heterogeneous TE populations, whether large or small, may result in evolutionary stasis, due to a lack of both active and passive TE-Thrust.
Mode 4. If a nonviable TE population is both large and homogeneous, and not too degraded by mutations, then gradualism type evolution may occur, due largely to passive TE-Thrust. If the TE population is small, then little TE-Thrust is likely to occur as per mode 3.
An Expansion of the TE-Thrust Hypothesis
Herein, the TE-Thrust hypothesis is further expanded from its original formulation. We acknowledge that in addition to TE-Thrust, other nongenomic facilitators of evolution may play a part in radiations and evolution, such as dynamic external factors, including geological, environmental, and ecological changes. Such factors may result in fragmentation of populations into small local demes, or larger disjunct sub-populations, which can result in reproductive isolation with possible divergence into novel taxa (Wright 1931; Eldredge 1995; Jurka et al. 2011). In addition to alleles drifting to fixation or extinction in demes, TE families likely also do so (Jurka et al. 2011) and we are in agreement with this. Additionally, in TE-Thrust we hypothesize that novel TEs as described above, may very occasionally be introduced into, or arise within, some demes or disjunct populations, but not into others, ultimately causing evolutionary transitions or the evolution of new taxa. We view the carrier subpopulation (CASP) hypothesis (Jurka et al. 2011) to be complementary to TE-Thrust, as it is about the fixation of TEs in populations and the details of mechanisms, or origins, of speciation, which were previously not included in the TE-Thrust hypothesis. The CASP hypothesis gains some support from the cotton genus (Gossypium) specific Gorge retro-TEs (Palmer et al. 2012), as Gorge seems to have spread to fixation in a small progenitor population of Gossypium. Indeed, both hypotheses are in agreement in strongly relating TEs to speciation and evolution. However, we suggest that karyotypic changes due to TE presence and activity, are among the factors that produce the reproductive isolation necessary for speciation, although we agree that geographic isolation into demes, niche availability, and many other phenomena (e.g., pheromone changes in insects) are also important factors.
We note that adaptive evolution via natural selection is, but one of the forces of evolutionary change. Other important forces, all of which are nonadaptive, comprise mutation, recombination, and random genetic drift (Lynch 2007). As TE-Thrust emphasizes a key intragenomic role for TEs in mutation and recombination, it fits comfortably with a growing body of evidence indicating that a significant portion of evolutionary changes are not adaptive in nature, but result from the accumulation of mildly deleterious mutations that can become fixed by genetic drift in populations of relatively small size (Fernández and Lynch 2011). Indeed, although the occasional highly deleterious TE insertion will be rapidly culled by purifying selection, TE insertions can themselves be viewed overall as an accumulation of neutral to mildly deleterious mutations that are subject to genetic drift. Activation of TEs, for example, during stress, or horizontal transfer of TEs etc., provides powerful complements to genetic drift. Thus, TEs accumulate by nonadaptive processes and can underpin nonadaptive change, and they also readily provide the raw material for future beneficial traits capable of undergoing positive selection.
We recognize that there are many known genomic facilitators of evolution, besides TE-Thrust. A few apposite examples are: symbiosis (Ryan 2007, 2009); hybridization (Ryan 2006; Larsen et al. 2010); noncoding RNA (Heimberg et al. 2008; Mattick 2011); horizontal gene transfer (Richards et al. 2006); whole genome duplications (Hoffmann et al. 2012), and viral driven evolution (Villarreal 2005, 2009; Ryan 2007; Villarreal and Witzany 2010; Feschotte and Gilbert 2012). Some facilitators of evolution may have greater importance in some clades than in others. For example, whole genome duplication (polyploidy) is apparently quite important in the evolution of angiosperms (Soltis et al. 2004). Ryan (2006) includes several of the examples above under the general descriptor “genomic creativity”.
Horizontal Transfer of TEs in TE-Thrust
Mobile DNA has been classified into Class I retro-TEs (e.g., LTR elements, LINEs, and SINEs), and Class II DNA-TEs, composed of subclasses 1 (e.g., Tc1-Mariner and hAT) and 2 (Helitron and Maverick), as have been described and reviewed elsewhere (Wicker et al. 2007; Böhne et al. 2008; Goodier and Kazazian 2008; Kapitonov and Jurka 2008; Hua-Van et al. 2011). The horizontal transfer of TEs (horizontal transposon transfer or HTT) has previously been proposed as a major force driving genomic variation and biological innovation (Schaack et al. 2010). DNA-TEs have long been known to be capable of HTT, for example, the P-element DNA-TE in Drosophila (Anxolabéhère et al. 1988; Daniels et al. 1990); the Mariner DNA-TE in various insects (Maruyama and Hartl 1991; Robertson and Lampe 1995; Lampe et al. 2003), and DNA-TEs in the bat Myotis lucifugus (Pritham and Feschotte 2007; Ray et al. 2007). However, HTT of retro-TEs, has been less well documented, except for some examples, including the patchily distributed Bov-B LINE, (Kordiš and Gubenšek 1998; Gogolevsky et al. 2008) and the Gypsy-like retro-TEs (Herédia et al. 2004).
Although probably infrequent, HTT is an important aspect of the TE-Thrust hypothesis that has so far only been given cursory attention (Oliver and Greene 2009a, 2011). Over 200 cases of HTT have been documented (Schaack et al. 2010), 12 of which were between different phyla. About a half of these known HTTs involved retro-TEs, most of which were LTR retro-TEs. The remaining HTTs involved a variety of DNA-TEs. Horizontal transfer is an important part of the life cycle of TEs, as they generally accumulate mutations and eventually become nonviable in the genomes they occupy. This can downgrade the efficacy of TE-Thrust. However, they are sometimes enabled, via chance events, to periodically make fresh starts with fully functional elements, in the genomes of other lineages. At least some TEs appear to be able to endure in the absence of HTT. For example, the LINE 1 (L1) retro-TE in mammals has persisted for 100 Myr with no known evidence of HTT (Furano et al. 2004; Khan et al. 2006), although it has now become nonviable in a few mammalian lineages (Casavant et al. 2000; Boissinot et al. 2004; Cantrell et al. 2008; Platt and Ray 2012).
Viruses and bacteria appear to be likely vectors of HTT (Piskurek and Okada 2007; Schaack et al. 2010; Dupuy et al. 2011), but endoparasites and intracellular parasites are among other possible vectors that have been proposed (Silva et al. 2004; Schaack et al. 2010). Empirical data (Anxolabéhère et al. 1988; Cantrell et al. 2005; de Boer et al. 2007; Pritham and Feschotte 2007; Ray et al. 2008) and simulations (Le Rouzic and Capy 2005) both suggest that TE amplification occurs immediately after HTT of a viable TE copy.
Holobionts and Holobiontic Genomes, and The Importance of the Highly Mobile Retroviruses
Exogenous retroviruses can become endogenized, and can be united with the host genome into a holobiontic genome in a new holobiont (Box 1). Holobiont is a symbiological term that means the partnership, or union, of symbionts (Rosenberg et al. 2007; Ryan 2007; Gilbert et al. 2010). For example, the ERVWE1 locus in the human genome comprises a conserved envelope (env) gene together with the conserved 5′ LTR of a retrovirus that contains regulatory elements. This locus, additionally, includes sections of human genetic sequences and these also play a role in regulation of the env gene, which codes for Syncytin-1 (Mi et al. 2000). Syncytin-1 has a crucial function in trophoblast cell fusion in ape placental morphogenesis (Mi et al. 2000), which strongly suggests that selection has occurred at the level of the holobiontic genome in the human plus retrovirus holobiont (Ryan 2006).
Retroviruses appear to be the most mobile of all “mobile DNA” as they can exist exogenously as infectious, or persisting viruses, as well as by becoming endogenized in host germ lines (Hughes and Coffin 2001, 2004; Ryan 2006). Exogenous retroviruses are distinct entities to those species whose genomes into which they endogenize to become an ERV, and they have an extracellular or virion stage, with a protein capsid. ERVs then are a part of a holobiont organism. Other TEs in a genome are not considered to be a part of a holobiont, as they seemingly can only transfer from genome to genome, and can have no independent existence like that of an exogenous retrovirus species.
Endogenized retroviruses (ERVs) can multiply within a genome either by repeated endogenizations, or by retrotransposition within the genome (Belshaw et al. 2004; Wang et al. 2010). Over time, due to recombinations between their LTRs, and deletions, ERVs often exist mostly as solo LTRs or sLTRs, (Sverdlov 1998). Many Class I elements are related to retroviruses, namely the Copia, Gypsy, and BEL/Pao subclasses of LTR retro-TEs, which have LTRs (long- terminal repeats), but lack an env gene.
Retroviruses are present among all placental mammals (Bénit et al. 1999), are largely restricted to vertebrates, and are particularly abundant in mammals (Villarreal 2005). Retroviruses have been endogenized in mammalian germ lines many times during the evolution of mammals. These ERVs have been a very important factor in their evolution (Villarreal 2005), and are particularly associated with that mammalian innovation, the placenta (Oliver and Greene 2011). Endogenized retroviruses, and the role they play in evolution, have been extensively detailed elsewhere (Villarreal 1997, 2004, 2005, 2009; Ryan 2003, 2006, 2007; Feschotte and Gilbert 2012).
Endogenous nonretroviral RNA virus elements, notably Bornaviruses, have also been found in mammalian genomes, including several primates and several rodents, and these viral sequences appear to have function (Belyi et al. 2010; Horie et al. 2010). Indeed, all major types of eukaryotic viruses can give rise to endogenous viral elements or EVEs (Feschotte and Gilbert 2012). Thus, viral-eukaryote holobiont organisms appear to be not uncommon, and these could have lead to significant evolutionary innovation. This enhances the explanatory power of the TE-Thrust hypothesis.
Retroviruses and the Evolution of the Mammalian Placenta
The placenta represents a major evolutionary innovation that occurred over 160 Mya at the time of the divergence of the placental mammals. The circulatory and the metabolic benefits provided by this transient organ to the growing embryo and fetus have been well investigated, but less so well understood is the origin of the placenta. The invasive syncytial plate, the precursor to the placenta, and the rapidly growing trophoblast, are developmentally unique to mammals (Harris 1991). Harris proposes that prior to the divergence of placental mammals, developing embryos became infected at an early intrauterine stage with retroviruses, which gave rise to cellular proliferation and creation of the trophoblast. This may then have resulted in the formation of the highly invasive “tumor-like” vacuolated and microvillated syncytial plate and a primitive placenta (Harris 1991). Although to date, there is no proof that the fusogenic ERVs of premammals resulted in the evolution of the mammalian placenta (Harris 1991; Dupressoir et al. 2009) it seems likely to be correct. Supporting evidence comes from the egg-laying platypus, which has a genome that is devoid of ERVs, although there are some thousands of ancient Gypsy-class LTR retro-TEs (Warren et al. 2008). In contrast, all examined placental mammal genomes do contain many ERVs (Mayer and Meese 2005; Villarreal 2005), with ERV/sLTRs constituting approximately 8% and 10% of the human and mouse genomes, respectively (Waterston et al. 2002). Atypically, the placenta exhibits global DNA hypomethylation, which allows many ERVs and retro-TEs to retain transcriptional activity in this tissue (Rawn and Cross 2008). Such a permissive environment for expression of TEs facilitates their exaptation as coding or regulatory sequences, and indeed, the LTRs of ERVs contain promoter activity that can confer tissue-specific expression in the placenta, as for example, the CYP19A1, IL2RB, NOS3, and PTN genes, which are solely expressed by an LTR promoter (Cohen et al. 2009). Although there are few known unique placenta-specific genes, numerous genes expressed in the human placenta are derived from retro-TEs and ERVs (Rawn and Cross 2008). Most notable are the fusogenic, ERV env-derived, syncytin-1, and syncytin-2 (Mi et al. 2000; Blaise et al. 2003), with syncytin-2 also having an immunosuppressive function (Kämmerer et al. 2011). The efficient adaptive immune systems of mammals must fail to initiate an immune reaction to the antigens of their embryos and placentas, and mammals alone are very highly infected with the generally immunosuppressive endogenous retroviruses (Villarreal 1997). Intriguingly, retroviruses are abundant around sperm heads and also coat the female placenta (Steele 2009). The advantages of the placenta could possibly explain why extant placental mammals number well over 5,000 species, whereas there are less than 300 extant species of marsupials (Pough et al. 2009).
Evolvability and the TE-Thrust Hypothesis
Mutation, including gene duplication and other DNA changes, is the driving force of evolution at both the genic and the phenotypic levels (Nei 2005, 2007). Significantly, Shapiro (2010) proposes that it is mobile DNA movement, rather than replication error that is the primary engine of protein evolution. Along the same lines, Hua-Van et al. (2011) stress TEs as a major factor in evolution, whereas Muotri et al. (2007) proposes that “handy junk” can evolve into “necessary junk”. Wagner (Heard et al. 2010), in support of our original concepts (Oliver and Greene 2009a) states that, in general, “the kinds of genetic changes that are possible depend on what kinds of TEs are present and active at any particular time”, in the evolution of each lineage. Thus, the potential for evolutionary innovations differs over time, contradicting the concept of gradualism in lineages. Caporale (2009) posits that “selection must act on the mechanisms that generate variation, much as it does on beaks and bones”. Earl and Deem (2004), with no mention of TEs, propose the evolution of mechanisms to facilitate evolution, and describe evolvability as a selectable trait. Further to this, Woods et al. (2011) found experimental evidence, in a study of bacteria that long-term evolvability may be important for determining the ultimate success of a lineage, and that less fit lineages with greater evolvability may eventually out-compete lineages with greater fitness. All these lines of reasoning, and associated experimental data, are in good accord with the TE-Thrust hypothesis.
Reduced “Fitness” versus enhanced “Adaptive Potential” and “Lineage Selection”
Accumulation of TEs in the genome of Drosophila melanogaster has been found to be associated with a decrease in fitness (Pasyukova et al. 2004). The reduced “fitness” in Drosophila may be an extreme case, because in D. melanogaster TEs cause over 50% of de novo mutations (Pasyukova et al. 2004). In contrast to D. melanogaster, de novo disease-causing insertions in humans are relatively rare (Deininger and Batzer 1999; Kazazian 1999; Chen et al. 2005; Hedges and Batzer 2005), whereas TE activity in the laboratory mouse falls between these two extremes (Kazazian 1998; Waterston et al. 2002; Maksakova et al. 2006). There is, however, no conflict with the TE-Thrust hypothesis with this finding in Drosophila, as despite a fitness loss in some individuals in the present, there can be a fortuitous gain in adaptive potential to the lineage as a whole. TEd-alleles (TE- deactivated or destroyed alleles), for example, usually lower the fitness of the lineage. However, TEm-alleles (TE-modified alleles, which can be modified in either regulation or function, or duplicated), for example, increase the genetic diversity, and hence the adaptive potential, of the lineage. These TEm-alleles allow the lineage to adapt to environmental/ecological challenges in the present. Also, importantly, this adaptive potential may be latent in the present, and only be realized in the future, as environmental/ecological challenges change. This latent adaptive potential then, increases the chances of the long-term survival of the lineage. In other words, TE-Thrust can result in latent adaptive potential (also called standing variation), which can be realized, if needed, in the future, and can result in the differential survival of lineages. This is the rationale for positing lineage selection in the TE-Thrust hypothesis (Oliver and Greene 2009a,b, 2011).
Realizable “Adaptive Potential” Due to TE-Thrust
TE-Thrust is proposed to have facilitated adaptive change, as we highlighted in the simian lineage (Oliver and Greene 2011). The ongoing ability of TEs to provide realizable adaptive potential is illustrated by TE-generated polymorphic traits identified in isolated populations of laboratory-bred mice (Table 1), as well as by structural variation in the human genome still being created by L1 activity (Ewing and Kazazian 2010).
[...]A specific example of an adaptive benefit from TE activity is the development of insecticide resistance in the Hikone-R strain of Drosophila melanogaster. [...] These four steps have occurred within 70 years in the Hikone-R strain of Drosophila melanogaster, and the more derived the allele, the greater the resistance (Schmidt et al. 2010). Such allelic successions, whereby different adaptive alleles are substituted sequentially have been demonstrated in several other studies of insecticide resistance (Schmidt et al. 2010).[...]
The Failure of Mutation Breeding
In a review, Lönnig (2005), described how, despite early enthusiasm and sustained effort, mutation breeding (in either plants or animals) has never been successful. The mutations caused by mutagens usually produced weaker or nonfunctional alleles of wild type genes. In TE-Thrust, however, the TEs usually consist of functional coding or exaptable sequences, and often also of potent regulatory sequences, so that by insertion and in many other ways, for example, exon shuffling in the active mode and ectopic recombination in the passive mode, they can make many beneficial changes, although they may sometimes do damage (Oliver and Greene 2009a,b, 2011). TEs can alter the regulation or the structure of alleles, or duplicate them (Darboux et al. 2007; González et al. 2009, 2010; Schmidt et al. 2010) creating TEm-alleles. Therefore, although attempted breeding, adaptation or evolution, using mutagens to generate alternative alleles almost always does not work (Lönnig 2005), adaptation or evolution using TE-Thrust generating TEm-alleles relatively often does work. This is not to say that other types of mutation, such as point changes, are not important in evolution. In fact, in addition to their general importance in evolution, such mutations often complement TE-Thrust, for example, by modifying TE-duplicated sequences.
Reduced “Fitness” versus Enhanced “Evolutionary Potential”
The question of whether or not the possible lowering of fitness in a lineage by TEs can result in enhanced evolutionary potential may be simplified into two competing hypotheses:
The Null Hypothesis: TE-Thrust is not causal to adaptation, speciation, punctuation events, or evolution.
The Alternative Hypothesis: TE-Thrust is causal to adaptation, speciation, punctuation events, and evolution.
Testing the Hypotheses
Recent/ancient speciation and the alternative (TE-Thrust) hypothesis
In the absence of events, such as intermittent de novo modifications to successive families of TEs, de novo SINE synthesis, HTT, or de novo synthesis of chimaeric TE elements, TE bursts in lineages eventually tend to fade to inactivity, with TEs becoming nonviable and degraded by the accumulation of deleterious mutations. An example is the apparent loss of L1 element activity in a number of species. These include the spider monkey, thirteen-lined ground squirrel, megabats, and sigmodontinae rodents (Casavant et al. 2000; Boissinot et al. 2004; Cantrell et al. 2008; Platt and Ray 2012), although at least in the case of the sigmodontinae, which have undergone rapid fecund speciation with numerous karyotypic changes, the loss of viable LINEs appears to have been more than compensated for by massive endogenisations of ERVs (Cantrell et al. 2005; Erickson et al. 2011). As TE-Thrust predicts that lineages lose their adaptability as overall TE activity and integrity fades, the loss of TE viability over time provides an intragenomic explanation to help account for the high rate of background extinction that has been a prevalent feature of life on earth (Raup 1994). In contrast, lineages harboring young TE families are associated with recent speciation. This is well exemplified in the mammals where species with the highest numbers of young TE families, such as the mouse, rat, bat, rhesus macaque, and human, represent the largest extant mammalian orders of rodents, bats, and primates (Jurka et al. 2011). Very species-poor extant mammalian lineages, such as the alpaca, elephant, tenrec, armadillo, and platypus, do not harbor any young families of TEs (Jurka et al. 2011). Nevertheless, TE-Thrust predicts more ancient speciation events being attributed to older families of TEs, when they were young, and this is supported by phylogenetic analyses (Jurka et al. 2011). These data are consistent with the Alternative (TE-Thrust) Hypothesis.
The vesper bats and the alternative (TE-Thrust) hypothesis
The radiation of the vesper bats (family Verspertilionidae) appears to support the Alternative Hypothesis and the active mode of TE-Thrust. The vesper bats, which have an almost worldwide distribution (Nowak 1994), are a fecund lineage (407 species of the approximately 930 species of microbats or 8–9% of all extant mammal species), and include Myotis, the most speciose mammalian genus with about 103 members. Significantly, vesper bats are somewhat unique in having many viable and active DNA-TEs that have been nonviable in most other mammals for 37 Myr (Pace and Feschotte 2007).
The early radiation of the vesper bats is proposed to have been due to HTT of Helitron DNA-TEs, called Helibat, into the vesper bat lineage about 30–36 Mya (Pritham and Feschotte 2007).
Amplification of DNA-TEs is thought to follow HTT in a naive lineage, which can result in innovations in the genome (Pace et al. 2008).
Helibat has amplified explosively up to at least 3.4% of the Myotis lucifugus genome (Ray et al. 2008).
HTT of Helitrons, especially, can lead to diversification, and to dramatic shifts in the trajectory of genome evolution (Thomas et al. 2010).
HTT of of DNA-TEs can also lead to horizontal gene transfer (Thomas et al. 2010).
Although Helitrons have not been detected in other mammals besides the vesper bats, they are abundant in plants, invertebrates, and zebrafish, and have been implicated in large-scale gene duplication and exon shuffling.
There were other multiple waves of HTT of DNA-TEs in the bat lineage coinciding with a period of their rapid diversification 16–25 Mya (Teeling et al. 2005; Pritham and Feschotte 2007; Ray et al. 2008).
A further burst of New World Myotis diversification 12–13 Mya was noted (Stadelmann et al. 2007), corresponding well with the period that the most active transposition of a variety of DNA-TEs is estimated to have occurred (Ray et al. 2008).
Such repeated waves of TE activity suggest a mechanism for generating the genetic diversity needed to result in the evolution of such great species richness as is observed in the vesper bats (Ray et al. 2008).
Active retro-TEs, namely L1 LINEs (Cantrell et al. 2008) and VES SINEs (Borodulina and Kramerov 1999), have also been found in vesper bats.
This mix of viable DNA-TEs and retro-TEs, unknown in other mammals, could have resulted in large architectural and organizational changes in their genomes and aided in the Myotis diversification, enabling adaptation to very diverse ecological niches within this lineage (Pritham and Feschotte 2007; Thomas et al. 2011). This suggests that much active TE-Thrust has operated during the very large radiation of the vesper bats during the last 36 Myr. A lack of data presently obscures any conclusions regarding any possible involvement of passive TE-Thrust. The predicted evolutionary outcome of such intermittently active populations of TEs is either gradualism or stasis with punctuation events, (Type I or II punctuated equilibrium). Current data suggest that this is correct for the Verspertilionidae.
The Muridae Rodents and the Alternative (TE-Thrust) Hypothesis
The extensive radiation of the Old World Muridae (the Murinae) appears to support the Alternative Hypothesis, and both the active and the passive modes of TE-Thrust. The rodents are the most fecund mammalian order comprising about 40% of mammals with an almost worldwide distribution. The Muridae family, which include the true mice and rats, have been particularly successful and account for about two-thirds of all rodent species. Representatives of the subfamily Murinae (Mus and Rattus) possess large populations of relatively homogenous retro-TEs, many of which are viable and active (Table 2).
Table 2
Table 2
Presence and Viability of Transposable Elements (TEs) in Distinct Mammalian Species
The Old World mouse (Mus) and rat (Rattus), with some 50–60 species each in their respective genera, have genomes comprised of about 40% largely homogenous genomic TEs. These include numerous viable and mostly highly active L1 LINEs and few nonviable ancient L2 LINEs, giving a LINE total of 22%. SINEs comprise a further 7% and most (92%) are lineage specific, viable, and effective, although slightly diverse, with only few being the nonviable ancient MIR SINEs. Less than 1% of their genomes are composed of nonviable DNA-TEs (Waterston et al. 2002; Gibbs et al. 2004). The mouse has about 10% ERV/sLTRs, many of which are very active and are closely related to mouse exogenous retroviruses (Maksakova et al. 2006).
The fitness cost of their greatly enhanced evolutionary potential is higher than in humans, as previously noted (Maksakova et al. 2006).
Although the generally small size of many rodents probably aided in their diversification, there has seemingly been much active TE-Thrust, as indicated by the growing number of documented examples of rodent-specific traits generated by TEs (Table 3). They are also quite well suited to passive TE-Thrust, as they have large homogenous populations of TEs to facilitate TE-mediated duplications, inversions, deletions or karyotypic changes. The predicted evolutionary outcome of large homogenous and intermittently active populations of TEs is gradualism with punctuation events (Type II punctuated equilibrium), as in the hypothesized mode 2 of TE-Thrust.
Table 3
Table 3
Specific Examples of Transposable Elements (TEs) Implicated in Rodent-Specific Traits
The naked mole rat and the alternative (TE-Thrust) hypothesis
In sharp contrast to Mus and Rattus, which are both very rich in species and have abundant viable and active TEs (Waterston et al. 2002; Gibbs et al. 2004), the rodent genus Heterocephalus, also in the family Muridae, has only one species (Wilson and Reader 2005). In support of the Alternative Hypothesis, sequencing of H. glaber (Kim et al. 2011), the very atypical, physiologically unique, eusocial, and long-lived naked mole rat, has shown that it possesses a nonviable and relatively small mobilome consortium (Table 2).
The TEs of the naked mole rat, although they are homogenous and constitute 25% of the genome, are highly divergent, indicating they have been both nonviable and inactive for a very long time (Kim et al. 2011).
As most mammals have 35–50% TEs, this suggests that a substantial portion of its TEs may have been lost altogether.
The data indicate that H. glaber has had little or no TE-Thrust, except in the remote past, and if all else is equal, it is in stasis or gradualism. (Note: As viable and active TEs are known to occasionally cause harmful mutations, these data additionally suggest that there possibly could be less genetic disease and cancer in the individuals of species, such as H. glaber).[...]
Summary of the evidence for the alternative (TE-Thrust) hypothesis
It can, of course, be argued that this evidence in mammals (microbats, rodents, and the platypus), reptiles (the green anole lizard and the tuatara), and the evolution of the mammalian placenta, is all only circumstantial evidence, and therefore does not demonstrate a causal link between TE-Thrust and enhanced evolutionary potential. This argument is weakened by the abundance of young families of TEs in the largest extant mammalian orders of rodents, bats, and primates, and their absence in the elephant, alpaca, tenrec, armadilo, and platypus. The argument of “only circumstantial evidence” is further weakened by the wide range of known conserved and/or beneficial genomic modifications that are due to TEs in various lineages (Brosius 1999; Miller et al. 1999; Kidwell and Lisch 2001; Nekrutenko and Li 2001; van de Lagemaat et al. 2003; Jordan et al. 2003; Kazazian 2004; Shapiro and Sternberg 2005; Volff 2006; Böhne et al. 2008; Oliver and Greene 2009a, 2011). Therefore, it seems that a causal link between recent TE activity, sometimes resulting in reproductive isolation, and recent speciation events is indeed likely.
Some hard evidence can be provided with regard to adaptive potential and adaptive evolution in insecticide resistance by insects in the last 70 years, and adaptation to temperate climates in the last few centuries. However, a punctuation event is estimated to take between 15,000 and 40,000 years (Gould 2002). It appears then that, as yet, bursts of TE activity and punctuation events cannot be dated accurately enough to establish any definite relationship. However, some apparent correlations have been reported, suggesting that increased TE activity may indeed be basal to, or coincident with, punctuation events and evolutionary transitions, speciation, or large radiations. Some examples of these, in addition to those detailed above, are:
Ohshima et al. (2003) found bursts of Alu SINE and retrocopies coincident with the radiation of the higher primates 40–50 Mya.
DNA-TE activity coincided with speciation events in salmonoid fishes (de Boer et al. 2007).
Bursts of transposition of BS element transposition have also shaped the genomes of at least two species of Drosophila, D. mojavensis and D. recta (Granzotto et al. 2011).
There are numerous examples of bursts of TE activity that often follow polyploidization events (Comai 2000), or hybidization (Michalak 2010), in angiosperms, leading to speciation.
Some suggest that a role for TEs in speciation is speculative (Hua-Van et al. 2011), whereas others have given data, which they readily acknowledge specifically suggests TE involvement in taxon radiations (de Boer et al. 2007; Pritham and Feschotte 2007; Ray et al. 2008; Thomas et al. 2011). In our interpretation of the available data, we suggest that, if all else is equal, minimal or passive TE-Thrust is likely to result in stasis or gradualism, whereas active TE-Thrust is likely to be causal to innovative evolution (e.g., the placenta), punctuation events and radiations, as in our hypothesized four modes of TE-Thrust (Oliver and Greene 2011). However, we readily acknowledge that some punctuation events may be caused by other facilitators of evolution.
Conclusions
The field of evolutionary biology has seemingly paid more attention to the outcomes of genetic mutation in terms of the generation of variants and their selection within populations than the mechanisms by which mutations emerge in the first place. Although small-scale DNA base changes and deletions are important in evolution, TEs (and viruses) are uniquely placed, via TE-Thrust, to expeditiously cause complex and/or large-scale changes and thereby help explain macroevolutionary change and the emergence of highly innovative adaptations. Much still remains to be investigated, such as the relevance of TE-Thrust to other classes and phyla. Only a small number of lineages in the metazoans: the mammals and to a lesser extent, a very few lineages of the insects, plants, and reptiles, have been considered with regard to the TE-Thrust hypothesis to date. As increasing numbers of genomes are being sequenced, it would be interesting to investigate the link between TEs, exogenous viruses, and enhanced adaptive potential, enhanced evolutionary potential, evolutionary transitions, and the occurrence of punctuation events, in the lineages of other taxa. It seems likely that in the great diversity of extant lineages, TE-Thrust and other facilitators of evolution will have had a greater or lesser impact on adaptation and evolution. There seems to be little doubt, however, that TEs and viruses have played a major and prominent role in the evolution of almost all life on earth, and that TEs and viruses need to be recognized and included, as the TE-Thrust hypothesis, in a much needed extension and modification in evolutionary theory.
This is a publication of the journal Nature. It is very mainstream, yet one gets the idea that something is going on in the Virology world that has them working around the clock so to speak. It is the second publication I had stumbled upon among these lines that has open access.
I think they are genuinely worried. But they should be reading the signs of the times and looking up to the sky for more clues :D
I think they are genuinely worried. But they should be reading the signs of the times and looking up to the sky for more clues :D
Anthony said:
I think that is even more telling. The Black Death was caused by an Ebola-LIKE virus, not necessarily Ebola itself. I suspect that any newly inborn-cometary virus would be precisely that, completely new and not necessarily detected by standard lab analysis, unless they look harder. That is, if Ebola analysis comes back negative, then we are talking about some kind of virus that scientists don't have a hold of yet, but still produces an hemorrhagic fever just like the Black Death did.
This can be the beginning, not necessarily THE return of the black death, but I wouldn't be surprised if one of these days we meet a global outbreak of unprecedented proportions in modern history.
My 2 cents!
The fatality rates of these hemorrhagic fever causing viruses are astounding. We'll have to wait and see what's in store.
I can imagine this virus taking space more and more and all West Africa been touched. This can be terrible.
Some years ago Richard Preston wrote a book about a virus very similar of the Ebola.
http://www.amazon.com/The-Hot-Zone-Terrifying-Story/dp/0385479565/ref=sr_1_1?ie=UTF8&qid=1395838066&sr=8-1&keywords=the+hot+zone
Some years ago Richard Preston wrote a book about a virus very similar of the Ebola.
http://www.amazon.com/The-Hot-Zone-Terrifying-Story/dp/0385479565/ref=sr_1_1?ie=UTF8&qid=1395838066&sr=8-1&keywords=the+hot+zone
Al Today
The Living Force
The Hot Zone shows how terrifyingly easy the world can become infected on a global scale just by someone taking an international plane ride. A person merely walking through the hallways of an international airport where one person breathes someones air, passes the bugger along to another, along to another and along on and on. Within minutes. People in the hallway get infected then disburse to their different global destinations, just to give a gift that keeps giving. Like a geometric progression or a wave perhaps... It's not easy to wrap my head on how quickly the world can become a petri dish.
