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Horizontal gene transfer: essentiality and evolvability in prokaryotes, and roles in evolutionary transitions
The wide spread of gene exchange and loss in the prokaryotic world has prompted the concept of ‘lateral genomics’ to the point of an outright denial of the relevance of phylogenetic trees for evolution. However, the pronounced coherence congruence of the topologies of numerous gene trees, particular...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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F1000Research
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962295/ https://www.ncbi.nlm.nih.gov/pubmed/27508073 http://dx.doi.org/10.12688/f1000research.8737.1 |
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author | Koonin, Eugene V. |
author_facet | Koonin, Eugene V. |
author_sort | Koonin, Eugene V. |
collection | PubMed |
description | The wide spread of gene exchange and loss in the prokaryotic world has prompted the concept of ‘lateral genomics’ to the point of an outright denial of the relevance of phylogenetic trees for evolution. However, the pronounced coherence congruence of the topologies of numerous gene trees, particularly those for (nearly) universal genes, translates into the notion of a statistical tree of life (STOL), which reflects a central trend of vertical evolution. The STOL can be employed as a framework for reconstruction of the evolutionary processes in the prokaryotic world. Quantitatively, however, horizontal gene transfer (HGT) dominates microbial evolution, with the rate of gene gain and loss being comparable to the rate of point mutations and much greater than the duplication rate. Theoretical models of evolution suggest that HGT is essential for the survival of microbial populations that otherwise deteriorate due to the Muller’s ratchet effect. Apparently, at least some bacteria and archaea evolved dedicated vehicles for gene transfer that evolved from selfish elements such as plasmids and viruses. Recent phylogenomic analyses suggest that episodes of massive HGT were pivotal for the emergence of major groups of organisms such as multiple archaeal phyla as well as eukaryotes. Similar analyses appear to indicate that, in addition to donating hundreds of genes to the emerging eukaryotic lineage, mitochondrial endosymbiosis severely curtailed HGT. These results shed new light on the routes of evolutionary transitions, but caution is due given the inherent uncertainty of deep phylogenies. |
format | Online Article Text |
id | pubmed-4962295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-49622952016-08-08 Horizontal gene transfer: essentiality and evolvability in prokaryotes, and roles in evolutionary transitions Koonin, Eugene V. F1000Res Review The wide spread of gene exchange and loss in the prokaryotic world has prompted the concept of ‘lateral genomics’ to the point of an outright denial of the relevance of phylogenetic trees for evolution. However, the pronounced coherence congruence of the topologies of numerous gene trees, particularly those for (nearly) universal genes, translates into the notion of a statistical tree of life (STOL), which reflects a central trend of vertical evolution. The STOL can be employed as a framework for reconstruction of the evolutionary processes in the prokaryotic world. Quantitatively, however, horizontal gene transfer (HGT) dominates microbial evolution, with the rate of gene gain and loss being comparable to the rate of point mutations and much greater than the duplication rate. Theoretical models of evolution suggest that HGT is essential for the survival of microbial populations that otherwise deteriorate due to the Muller’s ratchet effect. Apparently, at least some bacteria and archaea evolved dedicated vehicles for gene transfer that evolved from selfish elements such as plasmids and viruses. Recent phylogenomic analyses suggest that episodes of massive HGT were pivotal for the emergence of major groups of organisms such as multiple archaeal phyla as well as eukaryotes. Similar analyses appear to indicate that, in addition to donating hundreds of genes to the emerging eukaryotic lineage, mitochondrial endosymbiosis severely curtailed HGT. These results shed new light on the routes of evolutionary transitions, but caution is due given the inherent uncertainty of deep phylogenies. F1000Research 2016-07-25 /pmc/articles/PMC4962295/ /pubmed/27508073 http://dx.doi.org/10.12688/f1000research.8737.1 Text en Copyright: © 2016 Koonin EV http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The author(s) is/are employees of the US Government and therefore domestic copyright protection in USA does not apply to this work. The work may be protected under the copyright laws of other jurisdictions when used in those jurisdictions. |
spellingShingle | Review Koonin, Eugene V. Horizontal gene transfer: essentiality and evolvability in prokaryotes, and roles in evolutionary transitions |
title | Horizontal gene transfer: essentiality and evolvability in prokaryotes, and roles in evolutionary transitions |
title_full | Horizontal gene transfer: essentiality and evolvability in prokaryotes, and roles in evolutionary transitions |
title_fullStr | Horizontal gene transfer: essentiality and evolvability in prokaryotes, and roles in evolutionary transitions |
title_full_unstemmed | Horizontal gene transfer: essentiality and evolvability in prokaryotes, and roles in evolutionary transitions |
title_short | Horizontal gene transfer: essentiality and evolvability in prokaryotes, and roles in evolutionary transitions |
title_sort | horizontal gene transfer: essentiality and evolvability in prokaryotes, and roles in evolutionary transitions |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962295/ https://www.ncbi.nlm.nih.gov/pubmed/27508073 http://dx.doi.org/10.12688/f1000research.8737.1 |
work_keys_str_mv | AT koonineugenev horizontalgenetransferessentialityandevolvabilityinprokaryotesandrolesinevolutionarytransitions |