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Testing the retroelement invasion hypothesis for the emergence of the ancestral eukaryotic cell

Phylogenetic evidence suggests that the invasion and proliferation of retroelements, selfish mobile genetic elements that copy and paste themselves within a host genome, was one of the early evolutionary events in the emergence of eukaryotes. Here we test the effects of this event by determining the...

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Autores principales: Lee, Gloria, Sherer, Nicholas A., Kim, Neil H., Rajic, Ema, Kaur, Davneet, Urriola, Niko, Martini, K. Michael, Xue, Chi, Goldenfeld, Nigel, Kuhlman, Thomas E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6298092/
https://www.ncbi.nlm.nih.gov/pubmed/30455297
http://dx.doi.org/10.1073/pnas.1807709115
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author Lee, Gloria
Sherer, Nicholas A.
Kim, Neil H.
Rajic, Ema
Kaur, Davneet
Urriola, Niko
Martini, K. Michael
Xue, Chi
Goldenfeld, Nigel
Kuhlman, Thomas E.
author_facet Lee, Gloria
Sherer, Nicholas A.
Kim, Neil H.
Rajic, Ema
Kaur, Davneet
Urriola, Niko
Martini, K. Michael
Xue, Chi
Goldenfeld, Nigel
Kuhlman, Thomas E.
author_sort Lee, Gloria
collection PubMed
description Phylogenetic evidence suggests that the invasion and proliferation of retroelements, selfish mobile genetic elements that copy and paste themselves within a host genome, was one of the early evolutionary events in the emergence of eukaryotes. Here we test the effects of this event by determining the pressures retroelements exert on simple genomes. We transferred two retroelements, human LINE-1 and the bacterial group II intron Ll.LtrB, into bacteria, and find that both are functional and detrimental to growth. We find, surprisingly, that retroelement lethality and proliferation are enhanced by the ability to perform eukaryotic-like nonhomologous end-joining (NHEJ) DNA repair. We show that the only stable evolutionary consequence in simple cells is maintenance of retroelements in low numbers, suggesting how retrotransposition rates and costs in early eukaryotes could have been constrained to allow proliferation. Our results suggest that the interplay between NHEJ and retroelements may have played a fundamental and previously unappreciated role in facilitating the proliferation of retroelements, elements of which became the ancestors of the spliceosome components in eukaryotes.
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spelling pubmed-62980922018-12-21 Testing the retroelement invasion hypothesis for the emergence of the ancestral eukaryotic cell Lee, Gloria Sherer, Nicholas A. Kim, Neil H. Rajic, Ema Kaur, Davneet Urriola, Niko Martini, K. Michael Xue, Chi Goldenfeld, Nigel Kuhlman, Thomas E. Proc Natl Acad Sci U S A Biological Sciences Phylogenetic evidence suggests that the invasion and proliferation of retroelements, selfish mobile genetic elements that copy and paste themselves within a host genome, was one of the early evolutionary events in the emergence of eukaryotes. Here we test the effects of this event by determining the pressures retroelements exert on simple genomes. We transferred two retroelements, human LINE-1 and the bacterial group II intron Ll.LtrB, into bacteria, and find that both are functional and detrimental to growth. We find, surprisingly, that retroelement lethality and proliferation are enhanced by the ability to perform eukaryotic-like nonhomologous end-joining (NHEJ) DNA repair. We show that the only stable evolutionary consequence in simple cells is maintenance of retroelements in low numbers, suggesting how retrotransposition rates and costs in early eukaryotes could have been constrained to allow proliferation. Our results suggest that the interplay between NHEJ and retroelements may have played a fundamental and previously unappreciated role in facilitating the proliferation of retroelements, elements of which became the ancestors of the spliceosome components in eukaryotes. National Academy of Sciences 2018-12-04 2018-11-19 /pmc/articles/PMC6298092/ /pubmed/30455297 http://dx.doi.org/10.1073/pnas.1807709115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Lee, Gloria
Sherer, Nicholas A.
Kim, Neil H.
Rajic, Ema
Kaur, Davneet
Urriola, Niko
Martini, K. Michael
Xue, Chi
Goldenfeld, Nigel
Kuhlman, Thomas E.
Testing the retroelement invasion hypothesis for the emergence of the ancestral eukaryotic cell
title Testing the retroelement invasion hypothesis for the emergence of the ancestral eukaryotic cell
title_full Testing the retroelement invasion hypothesis for the emergence of the ancestral eukaryotic cell
title_fullStr Testing the retroelement invasion hypothesis for the emergence of the ancestral eukaryotic cell
title_full_unstemmed Testing the retroelement invasion hypothesis for the emergence of the ancestral eukaryotic cell
title_short Testing the retroelement invasion hypothesis for the emergence of the ancestral eukaryotic cell
title_sort testing the retroelement invasion hypothesis for the emergence of the ancestral eukaryotic cell
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6298092/
https://www.ncbi.nlm.nih.gov/pubmed/30455297
http://dx.doi.org/10.1073/pnas.1807709115
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