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Deeply conserved synteny resolves early events in vertebrate evolution

Although it is widely believed that early vertebrate evolution was shaped by ancient whole-genome duplications, the number, timing and mechanism of these events remain elusive. Here, we infer the history of vertebrates through genomic comparisons with a new chromosome-scale sequence of the invertebr...

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Autores principales: Simakov, Oleg, Marlétaz, Ferdinand, Yue, Jia-Xing, O’Connell, Brendan, Jenkins, Jerry, Brandt, Alexander, Calef, Robert, Tung, Che-Huang, Huang, Tzu-Kai, Schmutz, Jeremy, Satoh, Nori, Yu, Jr-Kai, Putnam, Nicholas H., Green, Richard E., Rokhsar, Daniel S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7269912/
https://www.ncbi.nlm.nih.gov/pubmed/32313176
http://dx.doi.org/10.1038/s41559-020-1156-z
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author Simakov, Oleg
Marlétaz, Ferdinand
Yue, Jia-Xing
O’Connell, Brendan
Jenkins, Jerry
Brandt, Alexander
Calef, Robert
Tung, Che-Huang
Huang, Tzu-Kai
Schmutz, Jeremy
Satoh, Nori
Yu, Jr-Kai
Putnam, Nicholas H.
Green, Richard E.
Rokhsar, Daniel S.
author_facet Simakov, Oleg
Marlétaz, Ferdinand
Yue, Jia-Xing
O’Connell, Brendan
Jenkins, Jerry
Brandt, Alexander
Calef, Robert
Tung, Che-Huang
Huang, Tzu-Kai
Schmutz, Jeremy
Satoh, Nori
Yu, Jr-Kai
Putnam, Nicholas H.
Green, Richard E.
Rokhsar, Daniel S.
author_sort Simakov, Oleg
collection PubMed
description Although it is widely believed that early vertebrate evolution was shaped by ancient whole-genome duplications, the number, timing and mechanism of these events remain elusive. Here, we infer the history of vertebrates through genomic comparisons with a new chromosome-scale sequence of the invertebrate chordate amphioxus. We show how the karyotypes of amphioxus and diverse vertebrates are derived from 17 ancestral chordate linkage groups (and 19 ancestral bilaterian groups) by fusion, rearrangement and duplication. We resolve two distinct ancient duplications based on patterns of chromosomal conserved synteny. All extant vertebrates share the first duplication, which occurred in the mid/late Cambrian by autotetraploidization (that is, direct genome doubling). In contrast, the second duplication is found only in jawed vertebrates and occurred in the mid–late Ordovician by allotetraploidization (that is, genome duplication following interspecific hybridization) from two now-extinct progenitors. This complex genomic history parallels the diversification of vertebrate lineages in the fossil record.
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spelling pubmed-72699122020-06-15 Deeply conserved synteny resolves early events in vertebrate evolution Simakov, Oleg Marlétaz, Ferdinand Yue, Jia-Xing O’Connell, Brendan Jenkins, Jerry Brandt, Alexander Calef, Robert Tung, Che-Huang Huang, Tzu-Kai Schmutz, Jeremy Satoh, Nori Yu, Jr-Kai Putnam, Nicholas H. Green, Richard E. Rokhsar, Daniel S. Nat Ecol Evol Article Although it is widely believed that early vertebrate evolution was shaped by ancient whole-genome duplications, the number, timing and mechanism of these events remain elusive. Here, we infer the history of vertebrates through genomic comparisons with a new chromosome-scale sequence of the invertebrate chordate amphioxus. We show how the karyotypes of amphioxus and diverse vertebrates are derived from 17 ancestral chordate linkage groups (and 19 ancestral bilaterian groups) by fusion, rearrangement and duplication. We resolve two distinct ancient duplications based on patterns of chromosomal conserved synteny. All extant vertebrates share the first duplication, which occurred in the mid/late Cambrian by autotetraploidization (that is, direct genome doubling). In contrast, the second duplication is found only in jawed vertebrates and occurred in the mid–late Ordovician by allotetraploidization (that is, genome duplication following interspecific hybridization) from two now-extinct progenitors. This complex genomic history parallels the diversification of vertebrate lineages in the fossil record. Nature Publishing Group UK 2020-04-20 2020 /pmc/articles/PMC7269912/ /pubmed/32313176 http://dx.doi.org/10.1038/s41559-020-1156-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Simakov, Oleg
Marlétaz, Ferdinand
Yue, Jia-Xing
O’Connell, Brendan
Jenkins, Jerry
Brandt, Alexander
Calef, Robert
Tung, Che-Huang
Huang, Tzu-Kai
Schmutz, Jeremy
Satoh, Nori
Yu, Jr-Kai
Putnam, Nicholas H.
Green, Richard E.
Rokhsar, Daniel S.
Deeply conserved synteny resolves early events in vertebrate evolution
title Deeply conserved synteny resolves early events in vertebrate evolution
title_full Deeply conserved synteny resolves early events in vertebrate evolution
title_fullStr Deeply conserved synteny resolves early events in vertebrate evolution
title_full_unstemmed Deeply conserved synteny resolves early events in vertebrate evolution
title_short Deeply conserved synteny resolves early events in vertebrate evolution
title_sort deeply conserved synteny resolves early events in vertebrate evolution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7269912/
https://www.ncbi.nlm.nih.gov/pubmed/32313176
http://dx.doi.org/10.1038/s41559-020-1156-z
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