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Extinction of chromosomes due to specialization is a universal occurrence

The human X and Y chromosomes evolved from a pair of autosomes approximately 180 million years ago. Despite their shared evolutionary origin, extensive genetic decay has resulted in the human Y chromosome losing 97% of its ancestral genes while gene content and order remain highly conserved on the X...

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Autores principales: Wilson, Jason, Staley, Joshua M., Wyckoff, Gerald J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005762/
https://www.ncbi.nlm.nih.gov/pubmed/32034231
http://dx.doi.org/10.1038/s41598-020-58997-2
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author Wilson, Jason
Staley, Joshua M.
Wyckoff, Gerald J.
author_facet Wilson, Jason
Staley, Joshua M.
Wyckoff, Gerald J.
author_sort Wilson, Jason
collection PubMed
description The human X and Y chromosomes evolved from a pair of autosomes approximately 180 million years ago. Despite their shared evolutionary origin, extensive genetic decay has resulted in the human Y chromosome losing 97% of its ancestral genes while gene content and order remain highly conserved on the X chromosome. Five ‘stratification’ events, most likely inversions, reduced the Y chromosome’s ability to recombine with the X chromosome across the majority of its length and subjected its genes to the erosive forces associated with reduced recombination. The remaining functional genes are ubiquitously expressed, functionally coherent, dosage-sensitive genes, or have evolved male-specific functionality. It is unknown, however, whether functional specialization is a degenerative phenomenon unique to sex chromosomes, or if it conveys a potential selective advantage aside from sexual antagonism. We examined the evolution of mammalian orthologs to determine if the selective forces that led to the degeneration of the Y chromosome are unique in the genome. The results of our study suggest these forces are not exclusive to the Y chromosome, and chromosomal degeneration may have occurred throughout our evolutionary history. The reduction of recombination could additionally result in rapid fixation through isolation of specialized functions resulting in a cost-benefit relationship during times of intense selective pressure.
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spelling pubmed-70057622020-02-18 Extinction of chromosomes due to specialization is a universal occurrence Wilson, Jason Staley, Joshua M. Wyckoff, Gerald J. Sci Rep Article The human X and Y chromosomes evolved from a pair of autosomes approximately 180 million years ago. Despite their shared evolutionary origin, extensive genetic decay has resulted in the human Y chromosome losing 97% of its ancestral genes while gene content and order remain highly conserved on the X chromosome. Five ‘stratification’ events, most likely inversions, reduced the Y chromosome’s ability to recombine with the X chromosome across the majority of its length and subjected its genes to the erosive forces associated with reduced recombination. The remaining functional genes are ubiquitously expressed, functionally coherent, dosage-sensitive genes, or have evolved male-specific functionality. It is unknown, however, whether functional specialization is a degenerative phenomenon unique to sex chromosomes, or if it conveys a potential selective advantage aside from sexual antagonism. We examined the evolution of mammalian orthologs to determine if the selective forces that led to the degeneration of the Y chromosome are unique in the genome. The results of our study suggest these forces are not exclusive to the Y chromosome, and chromosomal degeneration may have occurred throughout our evolutionary history. The reduction of recombination could additionally result in rapid fixation through isolation of specialized functions resulting in a cost-benefit relationship during times of intense selective pressure. Nature Publishing Group UK 2020-02-07 /pmc/articles/PMC7005762/ /pubmed/32034231 http://dx.doi.org/10.1038/s41598-020-58997-2 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
Wilson, Jason
Staley, Joshua M.
Wyckoff, Gerald J.
Extinction of chromosomes due to specialization is a universal occurrence
title Extinction of chromosomes due to specialization is a universal occurrence
title_full Extinction of chromosomes due to specialization is a universal occurrence
title_fullStr Extinction of chromosomes due to specialization is a universal occurrence
title_full_unstemmed Extinction of chromosomes due to specialization is a universal occurrence
title_short Extinction of chromosomes due to specialization is a universal occurrence
title_sort extinction of chromosomes due to specialization is a universal occurrence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005762/
https://www.ncbi.nlm.nih.gov/pubmed/32034231
http://dx.doi.org/10.1038/s41598-020-58997-2
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