Accelerated adaptive evolution on a newly formed X chromosome.

Sex chromosomes originated from ordinary autosomes, and their evolution is characterized by continuous gene loss from the ancestral Y chromosome. Here, we document a new feature of sex chromosome evolution: bursts of adaptive fixations on a newly formed X chromosome. Taking advantage of the recently...

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Autores principales: Doris Bachtrog, Jeffrey D Jensen, Zhi Zhang
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Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2009
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spelling oai:doaj.org-article:95385474ddad4a10885043c2978d32892021-11-25T05:34:13ZAccelerated adaptive evolution on a newly formed X chromosome.1544-91731545-788510.1371/journal.pbio.1000082https://doaj.org/article/95385474ddad4a10885043c2978d32892009-04-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19402745/?tool=EBIhttps://doaj.org/toc/1544-9173https://doaj.org/toc/1545-7885Sex chromosomes originated from ordinary autosomes, and their evolution is characterized by continuous gene loss from the ancestral Y chromosome. Here, we document a new feature of sex chromosome evolution: bursts of adaptive fixations on a newly formed X chromosome. Taking advantage of the recently formed neo-X chromosome of Drosophila miranda, we compare patterns of DNA sequence variation at genes located on the neo-X to genes on the ancestral X chromosome. This contrast allows us to draw inferences of selection on a newly formed X chromosome relative to background levels of adaptation in the genome while controlling for demographic effects. Chromosome-wide synonymous diversity on the neo-X is reduced 2-fold relative to the ancestral X, as expected under recent and recurrent directional selection. Several statistical tests employing various features of the data consistently identify 10%-15% of neo-X genes as targets of recent adaptive evolution but only 1%-3% of genes on the ancestral X. In addition, both the rate of adaptation and the fitness effects of adaptive substitutions are estimated to be roughly an order of magnitude higher for neo-X genes relative to genes on the ancestral X. Thus, newly formed X chromosomes are not passive players in the evolutionary process of sex chromosome differentiation, but respond adaptively to both their sex-biased transmission and to Y chromosome degeneration, possibly through demasculinization of their gene content and the evolution of dosage compensation.Doris BachtrogJeffrey D JensenZhi ZhangPublic Library of Science (PLoS)articleBiology (General)QH301-705.5ENPLoS Biology, Vol 7, Iss 4, p e82 (2009)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Doris Bachtrog
Jeffrey D Jensen
Zhi Zhang
Accelerated adaptive evolution on a newly formed X chromosome.
description Sex chromosomes originated from ordinary autosomes, and their evolution is characterized by continuous gene loss from the ancestral Y chromosome. Here, we document a new feature of sex chromosome evolution: bursts of adaptive fixations on a newly formed X chromosome. Taking advantage of the recently formed neo-X chromosome of Drosophila miranda, we compare patterns of DNA sequence variation at genes located on the neo-X to genes on the ancestral X chromosome. This contrast allows us to draw inferences of selection on a newly formed X chromosome relative to background levels of adaptation in the genome while controlling for demographic effects. Chromosome-wide synonymous diversity on the neo-X is reduced 2-fold relative to the ancestral X, as expected under recent and recurrent directional selection. Several statistical tests employing various features of the data consistently identify 10%-15% of neo-X genes as targets of recent adaptive evolution but only 1%-3% of genes on the ancestral X. In addition, both the rate of adaptation and the fitness effects of adaptive substitutions are estimated to be roughly an order of magnitude higher for neo-X genes relative to genes on the ancestral X. Thus, newly formed X chromosomes are not passive players in the evolutionary process of sex chromosome differentiation, but respond adaptively to both their sex-biased transmission and to Y chromosome degeneration, possibly through demasculinization of their gene content and the evolution of dosage compensation.
format article
author Doris Bachtrog
Jeffrey D Jensen
Zhi Zhang
author_facet Doris Bachtrog
Jeffrey D Jensen
Zhi Zhang
author_sort Doris Bachtrog
title Accelerated adaptive evolution on a newly formed X chromosome.
title_short Accelerated adaptive evolution on a newly formed X chromosome.
title_full Accelerated adaptive evolution on a newly formed X chromosome.
title_fullStr Accelerated adaptive evolution on a newly formed X chromosome.
title_full_unstemmed Accelerated adaptive evolution on a newly formed X chromosome.
title_sort accelerated adaptive evolution on a newly formed x chromosome.
publisher Public Library of Science (PLoS)
publishDate 2009
url https://doaj.org/article/95385474ddad4a10885043c2978d3289
work_keys_str_mv AT dorisbachtrog acceleratedadaptiveevolutiononanewlyformedxchromosome
AT jeffreydjensen acceleratedadaptiveevolutiononanewlyformedxchromosome
AT zhizhang acceleratedadaptiveevolutiononanewlyformedxchromosome
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