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Reconciling theories of dominance with the relative rates of adaptive substitution on sex chromosomes and autosomes.协调主导理论与性染色体和常染色体上适应性替代的相对速率。
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本文引用的文献

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The evolution of genetic covariance and modularity as a result of multigenerational environmental fluctuation.多代环境波动导致的遗传协方差和模块性的演变。
Evol Lett. 2023 Oct 17;7(6):457-466. doi: 10.1093/evlett/qrad048. eCollection 2023 Dec.
2
Why is measuring and predicting fitness under genomic conflict so hard?为什么在基因组冲突下测量和预测适应性如此困难?
Curr Opin Genet Dev. 2023 Aug;81:102070. doi: 10.1016/j.gde.2023.102070. Epub 2023 Jun 25.
3
Amplification is the primary mode of gene-by-sex interaction in complex human traits.在复杂的人类性状中,基因与性别的相互作用主要模式是基因扩增。
Cell Genom. 2023 Apr 6;3(5):100297. doi: 10.1016/j.xgen.2023.100297. eCollection 2023 May 10.
4
Recombination and selection against introgressed DNA.针对渗入DNA的重组与选择
Evolution. 2023 Apr 1;77(4):1131-1144. doi: 10.1093/evolut/qpad021.
5
Genetic sex determination, sex chromosome size and sex-specific lifespans across tetrapods.四足动物的遗传性别决定、性染色体大小和性别特异性寿命。
J Evol Biol. 2023 Feb;36(2):480-494. doi: 10.1111/jeb.14130. Epub 2022 Dec 20.
6
Rapid evolution of ecological sexual dimorphism driven by resource competition.资源竞争驱动生态性别二态性的快速进化。
Ecol Lett. 2023 Jan;26(1):124-131. doi: 10.1111/ele.14140. Epub 2022 Nov 10.
7
Polygenic adaptation after a sudden change in environment.环境骤变后的多基因适应。
Elife. 2022 Sep 26;11:e66697. doi: 10.7554/eLife.66697.
8
How much does the unguarded X contribute to sex differences in life span?未受保护的X因素对寿命的性别差异有多大影响?
Evol Lett. 2022 Jul 5;6(4):319-329. doi: 10.1002/evl3.292. eCollection 2022 Aug.
9
Y recombination arrest and degeneration in the absence of sexual dimorphism.Y 重组抑制与性二态性缺失导致的退化。
Science. 2022 Feb 11;375(6581):663-666. doi: 10.1126/science.abj1813. Epub 2022 Feb 10.
10
An unbiased test reveals no enrichment of sexually antagonistic polymorphisms on the human X chromosome.一项无偏测试并未揭示人类 X 染色体上性拮抗多态性的富集。
Proc Biol Sci. 2022 Jan 26;289(1967):20212314. doi: 10.1098/rspb.2021.2314.

性染色体对性拮抗的多基因反应。

Polygenic response of sex chromosomes to sexual antagonism.

作者信息

Muralidhar Pavitra, Coop Graham

机构信息

Center for Population Biology, University of California, Davis, CA, United States.

Department of Evolution and Ecology, University of California, Davis, CA, United States.

出版信息

Evolution. 2024 Feb 29;78(3):539-554. doi: 10.1093/evolut/qpad231.

DOI:10.1093/evolut/qpad231
PMID:38153370
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10903542/
Abstract

Sexual antagonism occurs when males and females differ in their phenotypic fitness optima but are constrained in their evolution to these optima because of their shared genome. The sex chromosomes, which have distinct evolutionary "interests" relative to the autosomes, are theorized to play an important role in sexually antagonistic conflict. However, the evolutionary responses of sex chromosomes and autosomes have usually been considered independently, that is, via contrasting the response of a gene located on either an X chromosome or an autosome. Here, we study the coevolutionary response of the X chromosome and autosomes to sexually antagonistic selection acting on a polygenic phenotype. We model a phenotype initially under stabilizing selection around a single optimum, followed by a sudden divergence of the male and female optima. We find that, in the absence of dosage compensation, the X chromosome promotes evolution toward the female optimum, inducing coevolutionary male-biased responses on the autosomes. Dosage compensation obscures the female-biased interests of the X, causing it to contribute equally to male and female phenotypic change. We further demonstrate that fluctuations in an adaptive landscape can generate prolonged intragenomic conflict and accentuate the differential responses of the X and autosomes to this conflict.

摘要

当雄性和雌性在表型适合度最优值上存在差异,但由于共享基因组而在进化上受到这些最优值的限制时,就会出现性拮抗。相对于常染色体,性染色体具有独特的进化“利益”,理论上在性拮抗冲突中发挥重要作用。然而,性染色体和常染色体的进化反应通常被独立考虑,即通过对比位于X染色体或常染色体上的基因的反应。在这里,我们研究了X染色体和常染色体对作用于多基因表型的性拮抗选择的共同进化反应。我们构建了一个模型,该模型中的表型最初在围绕单一最优值的稳定选择下,随后雄性和雌性最优值突然出现分歧。我们发现,在没有剂量补偿的情况下,X染色体促进向雌性最优值的进化,在常染色体上诱导共同进化的雄性偏向反应。剂量补偿掩盖了X染色体偏向雌性的利益,使其对雄性和雌性表型变化的贡献相等。我们进一步证明,适应性景观的波动会产生长期的基因组内冲突,并加剧X染色体和常染色体对这种冲突的不同反应。