Suppr超能文献

部分隐性有害遗传变异对抑制性染色体间重组倒位进化的影响 1 。

Consequences of partially recessive deleterious genetic variation for the evolution of inversions suppressing recombination between sex chromosomes1.

机构信息

Department of Biology, Lund University, Lund, Sweden.

出版信息

Evolution. 2024 Jul 29;78(8):1499-1510. doi: 10.1093/evolut/qpae060.

Abstract

The evolution of suppressed recombination between sex chromosomes is widely hypothesized to be driven by sexually antagonistic selection (SA), where tighter linkage between the sex-determining gene(s) and nearby SA loci is favored when it couples male-beneficial alleles to the proto-Y chromosome, and female-beneficial alleles to the proto-X. Although difficult to test empirically, the SA selection hypothesis overshadows several alternatives, including an incomplete but often-repeated "sheltering" hypothesis which suggests that expansion of the sex-linked region (SLR) reduces the homozygous expression of deleterious mutations at selected loci. Here, we use population genetic models to evaluate the consequences of partially recessive deleterious mutational variation for the evolution of otherwise neutral chromosomal inversions expanding the SLR on proto-Y chromosomes. Both autosomal and SLR-expanding inversions face a race against time: lightly-loaded inversions are initially beneficial, but eventually become deleterious as they accumulate new mutations, after which their chances of fixing become negligible. In contrast, initially unloaded inversions eventually become neutral as their deleterious load reaches the same equilibrium as non-inverted haplotypes. Despite the differences in inheritance and indirect selection, SLR-expanding inversions exhibit similar evolutionary dynamics to autosomal inversions over many biologically plausible parameter conditions. Differences emerge when the population average mutation load is quite high; in this case large autosomal inversions that are lucky enough to be mutation-free can rise to intermediate to high frequencies where selection in homozygotes becomes important (Y-linked inversions never appear as homozygous karyotypes); conditions requiring either high mutation rates, highly recessive deleterious mutations, weak selection, or a combination thereof.

摘要

性染色体间重组抑制的进化被广泛假设为受到性拮抗选择(SA)的驱动,即当与雄性有利等位基因相连的性决定基因(s)和附近的 SA 基因座与原 Y 染色体紧密连锁,而与雌性有利等位基因相连的则与原 X 染色体紧密连锁时,这种连锁更受青睐。尽管很难从经验上进行检验,但 SA 选择假说掩盖了几个替代假说,包括一个不完整但经常被重复的“庇护”假说,该假说表明,性连锁区(SLR)的扩张减少了选择位点上有害突变的纯合表达。在这里,我们使用群体遗传模型来评估部分隐性有害突变变异对 otherwise neutral chromosomal inversions 的进化的影响,这些 inversion 扩展了原 Y 染色体上的 SLR。常染色体和 SLR 扩展的倒位都面临着与时间的赛跑:负载较轻的倒位最初是有利的,但随着它们积累新的突变,最终会变得有害,此后它们固定的机会变得微不足道。相比之下,最初未加载的倒位最终会变得中性,因为它们的有害负荷与非倒位单倍型达到相同的平衡。尽管在遗传和间接选择上存在差异,但在许多合理的生物学参数条件下,SLR 扩展的倒位与常染色体倒位表现出相似的进化动态。当种群平均突变负荷相当高时,就会出现差异;在这种情况下,足够幸运的没有突变的大常染色体倒位可以上升到中等至高频率,此时纯合子中的选择变得重要(Y 染色体倒位永远不会出现纯合核型);需要高突变率、高度隐性有害突变、弱选择或它们的组合的条件。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验