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

IF 3.1 2区 环境科学与生态学 Q2 ECOLOGY
Evolution Pub Date : 2024-07-29 DOI:10.1093/evolut/qpae060
Colin Olito, Suvi Ponnikas, Bengt Hansson, Jessica K Abbott
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引用次数: 0

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.

部分隐性有害遗传变异对抑制性染色体间重组的倒位进化的影响1。
性染色体之间重组受抑制的进化被广泛认为是由性拮抗选择(SA)驱动的,当性决定基因与附近的SA基因位点之间的连接更紧密时,有利于将对雄性有益的等位基因连接到原Y染色体上,而将对雌性有益的等位基因连接到原X染色体上。尽管难以进行经验检验,但SA选择假说掩盖了几种替代方案,包括一种不完整但经常被重复的 "庇护 "假说,该假说认为性连锁区域(SLR)的扩展减少了所选位点上有害突变的同源表达。在这里,我们利用群体遗传模型来评估部分隐性有害突变变异对原生 Y 染色体上扩大 SLR 的中性染色体倒位进化的影响。常染色体倒位和SLR扩展倒位都面临着与时间的赛跑:轻载倒位最初是有益的,但随着新突变的积累,最终会变成有害的,之后其固定的机会变得微乎其微。与此相反,最初没有负载的倒位最终会变成中性,因为它们的有害负载达到了与非倒位单倍型相同的平衡。尽管在遗传和间接选择方面存在差异,但在许多生物学上可行的参数条件下,SLR扩展倒位与常染色体倒位表现出相似的进化动态。当群体平均突变负荷相当高时,差异就会出现;在这种情况下,幸运地没有突变的大型常染色体倒位现象会上升到中高频率,在这种情况下,对同源染色体的选择变得非常重要(Y 连锁倒位现象从未以同源染色体核型的形式出现);这些条件需要高突变率、高隐性有害突变、弱选择或上述条件的组合。
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来源期刊
Evolution
Evolution 环境科学-进化生物学
CiteScore
5.00
自引率
9.10%
发文量
0
审稿时长
3-6 weeks
期刊介绍: Evolution, published for the Society for the Study of Evolution, is the premier publication devoted to the study of organic evolution and the integration of the various fields of science concerned with evolution. The journal presents significant and original results that extend our understanding of evolutionary phenomena and processes.
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