Jan-Niklas Runge, Kristian Ullrich, Anna K. Lindholm
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Despite that difference, they differ much less from each other than the rest of the chromosome. However, the differences that they have were much more likely to be deleterious than the differences between the two variants of the rest of the chromosome. We interpret this marked difference as evidence of the accumulation of deleterious variants, a hallmark of deterioration. The t region of chromosome 17 is more distant to the reference than the rest of the chromosome, and has a higher fraction of impactful differences here as well. Thus, we conclude that the t appears as a quickly spreading and deteriorating selfish supergene, a rare example of Muller's ratchet outside of sex chromosomes. 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引用次数: 0
摘要
超级基因是由于罕见或不存在重组而共同传播的DNA连接簇。它们进行共同适应,使进化能够在多个基因上发挥作用,完善复杂的表型,从而使超级基因具有竞争优势。然而,由于缺乏重组,超级基因无法有效清除有害 DNA,因此容易退化。除性染色体外,很少有其他例子可供研究。在这里,我们首次组装了家鼠的 t 单倍型,这是一个 33.4 Mb 的超级基因,它以非孟德尔频率 "自私 "地传播自己。我们描述了构成 t 单倍型的四个大的非重叠倒位。我们比较了 t/t 个体中两种不同的 t 变体,它们具有不同的隐性致死表型(死亡年龄)。尽管存在差异,但它们之间的差异比染色体其他部分的差异要小得多。然而,它们之间的差异比染色体其他部分的两个变体之间的差异更有可能造成有害影响。我们将这种明显的差异解释为有害变体积累的证据,这是退化的标志。与其他染色体相比,17 号染色体的 t 区与参照区的距离更远,这里有影响的差异比例也更高。因此,我们得出结论:t 是一个迅速扩散和退化的自私超级基因,是性染色体之外穆勒棘轮现象的一个罕见例子。此外,我们的目标是为 t 单倍型的比较工作(如进化史)提供资源。
De novo assembly of the selfish t supergene reveals a deleterious evolutionary trajectory
Supergenes are linked clusters of DNA that are transmitted together due to rare or absent recombination. They undergo co-adaptation, allowing evolution to work on several genes to refine complex phenotypes, giving supergenes a competitive edge. Yet, due to their lack of recombination, supergenes are susceptible to deterioration as they cannot efficiently purge deleterious DNA. Few examples outside of sex chromosomes have been available for study. Here, we present the first assembly of the t haplotype, a 33.4 Mb supergene in house mice that 'selfishly' transmits itself at non-Mendelian frequencies. We characterize the four large non-overlapping inversions that make up the t haplotype. We compare in a t/t individual two different t variants with different recessive lethal phenotypes (age at death). Despite that difference, they differ much less from each other than the rest of the chromosome. However, the differences that they have were much more likely to be deleterious than the differences between the two variants of the rest of the chromosome. We interpret this marked difference as evidence of the accumulation of deleterious variants, a hallmark of deterioration. The t region of chromosome 17 is more distant to the reference than the rest of the chromosome, and has a higher fraction of impactful differences here as well. Thus, we conclude that the t appears as a quickly spreading and deteriorating selfish supergene, a rare example of Muller's ratchet outside of sex chromosomes. Furthermore, we aim for our assembly to provide a resource for comparative work on the t haplotype, such as its evolutionary history.