探索现代人类昼夜节律基因的适应性导入

Christopher Kendall, Amin Nooranikhojasteh, Guilherme Debortoli, Vinicius Cauê Furlan Roberto, Marla Mendes, David Samson, Esteban Parra, Bence Viola, Michael Schillaci
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引用次数: 0

摘要

随着现代人向非洲以外地区迁移,现代人与古人类(包括尼安德特人和丹尼索瓦人)之间发生了杂交。在这里,我们利用 "人类基因组多样性项目"(Human Genome Diversity Project)和 "1000 基因组项目"(1000 Genomes Project)中的 76 个全球现代人种群,报告了在与昼夜节律和时间型相关的基因组区域内,古人类基因的引入证据。我们计算了常染色体上表明适应性引入的区域的范围,并确定了被认为处于正向选择的区域。我们检测了 36 个核心单倍型中的纬度克隆证据,并提出了每个单倍型可能的古老供体。我们发现了 265 个独立的片段,这些片段与被描述为具有昼夜节律成分的基因重叠,或含有变体,以及先前被确定为与昼夜节律或时间型相关的片段。在这些片段中,我们发现了 1729 个等位基因频率至少为 40% 的古老衍生变体,它们与 303 个基因和基因间片段相交。这些片段中有 17 个显示了正选择的证据,其中 3 个在我们的核心单倍型中发现。我们发现,许多基因与免疫系统或胃肠功能有关。此外,与精神分裂症和双相情感障碍等复杂性状相关的变异也出现在我们的适应性引入区域中。最后,在我们的适应性导入结果中还发现了与睡眠和时间型表型以及血清素通路相关的基因和标记,这可能表明现代人类在离开非洲后迁移到新的环境中时,对与季节性光照变化相关的基因进行了选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring adaptive introgression in modern human circadian rhythm genes
Interbreeding between modern humans and archaic hominins, including Neanderthals and Denisovans, occurred as modern humans migrated outside of Africa. Here, we report on evidence of introgression from archaic hominins within genomic regions associated with circadian rhythm and chronotype using 76 worldwide modern human populations from the Human Genome Diversity Project and 1000 Genomes Project. We calculated the extent of regions indicative of adaptive introgression across the autosomes and identified regions that are suggested to be under positive selection. We tested for evidence of a latitudinal cline within 36 core haplotypes along with presenting the likely archaic donor for each of these haplotypes. We identified 265 independent segments that overlap genes described as having a circadian rhythm component or contain variants and segments previously identified as being associated with circadian rhythm or chronotype. Within these segments we found 1,729 archaically derived variants with allele frequencies of at least 40% intersecting 303 genes and intergenic segments. Seventeen of these segments show evidence of positive selection, three of which are found within our core haplotypes. We found that many of our genes are associated with the immune system or gastrointestinal function. Additionally, variants associated with complex traits such as schizophrenia and bipolar disorder are present within our adaptively introgressed regions. Lastly, genes and markers associated with sleep and chronotype phenotypes and serotonin pathways were also found in our adaptive introgression results, potentially signalling selection on genes related to seasonal light variation as modern humans migrated into new environments after leaving Africa.
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