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从进化医学角度看尼安德特人的灭绝。

An evolutionary medicine perspective on Neandertal extinction.

作者信息

Sullivan Alexis P, de Manuel Marc, Marques-Bonet Tomas, Perry George H

机构信息

Department of Biology, Pennsylvania State University, University Park, PA 16802, USA.

Institut de Biologia Evolutiva (CSIC/UPF), Parque de Investigación Biomédica de Barcelona (PRBB), Barcelona, Catalonia 08003, Spain.

出版信息

J Hum Evol. 2017 Jul;108:62-71. doi: 10.1016/j.jhevol.2017.03.004. Epub 2017 May 16.

Abstract

The Eurasian sympatry of Neandertals and anatomically modern humans - beginning at least 45,000 years ago and possibly lasting for more than 5000 years - has sparked immense anthropological interest into the factors that potentially contributed to Neandertal extinction. Among many different hypotheses, the "differential pathogen resistance" extinction model posits that Neandertals were disproportionately affected by exposure to novel infectious diseases that were transmitted during the period of spatiotemporal sympatry with modern humans. Comparisons of new archaic hominin paleogenome sequences with modern human genomes have confirmed a history of genetic admixture - and thus direct contact - between humans and Neandertals. Analyses of these data have also shown that Neandertal nuclear genome genetic diversity was likely considerably lower than that of the Eurasian anatomically modern humans with whom they came into contact, perhaps leaving Neandertal innate immune systems relatively more susceptible to novel pathogens. In this study, we compared levels of genetic diversity in genes for which genetic variation is hypothesized to benefit pathogen defense among Neandertals and African, European, and Asian modern humans, using available exome sequencing data (three individuals, or six chromosomes, per population). We observed that Neandertals had only 31-39% as many nonsynonymous (amino acid changing) polymorphisms across 73 innate immune system genes compared to modern human populations. We also found that Neandertal genetic diversity was relatively low in an unbiased set of balancing selection candidate genes for primates, those genes with the highest 1% genetic diversity genome-wide in non-human hominoids (apes). In contrast, Neandertals had similar or higher levels of genetic diversity than humans in 12 major histocompatibility complex (MHC) genes. Thus, while Neandertals may have been relatively more susceptible to some novel pathogens and differential pathogen resistance could be considered as one potential contributing factor in their extinction, the expectations of this model are not universally met.

摘要

尼安德特人与解剖学意义上的现代人类在欧亚大陆的同域分布——至少始于45000年前,可能持续了5000多年——引发了人类学对可能导致尼安德特人灭绝的因素的极大兴趣。在众多不同的假说中,“差异病原体抗性”灭绝模型假定,在与现代人类时空同域分布的时期,尼安德特人因接触新出现的传染病而受到的影响尤为严重。将新的古人类古基因组序列与现代人类基因组进行比较,证实了人类与尼安德特人之间存在基因混合的历史——进而证明了二者有过直接接触。对这些数据的分析还表明,尼安德特人的核基因组遗传多样性可能远低于与之接触的欧亚大陆解剖学意义上的现代人类,这或许使尼安德特人的先天免疫系统相对更容易受到新病原体的影响。在本研究中,我们利用现有的外显子组测序数据(每个群体三个个体,即六条染色体),比较了尼安德特人以及非洲、欧洲和亚洲现代人类中,那些被认为其基因变异有利于病原体防御的基因的遗传多样性水平。我们观察到,与现代人类群体相比,尼安德特人在73个先天免疫系统基因中,非同义(氨基酸改变)多态性的数量仅为现代人类的31%至39%。我们还发现,在一组无偏倚的灵长类平衡选择候选基因中,即那些在非人类灵长类动物(猿类)中全基因组遗传多样性最高的1%的基因,尼安德特人的遗传多样性相对较低。相比之下,尼安德特人在12个主要组织相容性复合体(MHC)基因中的遗传多样性水平与人类相似或更高。因此,虽然尼安德特人可能相对更容易受到某些新病原体的影响,差异病原体抗性可被视为其灭绝的一个潜在因素,但该模型的预期并非完全得到满足。

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