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Evolution of a malaria resistance gene in wild primates

机译:野生灵长类动物疟疾抗性基因的进化

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摘要

The ecology, behaviour and genetics of our closest living relatives, the nonhuman primates, should help us to understand the evolution of our own lineage. Although a large amount of data has been amassed on primate ecology and behaviour, much less is known about the functional and evolutionary genetic aspects of primate biology, especially in wild primates. As a result, even in well-studied populations in which nongenetic factors that influence adaptively important characteristics have been identified, we have almost no understanding of the underlying genetic basis for such traits. Here, we report on the functional consequences of genetic variation at the malaria-related FY (DARC) gene in a well-studied population of yellow baboons (Papio cynocephalus) living in Amboseli National Park in Kenya. FYcodes for a chemokine receptor normally expressed on the erythrocyte surface that is the known entry point for the malarial parasite Plasmodium vivax. We identified variation in the cis-regulatory region of the baboon FY gene that was associated with phenotypic variation in susceptibility to Hepatocystis, a malaria-like pathogen that is common in baboons. Genetic variation in this region also influenced gene expression in vivo in wild individuals, a result we confirmed using in vitro reporter gene assays. The patterns of genetic variation in and around this locus were also suggestive of non-neutral evolution, raising the possibility that the evolution of the FY cis-regulatory region in baboons has exhibited both mechanistic and selective parallels with the homologous region in humans. Together, our results represent the first reported association and functional characterization Unking genetic variation and a complex trait in a natural population of nonhuman primates.
机译:我们最亲近的亲戚(非人类灵长类动物)的生态,行为和遗传学应该有助于我们了解自己血统的演变。尽管已经积累了有关灵长类动物生态学和行为的大量数据,但是人们对灵长类动物生物学的功能和进化遗传方面的了解还很少,尤其是在野生灵长类动物中。结果,即使在研究充分的人群中,已经确定出影响自适应重要特征的非遗传因素,我们也几乎不了解此类特征的潜在遗传基础。在这里,我们报告了居住在肯尼亚安博塞利国家公园的经过充分研究的黄色狒狒(Papio cynocephalus)种群中与疟疾相关的FY(DARC)基因遗传变异的功能后果。通常在红细胞表面上表达的趋化因子受体的FY代码,这是疟原虫间日疟原虫的已知入口点。我们确定了狒狒FY基因的顺式调节区域中的变异与对肝囊肿(一种在狒狒中常见的疟疾样病原体)的易感性的表型变异有关。该区域的遗传变异也影响了野生个体体内的基因表达,我们使用体外报道基因测定证实了这一结果。该基因座及其周围的遗传变异模式也暗示了非中性进化,这增加了狒狒FY顺式调控区的进化与人类同源区在机制上和选择性上都相似的可能性。总之,我们的结果代表了首次报道的非人类灵长类自然种群中Unking基因变异和复杂性状的关联和功能表征。

著录项

  • 来源
    《Nature》 |2009年第7253期|388-391qt03|共5页
  • 作者单位

    Department of Biology, Duke University Institute for Genome Sciences and Policy, Duke University;

    Department of Biology, Duke University Institute for Genome Sciences and Policy, Duke University;

    Department of Biology, Duke University;

    Institute for Genome Sciences and Policy, Duke University;

    Department of Biology, Duke University Institute for Genome Sciences and Policy, Duke University Department of Evolutionary Anthropology, Duke University, Durham, North Carolina 27708, USA Institute of Primate Research, National Museums of Kenya, Nairobi, Kenya;

    Department of Biology, Duke University Institute for Genome Sciences and Policy, Duke University Department of Evolutionary Anthropology, Duke University, Durham, North Carolina 27708, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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