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人类功能性嗅觉库中的种群差异。

Population differences in the human functional olfactory repertoire.

作者信息

Gilad Yoav, Lancet Doron

机构信息

Department of Molecular Genetics and the Crown Human Genome Center, The Weizmann Institute of Science, Rehovot, Israel.

出版信息

Mol Biol Evol. 2003 Mar;20(3):307-14. doi: 10.1093/molbev/msg013.

Abstract

Olfactory receptors (OR) constitute the molecular basis for the sense of smell. They are encoded by a large multigene family that in humans includes approximately 400 functional genes and approximately 600 putative pseudogenes, distributed on all but two chromosomes. To examine the ethnogeographic variability in the functional chemosensory repertoire, we resequenced 32 OR loci reported to contain a single coding region disruption in seven Caucasians and seven Pygmies. Thirteen of the 32 OR loci were found to have an interrupted coding region in all 28 alleles sampled, seven had an intact form in all the individuals examined, and 12 were polymorphic, segregating both the intact and the null variants. Among the latter loci, the frequency of the null allele was higher in Caucasians than in Pygmies, suggesting that African populations may have a larger repertoire of functional OR genes. Interestingly, when analyzing the entire OR coding regions, we find an excess of high-frequency derived alleles at many loci in the Caucasian sample but less so in the Pygmy sample. Our observations are unlikely to be accounted for by simple demographic models but may be explained by positive selection acting on OR loci in Caucasians.

摘要

嗅觉受体(OR)构成了嗅觉的分子基础。它们由一个庞大的多基因家族编码,在人类中,该家族包括约400个功能基因和约600个假定的假基因,分布于除两条染色体外的所有染色体上。为了研究功能性化学感应库中的种族地理变异性,我们对32个据报道含有单个编码区中断的OR基因座进行了重测序,这些基因座来自7名高加索人和7名俾格米人。在32个OR基因座中,发现13个在所有28个采样等位基因中都有中断的编码区,7个在所有检测个体中都具有完整形式,12个是多态性的,同时分离完整和无效变体。在后者的基因座中,无效等位基因在高加索人中的频率高于俾格米人,这表明非洲人群可能具有更大的功能性OR基因库。有趣的是,在分析整个OR编码区时,我们发现在高加索人样本的许多基因座上高频衍生等位基因过量,但在俾格米人样本中则较少。我们的观察结果不太可能由简单的人口模型来解释,而可能是由于对高加索人OR基因座的正选择作用所致。

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