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利用高分辨率芯片对人群中嗅觉受体基因座的拷贝数进行分析,揭示人类嗅觉受体基因座的复杂性。

Unravelling the complexity of human olfactory receptor repertoire by copy number analysis across population using high resolution arrays.

机构信息

Genomics Lab, Department of Studies in Zoology, University of Mysore, Manasagangotri, Mysore, India.

出版信息

PLoS One. 2013 Jul 3;8(7):e66843. doi: 10.1371/journal.pone.0066843. Print 2013.

Abstract

Olfactory receptors (OR), responsible for detection of odor molecules, belong to the largest family of genes and are highly polymorphic in nature having distinct polymorphisms associated with specific regions around the globe. Since there are no reports on the presence of copy number variations in OR repertoire of Indian population, the present investigation in 43 Indians along with 270 HapMap and 31 Tibetan samples was undertaken to study genome variability and evolution. Analysis was performed using Affymetrix Genome-Wide Human SNP Array 6.0 chip, Affymterix CytoScan(®) High-Density array, HD-CNV, and MAFFT program. We observed a total of 1527 OR genes in 503 CNV events from 81.3% of the study group, which includes 67.6% duplications and 32.4% deletions encompassing more of genes than pseudogenes. We report human genotypic variation in functional OR repertoire size across populations and it was found that the combinatorial effect of both "orthologous obtained from closely related species" and "paralogous derived sequences" provide the complexity to the continuously occurring OR CNVs.

摘要

嗅觉受体 (OR) 负责检测气味分子,属于最大的基因家族,在自然界中具有高度多态性,具有与全球特定区域相关的独特多态性。由于目前还没有关于印度人群 OR 基因库中存在拷贝数变异的报道,因此本研究在 43 名印度人和 270 名 HapMap 及 31 名藏族人群中进行,旨在研究基因组的变异性和进化。使用 Affymetrix Genome-Wide Human SNP Array 6.0 芯片、Affymterix CytoScan(®) High-Density array、HD-CNV 和 MAFFT 程序进行了分析。我们在 503 个 CNV 事件中观察到了 1527 个 OR 基因,占研究组的 81.3%,其中包括 67.6%的重复和 32.4%的缺失,涵盖的基因多于假基因。我们报告了人群中功能性 OR 基因库大小的人类基因型变异,发现“来自亲缘关系密切的物种的同源序列”和“衍生序列的旁系同源序列”的组合效应为不断发生的 OR CNVs 提供了复杂性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd61/3700933/9a63d5e37119/pone.0066843.g001.jpg

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