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源自亚洲人的黑皮质素1受体基因新型功能变异体的鉴定。

Identification of novel functional variants of the melanocortin 1 receptor gene originated from Asians.

作者信息

Nakayama Kazuhiro, Soemantri Augustinus, Jin Feng, Dashnyam Bumbein, Ohtsuka Ryutaro, Duanchang Phaibool, Isa Mohd Nizam, Settheetham-Ishida Wannapa, Harihara Shinji, Ishida Takafumi

机构信息

Department of Biological Sciences, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, 1130033, Tokyo, Japan.

出版信息

Hum Genet. 2006 Apr;119(3):322-30. doi: 10.1007/s00439-006-0141-1. Epub 2006 Feb 4.

Abstract

Human melanocortin 1 receptor (MC1R) is a seven transmembrane G-coupled protein receptor that upregulates the cAMP pathway. Several functional variants of MC1R that show an impaired ability to activate the cAMP pathway are strongly associated with fair skin and red hair in Europeans and European descendants. The sequence variations of the MC1R gene were repeatedly investigated against worldwide populations; however, there was no evidence that functional variant of MC1R exists in non-European descendants. We report the presence of novel functional variants of MC1R with Asian origins. Three novel variants of MC1R, Phe147Delta, Thr157Ile, and Pro159Thr, were identified in our screening for the sequence variations of the MC1R gene against 995 individuals from 30 Asian and Oceanian populations; there was a single case for the Pro159Thr variant allele and two instances of Phe147Delta and Thr157Ile variant alleles. Our pharmacological assay revealed that Phe147Delta, Thr157Ile, and Pro159Thr variant showed similar or more dramatically impaired activities in comparison with Arg151Cys, which is a major functional variant of MC1R in Europeans. These functional variant alleles were geographically localized in relatively high latitudes, which suggest that the adaptation to ambient UV light intensity may play an important role in shaping the geographical distribution of MC1R alleles in Asia and Oceania.

摘要

人类黑皮质素1受体(MC1R)是一种七跨膜G蛋白偶联受体,可上调cAMP信号通路。MC1R的几种功能变体表现出激活cAMP信号通路的能力受损,这与欧洲人和欧洲后裔的白皙皮肤和红发密切相关。针对全球人群对MC1R基因的序列变异进行了反复研究;然而,没有证据表明非欧洲后裔中存在MC1R的功能变体。我们报告了源自亚洲的新型MC1R功能变体的存在。在对来自30个亚洲和大洋洲人群的995名个体进行MC1R基因序列变异筛查时,鉴定出了三种新型MC1R变体,即Phe147Delta、Thr157Ile和Pro159Thr;Pro159Thr变体等位基因有1例,Phe147Delta和Thr157Ile变体等位基因各有2例。我们的药理学分析表明,与Arg151Cys(欧洲人MC1R的主要功能变体)相比,Phe147Delta、Thr157Ile和Pro159Thr变体的活性受损程度相似或更显著。这些功能变体等位基因在地理上集中在相对较高的纬度地区,这表明对环境紫外线强度的适应可能在塑造亚洲和大洋洲MC1R等位基因的地理分布中起重要作用。

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