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在健康亚洲人中检测到人类胱硫醚β-合酶(CBS)基因中31bp VNTR多态性的新等位基因。

Novel alleles of 31-bp VNTR polymorphism in the human cystathionine β-synthase (CBS) gene were detected in healthy Asians.

作者信息

Gan Yik-Yuen, Chen Chuan-Fei

机构信息

Natural Sciences and Science Education, National Institute of Education, Nanyang Technological University,1 Nanyang Walk, Singapore 637616, Republic of Singapore.

出版信息

J Genet. 2010 Dec;89(4):449-55. doi: 10.1007/s12041-010-0063-5.

Abstract

A 31-bp variable number of tandem repeats (VNTR) polymorphism of the cystathionine β-synthase (CBS) gene was earlier reported in Caucasians of predominantly European descent and Indo-Caucasoid populations. We report here for the first time, the detection of allele 20, which was absent in Caucasian and Indo-Caucasoid populations, as a common allele present in Singaporean Chinese (6.25%), Indians (11.7%), and Malays (11.5%). Hence, allele 20 might be a specific allele for Asian populations. A relatively common allele 19 found in the Caucasian and Indo-Caucasoid populations (10.4%-10.6%) was absent in the Asian samples of this study. Therefore, allele 19 might be a specific allele for the Caucasian populations. A novel and rare allele 13, which was not reported before in the Caucasian and Indo-Caucasoid populations, was found in 0.5% of Singaporean Chinese as genotype 13/17 heterozygotes. The presence of alleles 13 and 20 were verified by DNA sequencing. There were five new genotypes (13/17, 16/20, 17/20, 18/20 and 20/20) not reported before in the Caucasian and Indo-Caucasoid populations, detected in this study. Nine genotypes (15/18, 16/18, 16/21, 17/19, 18/19, 18/21, 19/19, 19/21 and 21/21) which were present in the Caucasian and/or Indo-Caucasoid populations were absent in this study. Our results showed that CBS 31-bp VNTR polymorphism has a distinct genetic difference in allele and genotype frequencies between the European Caucasians, Indo-Caucasoid and Asian populations.

摘要

早期报道了胱硫醚β合酶(CBS)基因31个碱基对的可变串联重复序列(VNTR)多态性,该报道主要针对欧洲血统的白种人和印度 - 高加索人群。我们首次在此报告,检测到等位基因20,其在白种人和印度 - 高加索人群中不存在,却是新加坡华人(6.25%)、印度人(11.7%)和马来人(11.5%)中的常见等位基因。因此,等位基因20可能是亚洲人群的特异性等位基因。在白种人和印度 - 高加索人群中发现的相对常见的等位基因19(10.4% - 10.6%)在本研究的亚洲样本中不存在。因此,等位基因19可能是白种人群的特异性等位基因。一种新的罕见等位基因13,此前在白种人和印度 - 高加索人群中未被报道,在0.5%的新加坡华人中以13/17杂合子基因型被发现。等位基因13和20的存在通过DNA测序得到验证。本研究检测到五种在白种人和印度 - 高加索人群中未被报道过的新基因型(13/17、16/20、17/20、18/20和20/20)。九种存在于白种人和/或印度 - 高加索人群中的基因型(15/18、16/18、16/21、17/19、18/19、18/21、19/19、19/21和21/21)在本研究中不存在。我们的结果表明,CBS基因31个碱基对的VNTR多态性在欧洲白种人、印度 - 高加索人和亚洲人群的等位基因和基因型频率上存在明显的遗传差异。

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