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在墨西哥人群中鉴定LCT基因上游14 kb突变热点区域的新型基因变异。

Identification of novel genetic variants in the mutational hotspot region 14 kb upstream of the LCT gene in a Mexican population.

作者信息

Valencia Liliana, Randazzo Andrés, Engfeldt Peter, Olsson Lovisa A, Chávez Adolfo, Buckland Robert J, Nilsson Torbjörn K, Almon Ricardo

机构信息

a Departamento de Nutrición Aplicada y Educación Nutricional , Instituto Nacional de Ciencias Médicas y Nutrición 'Salvador Zubirán' , Mexico City , Mexico.

b Faculty of Medicine and Health , Örebro University , Örebro , Sweden.

出版信息

Scand J Clin Lab Invest. 2017 Sep;77(5):311-314. doi: 10.1080/00365513.2017.1318445. Epub 2017 Apr 28.

Abstract

Several polymorphic loci linked to lactase persistence (LP) have been described, all located in a small mutational hotspot region far upstream (∼14 kb) of the lactase (LCT) gene. One is typically found in Europeans, LCT -13910C > T, several others are found in East Africans and Arabs, e.g. LCT -13907C > G and LCT -13915T > G. The possibility of similar loci, specific to populations in South and Central America, has not received much attention so far. To identify possible novel polymorphisms in the mutational hotspot region, we sampled 158 subjects from a rural area in South-Central Mexico. DNA was isolated from serum, and Sanger sequencing of a 501 bp region spanning the LCT -13910C > T hotspot was successfully performed in 150 samples. The frequency of the European-type LCT -13910 T-allele was q = 0.202, and 35% of the population was thus lactase-persistent (CT or TT). Sixteen novel genetic variants were found amongst 11 of the subjects, all were heterozygotes: seven of the subjects were also carriers of at least one LCT -13910 T-allele. Thus, the mutational hotspot region is also a hotspot in the rural Mexican population: 11/150 subjects carried a total of 16 previously unknown private mutations but no novel polymorphism was found. The relationship between such novel genetic variants in Mexicans and lactase persistence is worthy of more investigation.

摘要

已描述了几个与乳糖酶持续性(LP)相关的多态性位点,它们都位于乳糖酶(LCT)基因上游很远(约14 kb)的一个小突变热点区域。其中一个常见于欧洲人,即LCT -13910C>T,其他几个则在东非人和阿拉伯人中发现,例如LCT -13907C>G和LCT -13915T>G。到目前为止,南美洲和中美洲人群特有的类似位点的可能性尚未受到太多关注。为了确定突变热点区域中可能存在的新多态性,我们从墨西哥中南部的一个农村地区抽取了158名受试者。从血清中分离出DNA,并成功对150个样本中跨越LCT -13910C>T热点的501 bp区域进行了桑格测序。欧洲型LCT -13910 T等位基因的频率为q = 0.202,因此35%的人群具有乳糖酶持续性(CT或TT)。在11名受试者中发现了16个新的基因变异,均为杂合子:其中7名受试者也是至少一个LCT -13910 T等位基因的携带者。因此,突变热点区域在墨西哥农村人群中也是一个热点:11/150的受试者总共携带了16个先前未知的私人突变,但未发现新的多态性。墨西哥人中这些新的基因变异与乳糖酶持续性之间的关系值得进一步研究。

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