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胸苷酸合成酶增强子区域:印度人群中的新等位基因。

Thymidylate synthase enhancer region: Novel allele in Indians.

作者信息

Dhawan Dipali, Padh Harish

机构信息

a Department of Cellular and Molecular Biology , B. V. Patel PERD Centre , Ahmedabad , India.

出版信息

Ann Hum Biol. 2017 Feb;44(1):87-90. doi: 10.3109/03014460.2016.1170206. Epub 2016 Apr 24.

Abstract

BACKGROUND

Thymidylate synthase (TS) is the major target for fluoropyrimidine drugs like 5-Fluorouracil (5-FU). There are polymorphic tandem repeats in the TYMS gene enhancer region (TSER). The number of tandem repeats varies in different populations. The aim of this study was to determine the frequencies of the TSER tandem repeats (rs34743033) and compare the observed frequencies with those of other populations.

METHODS

This study genotyped 350 healthy individuals by Polymerase Chain Reaction (PCR).

RESULTS

A novel allele 1 (only a single repeat) was observed in four individuals, the individuals were heterozygous (TSER1/*2) for TYMS. Another variant rs2853542 affecting the expression of Thymidylate synthase was also analysed. The observed genotype frequencies were compared with frequencies observed in other populations for understanding differences between various population groups. There was a statistically significant difference between Indians and Chinese, Kenyans, Ghanians, African-Americans, Americans of European Ancestry, British, Hungarians, Turkish, Australians and Brazilians.

CONCLUSION

This study identified a novel single repeat in the TYMS gene which might have an impact on the expression of this gene, which needs to be confirmed by functional studies.

摘要

背景

胸苷酸合成酶(TS)是5-氟尿嘧啶(5-FU)等氟嘧啶类药物的主要作用靶点。胸苷酸合成酶基因增强子区域(TSER)存在多态性串联重复序列。不同人群中串联重复序列的数量有所不同。本研究旨在确定TSER串联重复序列(rs34743033)的频率,并将观察到的频率与其他人群的频率进行比较。

方法

本研究采用聚合酶链反应(PCR)对350名健康个体进行基因分型。

结果

在4名个体中观察到一个新的等位基因1(仅有一个重复序列),这些个体为胸苷酸合成酶基因杂合子(TSER1/*2)。还分析了另一个影响胸苷酸合成酶表达的变体rs2853542。将观察到的基因型频率与其他人群中观察到的频率进行比较,以了解不同人群组之间的差异。印度人与中国人、肯尼亚人、加纳人、非裔美国人、欧洲裔美国人、英国人、匈牙利人、土耳其人、澳大利亚人和巴西人之间存在统计学上的显著差异。

结论

本研究在胸苷酸合成酶基因中鉴定出一个新的单重复序列,其可能对该基因的表达产生影响,这需要通过功能研究加以证实。

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