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胱硫醚β-合酶基因中833T>C、844ins68突变及一种新突变的检测与等位基因频率

Detection and allele-frequencies of the 833T>C, 844ins68 and a novel mutation in the cystathionine beta-synthase gene.

作者信息

Griffioen Pieter H, de Jonge Robert, van Zelst Bertrand D, Montserrate Brouns R, Lindemans Jan

机构信息

Department of Clinical Chemistry Erasmus MC, University Medical Center Rotterdam, P.O. Box 2040, 3000 CA Rotterdam, The Netherlands.

出版信息

Clin Chim Acta. 2005 Apr;354(1-2):191-4. doi: 10.1016/j.cccn.2004.11.019. Epub 2004 Dec 30.

Abstract

BACKGROUND

The most common 833T>C/844ins68 in cis double mutation in the cystathionine beta synthase (CBS) gene probably is non-pathogenic because the 68-bp insertion eliminates the 833T>C mutation due to alternative splicing. However, allele frequency and effects of the isolated 833T>C mutation are unclear.

METHOD

DNA was isolated from 500 volunteers and used directly for PCR-RFLP of CBS gene exon-8. A new primer design was developed to create annealing sites upstream and downstream of exon-8 for forward and reverse primers, respectively. The design was made to exclude sequence homology of the forward primer with the insert fragment and to introduce an internal Bsr1 digestion site.

RESULTS

A new 9276G>A mutation was found in intron 8. Because of this mutation, an extra Bsr1 digestion site is created in intron 8. In Caucasian volunteers, the following allele frequencies were found: 833T>C=0.2%, 833T>C/844ins68=10.2%, and 9276G>A=0.2%.

CONCLUSION

The developed PCR-RFLP method is able to detect the 833T>C mutation, the 833T>C/844ins68 polymorphism as well as a new 9276G>A mutation in intron 8. Further study should explore the effect of the isolated 9276G>A mutation.

摘要

背景

胱硫醚β合酶(CBS)基因中最常见的顺式双突变833T>C/844ins68可能无致病性,因为68bp的插入通过可变剪接消除了833T>C突变。然而,孤立的833T>C突变的等位基因频率和影响尚不清楚。

方法

从500名志愿者中分离DNA,并直接用于CBS基因外显子8的PCR-RFLP分析。开发了一种新的引物设计,分别在外显子8的上游和下游为正向和反向引物创建退火位点。该设计旨在排除正向引物与插入片段的序列同源性,并引入一个内部Bsr1消化位点。

结果

在内含子8中发现了一个新的9276G>A突变。由于该突变,在内含子8中产生了一个额外的Bsr1消化位点。在白种人志愿者中,发现以下等位基因频率:833T>C=0.2%,833T>C/844ins68=10.2%,9276G>A=0.2%。

结论

所开发的PCR-RFLP方法能够检测833T>C突变、833T>C/844ins68多态性以及内含子8中的一个新的9276G>A突变。进一步的研究应探索孤立的9276G>A突变的影响。

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