利用公开EST数据鉴定人类primo基因多态性。

Zheng Ye, James M Parry
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引用次数: 1

摘要

人类primo基因是最近发现的一种细胞质蛋白,在细胞周期中p53依赖性G2阻滞的调控中起重要作用。可能影响酶活性的primo基因的遗传变异可能具有生物学和流行病学意义。人类表达序列标签(EST)数据库是一个丰富的资源,可用于快速筛选具有生理意义的蛋白质的潜在多态性。在人类EST序列比对的基础上,我们确定了primo基因3'-非翻译区核苷酸824和839的两个候选多态性。利用等位基因特异性聚合酶链反应(PCR)在高加索人群(n=82)中证实了这些多态性的存在。824位罕见等位基因频率(38.4%)显著高于839位罕见等位基因频率(3.7%)。我们的研究结果表明,人类EST数据可以作为快速识别遗传变异的有价值的来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of polymorphisms in the human Reprimo gene using public EST data.

The human Reprimo gene is a recently identified cytoplasmic protein, which plays an important role in the regulation of p53-dependent G2 arrest of the cell cycle. Genetic variations in the Reprimo gene that may influence enzyme activity can be of both biological and epidemiological significance. The human expressed sequence tag (EST) database is a wealth of resources, which can be used to rapidly screen for potential polymorphisms in proteins of physiological interest. On the basis of the alignment of human EST sequences, we identified two candidate polymorphisms at nucleotides 824 and 839 in the 3'-untranslated region of the Reprimo gene. The presence of these polymorphisms was confirmed in a Caucasian population (n=82) by the use of the allele specific polymerase chain reaction (PCR). The rare allele frequency at position 824 (38.4%) is much higher than rare allele frequency at position 839 (3.7%). Our results suggest that the human EST data may serve as a valuable source for the rapid identification of genetic variation.

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