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人类内披蛋白基因中由于重复序列数量可变而导致的多态性。

Polymorphism due to variable number of repeats in the human involucrin gene.

作者信息

Simon M, Phillips M, Green H

机构信息

Department of Cellular and Molecular Physiology, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

Genomics. 1991 Apr;9(4):576-80. doi: 10.1016/0888-7543(91)90349-j.

Abstract

The coding region of the involucrin gene in higher primates contains a segment consisting of numerous tandem repeats of a 10-codon sequence. The process of repeat addition began in a common ancestor of all higher primates and subsequent repeats were added vectorially. As a result, the principal site of repeat addition has moved in the 3' to 5' direction and the most recently generated repeats (the late region) are close to the 5' end of the segment of repeats. In the human, most of the late region is made up of two different blocks, each consisting of nearly identical repeats. We describe here five polymorphic forms resulting from the addition of differing numbers of repeats to each block. As the variety and nature of the polymorphic alleles are different in different human populations, we postulate that the process of repeat addition is genetically determined.

摘要

高等灵长类动物中兜甲蛋白基因的编码区包含一段由一个10密码子序列的众多串联重复组成的片段。重复添加过程始于所有高等灵长类动物的一个共同祖先,随后的重复以向量方式添加。结果,重复添加的主要位点已从3'端向5'端移动,最近产生的重复(晚期区域)靠近重复片段的5'端。在人类中,大部分晚期区域由两个不同的模块组成,每个模块由几乎相同的重复序列构成。我们在此描述了由于向每个模块添加不同数量的重复而产生的五种多态形式。由于多态等位基因的种类和性质在不同人群中有所不同,我们推测重复添加过程是由基因决定的。

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