人类RD基因的结构:一个高度保守的基因,位于主要组织相容性复合体的III类区域。

P W Speiser, P C White
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引用次数: 22

摘要

我们克隆并确定了一个新基因(称为RD或D6S45)的DNA序列,该基因位于人类主要组织相容性复合体(HLA)的III类区域,位于Bf和C4A补体基因之间。该基因的编码区包含在10个外显子中,分布在大约6 kb的DNA上。该编码蛋白预计含有371个氨基酸残基,分子量为41,000。预测的氨基酸序列值得注意的是,中心区域包含24对连续交替的碱性(Arg)和酸性(Asp或Glu)残基,与U1小核糖核酸(snRNP)的70K蛋白相似,但更严格地交替。人RD基因与鼠RD基因在氨基酸和DNA水平上具有高度的同源性。虽然中心区域是高度重复的,并且含有高比例(13%)的CpG二核苷酸,这两种特征都可能导致频繁的突变,但对来自6个个体的基因的该区域的序列分析显示没有多态性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structure of the human RD gene: a highly conserved gene in the class III region of the major histocompatibility complex.

We cloned and determined the DNA sequence of a novel gene (termed RD or D6S45) situated in the class III region of the human major histocompatibility complex (HLA) between the Bf and C4A complement genes. The coding region of the gene is contained in 10 exons spread over approximately 6 kb of DNA. The encoded protein is predicted to contain 371 amino acid residues with a molecular weight of 41,000. The predicted amino acid sequence is notable for a central region containing 24 consecutive pairs of alternating basic (Arg) and acidic (Asp or Glu) residues similar to, but more strictly alternating than, those seen in the 70K protein of the U1 small nuclear ribonucleoprotein (snRNP). There is a high degree of homology both at the amino acid and DNA level between the human RD gene and its murine homology. Although the central region is highly repetitious and contains a high proportion (13%) of CpG dinucleotides-both features that might predispose to frequent mutations-sequence analysis of this region in genes amplified from six individuals revealed no polymorphism.

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