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人类补体成分C4的多态性

Polymorphism of human complement component C4.

作者信息

Belt K T, Yu C Y, Carroll M C, Porter R R

出版信息

Immunogenetics. 1985;21(2):173-80. doi: 10.1007/BF00364869.

Abstract

An assessment has been made of the polymorphism of human complement component C4 by comparing derived amino acid sequences of cDNA and genomic DNA with limited amino acid sequences. In all, one complete and six partial sequences have been obtained from material from three individuals and include two C4A and two C4B alleles. Differences were found between the 4 alleles from 2 loci in only 15 of the 1722 amino acid residues, and 12 lie within one section of 230 residues, which in 1 allele also contains a 3-residue deletion. In three variable positions, an allelic difference in one C4 type was common to the other types. Three nucleotide differences were found in four introns. In spite of marked differences in their chemical reactivity, the many allelic forms appear to differ in less than 1% of their amino acid residue positions. This unusual pattern of polymorphism may be due to recent duplication of the C4 gene, or may have arisen by selection as a result of the biological role of C4, which interacts in the complement sequence with nine other proteins necessitating conservation of much of the surface structure.

摘要

通过将cDNA和基因组DNA推导的氨基酸序列与有限的氨基酸序列进行比较,对人类补体成分C4的多态性进行了评估。总共从三个个体的材料中获得了一个完整序列和六个部分序列,包括两个C4A和两个C4B等位基因。在1722个氨基酸残基中,仅15个残基在来自两个位点的4个等位基因之间存在差异,其中12个位于230个残基的一个区域内,在一个等位基因中该区域还存在一个3个残基的缺失。在三个可变位置,一种C4类型的等位基因差异在其他类型中也很常见。在四个内含子中发现了三个核苷酸差异。尽管它们的化学反应性存在显著差异,但许多等位基因形式的氨基酸残基位置差异不到1%。这种不寻常的多态性模式可能是由于C4基因最近发生了复制,或者可能是由于C4在补体序列中与其他九种蛋白质相互作用,需要保留大部分表面结构,从而通过选择产生的。

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