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人类补体第四成分的遗传性结构多态性。

Inherited structural polymorphism of the fourth component of human complement.

作者信息

Awdeh Z L, Alper C A

出版信息

Proc Natl Acad Sci U S A. 1980 Jun;77(6):3576-80. doi: 10.1073/pnas.77.6.3576.

Abstract

Human fourth component of complement (C4) was found to be highly polymorphic by agarose gel electrophoresis of neuraminidase-treated plasma. The system allows clear-cut separation of the products of the two C4 genetic loci, C4A (acidic or Rodgers) and C4B (basic or Chido). There are at least six structural variants and a deletion allele at the C4A locus and two structural variants and a deletion allele at the C4B locus. Close linkage with no crossovers was found between the two C4 loci, allowing the definition of C4AB haplotypes, and between C4 haplotypes and the C2 and BF loci of the human histocompatibility complex. Nine C4 haplotypes, each with a frequency of 0.005 or more in Caucasians, were found. These studies provide direct evidence for two distinct but closely linked genetic loci for human C4 in the major histocompatibility complex on the short arm of chromosome 6.

摘要

通过对神经氨酸酶处理的血浆进行琼脂糖凝胶电泳,发现人类补体第四成分(C4)具有高度多态性。该系统能够清晰分离两个C4基因座C4A(酸性或Rodgers型)和C4B(碱性或Chido型)的产物。C4A基因座至少有六个结构变体和一个缺失等位基因,C4B基因座有两个结构变体和一个缺失等位基因。发现两个C4基因座之间紧密连锁且无交叉,从而能够定义C4AB单倍型,以及C4单倍型与人类组织相容性复合体的C2和BF基因座之间的关系。在高加索人中发现了九种C4单倍型,每种单倍型的频率均为0.005或更高。这些研究为位于6号染色体短臂主要组织相容性复合体中的人类C4的两个不同但紧密连锁的基因座提供了直接证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9f3/349660/22988c2119c7/pnas00493-0520-a.jpg

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