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抗体多样性的种系基础。

Germ line basis for antibody diversity.

作者信息

Williamson A R, Premkumar E, Shoyab M

出版信息

Fed Proc. 1975 Jan;34(1):28-32.

PMID:803236
Abstract

Each antibody polypeptide chain is the product of a gene pair comprising one constant (C) gene coding for that portion of the chain common to all chains of the same type and one variable (V) gene coding for the sequence unique to each chain. Previous evidence indicates that the haploid genome has a single copy of each distinct C gene and that for expression a gene pair is formed with any one of a family of V genes present in the same haploid genome. Hybridization of purified mRNA coding for immunoglobulin heavy chain (mRNA-H) with a vast excess of DNA confirms the existence of a single C gene of each type and multiple V genes. A large number (of the order of 104) of V genes would be consistent with the hybridization results. This suggests considerable V gene redundancy which is a predictable property of a multiple V gene family maintained by expansion and contraction mechanisms. The mRNA-H used in these hybridization studies was isolated by a specific interaction with immunoglobulin. The same method has also been used to isolate a nuclear precursor of mRNA-H. Identification of this precursor strengthens the evidence for the direct joining of the V and C gene pair at the DNA level prior to transcription.

摘要

每条抗体多肽链都是一个基因对的产物,该基因对包括一个恒定(C)基因,其编码同一类型所有链共有的链的那部分,以及一个可变(V)基因,其编码每条链特有的序列。先前的证据表明,单倍体基因组对每个不同的C基因都有一个拷贝,并且为了表达,基因对是由同一单倍体基因组中存在的V基因家族中的任何一个形成的。编码免疫球蛋白重链的纯化mRNA(mRNA-H)与大量过量的DNA杂交,证实了每种类型都存在单个C基因和多个V基因。大量(约104个)V基因与杂交结果一致。这表明存在相当大的V基因冗余,这是由扩增和收缩机制维持的多个V基因家族的可预测特性。这些杂交研究中使用的mRNA-H是通过与免疫球蛋白的特异性相互作用分离的。同样的方法也被用于分离mRNA-H的核前体。这种前体的鉴定加强了在转录之前V基因对和C基因对在DNA水平直接连接的证据。

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