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由人类T细胞受体β链基因中的倒位机制产生的连接多样性连接复合体和可变多样性复合体。

A joining-diversity-joining complex generated by inversion mechanism and a variable-diversity complex in the beta-chain gene of the human T-cell receptor.

作者信息

Ikuta K, Ogura T, Shimizu A, Honjo T

出版信息

Nucleic Acids Res. 1986 Jun 25;14(12):4899-909. doi: 10.1093/nar/14.12.4899.

Abstract

We have analysed an inactive allele of the beta-chain gene of the T-cell receptor in a human T-cell line HPB-ALL. Comparison with germline sequences showed that HPB-ALL has a joining (J)-diversity (D)-J complex recombined in head-to-head configuration and a variable (V)-D complex in tail-to-tail configuration. These results demonstrate that the inversion mechanism functions in the beta-chain gene of the T-cell receptor. The presence of the V-D complex suggests that V-D recombination could occur prior to D-J recombination although there is no definite proof that the V-D complex is an intermediate to form the V-D-J complex.

摘要

我们分析了人类T细胞系HPB-ALL中T细胞受体β链基因的一个无活性等位基因。与种系序列比较显示,HPB-ALL具有以头对头构型重组的连接(J)-多样性(D)-J复合体以及以尾对尾构型的可变(V)-D复合体。这些结果表明,倒位机制在T细胞受体β链基因中起作用。V-D复合体的存在表明V-D重组可能在D-J重组之前发生,尽管没有确凿证据证明V-D复合体是形成V-D-J复合体的中间体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23ef/311499/5ec053b023ff/nar00281-0208-a.jpg

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