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RAG1和RAG2蛋白在V(D)J重组中确立了12/23规则。

The RAG1 and RAG2 proteins establish the 12/23 rule in V(D)J recombination.

作者信息

van Gent D C, Ramsden D A, Gellert M

机构信息

Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Cell. 1996 Apr 5;85(1):107-13. doi: 10.1016/s0092-8674(00)81086-7.

Abstract

V(D)J recombination requires a pair of signal sequences with spacer lengths of 12 and 23 base pairs. Cleavage by the RAG1 AND RAG2 proteins was previously shown to demand only a single signal sequence. Here, we established conditions where 12- and 23-spacer signal sequences are both necessary for cleavage. Coupled cutting at both sites requires only the RAG1 and RAG2 proteins, but depends on the metal ion. In Mn2+, a single signal sequence supports efficient double strand cleavage, but cutting in Mg2+ requires two signal sequences and is best with the canonical 12/23 pair. Thus, the RAG proteins determine both aspects of the specificity of V(D)J recombination, the recognition of a single signal sequence and the correct 12/23 coupling in a pair of signals.

摘要

V(D)J重排需要一对间隔长度分别为12和23个碱基对的信号序列。此前研究表明,RAG1和RAG2蛋白的切割仅需要单个信号序列。在此,我们建立了这样的条件:12间隔和23间隔的信号序列对于切割都是必需的。两个位点的偶联切割仅需要RAG1和RAG2蛋白,但依赖于金属离子。在Mn2+中,单个信号序列就能支持高效的双链切割,但在Mg2+中切割需要两个信号序列,并且在标准的12/23对时效果最佳。因此,RAG蛋白决定了V(D)J重排特异性的两个方面,即单个信号序列的识别以及一对信号中正确的12/23偶联。

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