V(D)J recombination: In vitro coding joint formation

被引:27
作者
WeisGarcia, F
Besmer, E
Sawchuk, DJ
Yu, W
Hu, Y
Cassard, S
Nussenzweig, MC
Cortes, P
机构
[1] ROCKEFELLER UNIV,LAB MOL IMMUNOL,NEW YORK,NY 10021
[2] ROCKEFELLER UNIV,HOWARD HUGHES MED INST,RES LAB,NEW YORK,NY 10021
关键词
D O I
10.1128/MCB.17.11.6379
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Antigen receptor genes are assembled through a mechanism known as V(D)J recombination, which involves two different joining reactions: signal and coding joining. Formation of these joints is essential for antigen receptor assembly as well as maintaining chromosomal integrity, Here we report on a cell-free system for coding joint formation using deletion and inversion recombination substrates. In vitro coding joint formation requires RAG1, RAG2, and heat-labile factors present in the nuclear extract of nonlymphoid cells. Both inversion- and deletion-mediated coding joint reactions produce diverse coding joints, with deletions and P nucleotide addition. We also show that deletion-mediated coding joint formation follows the 12/23 rule and requires the catalytic subunit of DNA-dependent protein kinase.
引用
收藏
页码:6379 / 6385
页数:7
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