The 3' enhancer region determines the B/T specificity and pro-B pre-B specificity of immunoglobulin V-kappa-J(kappa) joining

被引:57
作者
Hiramatsu, R
Akagi, K
Matsuoka, M
Sakumi, K
Nakamura, H
Kingsbury, L
David, C
Hardy, RR
Yamamura, K
Sakano, H
机构
[1] KUMAMOTO UNIV, SCH MED, INST MOLEC EMBRYOL & GENET, DEPT DEV GENET, KUMAMOTO 862, JAPAN
[2] MAYO CLIN & MAYO FDN, DEPT IMMUNOL, ROCHESTER, MN 55905 USA
[3] FOX CHASE CANC CTR, INST CANC RES, PHILADELPHIA, PA 19111 USA
[4] UNIV TOKYO, GRAD SCH SCI, DEPT BIOPHYS & BIOCHEM, BUNKYO KU, TOKYO 113, JAPAN
基金
美国国家卫生研究院;
关键词
D O I
10.1016/0092-8674(95)90138-8
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
Using transgenic substrates, we found that the immunoglobulin kappa gene 3' enhancer (E3') acts as a negative regulator in V-kappa-J(kappa) joining. Although the E3' was originally identified as a transcriptional enhancer, it acts in a suppressive manner for recombinational regulation. Base substitution analysis has shown that the PU.1-binding site within the E3' regulates the B/T specificity of V-kappa-J(kappa) joining. In a substrate with a mutated PU.1-binding site (GAGGAA to TCTTCG), V-kappa-J(kappa) joining occurred not only in B cells, but also in T cells. The E3' region is also responsible for determining the pro-B/pre-B specificity of V-kappa-J(kappa) joining. When the E3' region was deleted, kappa gene rearrangement actively occurred at the early pro-B stage of B cell development: nongermline (N) nucleotides were common at recombination junctions.
引用
收藏
页码:1113 / 1123
页数:11
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