A NOVEL B-CELL DERIVED COACTIVATOR POTENTIATES THE ACTIVATION OF IMMUNOGLOBULIN PROMOTERS BY OCTAMER-BINDING TRANSCRIPTION FACTORS

被引:252
作者
LUO, Y
FUJII, H
GERSTER, T
ROEDER, RG
机构
[1] Laboratory of Biochemistry, Molecular Biology The Rockefeller University New York
基金
美国国家卫生研究院;
关键词
D O I
10.1016/0092-8674(92)90352-D
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
A novel B cell-restricted activity, required for high levels of octamer/Oct-dependent transcription from an immunoglobulin heavy chain (IgH) promoter, was detected in an in vitro system consisting of HeLa cell-derived extracts complemented with fractionated B cell nuclear proteins. The factor responsible for this activity was designated Oct coactivator from B cells (OCA-B). OCA-B stimulates the transcription from an IgH promoter in conjunction with either Oct-1 or Oct-2 but shows no significant effect on the octamer/Oct-dependent transcription of the ubiquitously expressed histone H2B promoter and the transcription of USF- and Sp1-regulated promoters. Taken together, our results suggest that OCA-B is a tissue-, promoter-, and factor-specific coactivator and that OCA-B may be a major determinant for B cell-specific activation of immunoglobulin promoters. In light of the evidence showing physical and functional interactions between Oct factors and OCA-B, we propose a mechanism of action for OCA-B and discuss the implications of OCA-B for the transcriptional regulation of other tissue-specific promoters.
引用
收藏
页码:231 / 241
页数:11
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