An essential octamer motif in the mb-1 (Igα) promoter

被引:12
作者
Malone, CS
Patrone, L
Wall, R
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Microbiol & Immunol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Sch Med, Inst Mol Biol, Los Angeles, CA 90095 USA
关键词
mb-1; Ig alpha; B29; Ig beta; Oct-1; Oct-2; transcription; gene regulation; promoter;
D O I
10.1016/S0161-5890(00)00045-6
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
The mb-1 (Ig alpha) gene is B cell-specific and expressed throughout B cell maturation. In combination with B29 (Ig beta) and surface immunoglobulin mb-1 comprises the B cell receptor complex (BCR). The murine mb-1 promoter has been characterized to depend on the trans-acting transcription factors; Sp1, ets, Ikaros, and EBF for full promoter activity. These trans-acting factors are also involved in the regulation of mb-1's closely related heterodimeric partner, B29. However, octamer transcription factors 1 and 2 (Oct-1 and Oct-2) are also necessary for full B29 promoter activity while they are not known to be required for mb-1 promoter activity. Here, we show that the octamer transcription factors bind a degenerate octamer consensus sequence within the mb-1 promoter. Like B29, the mb-1 octamer-binding, motif interacted with both ubiquitously expressed Oct-1 and the B cell-specific Oct-2 transcription factors. Furthermore, the interaction of Oct-1 and Oct-2 contributed to the regulation of the mb-1 promoter as site-directed mutations within the octamer motif substantially reduced its activity. These data confirm that octamer factor interactions and function contribute to the full transcriptional activity of the mb-1 promoter. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:321 / 328
页数:8
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