EXPRESSION OF A HUMAN 7S-K RNA GENE INVIVO REQUIRES A NOVEL POL-III UPSTREAM ELEMENT

被引:36
作者
KLEINERT, H
BREDOW, S
BENECKE, BJ
机构
关键词
7S K RNA transcription; CACCC-motif; distal sequence element (DSE); footprinting analysis;
D O I
10.1002/j.1460-2075.1990.tb08164.x
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 5'-flanking sequences required for expression of a human 7S K RNA gene have been defined by mutant analysis. A -111 upstream deletion mutant showed full activity when analysed by in vitro transcription with HeLa cell extracts. In contrast, upon transfection into intact cells, this mutant only revealed a basal level activity of ~ 6% as compared to the wild-type promoter up to position -252. The deleted upstream sequence element acts as a transcriptional activator in vivo, in a strictly position and orientation-dependent manner. Two octamer-like binding motifs observed within this upstream sequence were both dispensable for proper function of this RNA polymerase III promoter in vivo. Instead, a detailed analysis of this region identified a CACCC-box element, together with its surrounding base pairs, as the essential upstream element required for expression of this 7S K RNA gene in vivo. Furthermore, this CACCC-box is centered within a footprint obtained with HeLa cell nuclear proteins.
引用
收藏
页码:711 / 718
页数:8
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