A HIGHLY CONSERVED ENHANCER DOWNSTREAM OF THE HUMAN MLC1/3 LOCUS IS A TARGET FOR MULTIPLE MYOGENIC DETERMINATION FACTORS

被引:91
作者
ROSENTHAL, N
BERGLUND, EB
WENTWORTH, BM
DONOGHUE, M
WINTER, B
BOBER, E
BRAUN, T
ARNOLD, HH
机构
[1] BOSTON UNIV,SCH MED,DEPT BIOCHEM,BOSTON,MA 02118
[2] UNIV HAMBURG,SCH MED,DEPT TOXICOL,W-2000 HAMBURG 13,GERMANY
基金
美国国家卫生研究院;
关键词
D O I
10.1093/nar/18.21.6239
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 potent muscle-specific enhancer element, originally described in the rat myosin light chain (MLC) 1/3 locus located downstream of the coding region, is found in an analogous position in the human MLC1/3 gene. When linked to a CAT reporter gene and transfected into muscle or non-muscle cells, the human MLC enhancer directs high levels of muscle-specific gene expression from homologous or heterologous promoters, irrespective of position or orientation relative to the CAT transcription unit. A significant degree of sequence homology (over 85%) in the 3′-f1anking regions of the two MLC genes is restricted to a 200 bp sequence which lies approximately 1.5 kb downstream of the polyadenylatlon site in both species. The human enhancer sequence includes binding sites for human myogenic determination factors containing a common basic helix-loop-helix motif, and it can be trans-activated to varying degrees in non-muscle cells by these factors. This study establishes the MLC enhancer as an evolutionarily conserved, integral component of the MLC1/3 locus which constitutes a novel target for the action of myogenic determination factors. © 1990 Oxford University Press.
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页码:6239 / 6246
页数:8
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