A HORMONE-ENCODING GENE IDENTIFIES A PATHWAY FOR CARDIAC BUT NOT SKELETAL-MUSCLE GENE-TRANSCRIPTION

被引:238
作者
GREPIN, C
DAGNINO, L
ROBITAILLE, L
HABERSTROH, L
ANTAKLY, T
NEMER, M
机构
[1] INST RECH CLIN MONTREAL,DEV & DIFFERENCIAT CARDIAQUES LAB,MONTREAL H2W 1R7,PQ,CANADA
[2] UNIV MONTREAL,DEPT PHARMACOL,MONTREAL H2W 1R7,PQ,CANADA
[3] UNIV MONTREAL,DEPT PATHOL,MONTREAL H2W 1R7,PQ,CANADA
关键词
D O I
10.1128/MCB.14.5.3115
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
In contrast to skeletal muscle, the mechanisms responsible for activation and maintenance of tissue-specific transcription in cardiac muscle remain poorly understood. A family of hormone-encoding genes is expressed in a highly specific manner in cardiac but not skeletal myocytes. This includes the A- and B-type natriuretic peptide (ANP and BNP) genes, which encode peptide hormones with crucial roles in the regulation of blood volume and pressure. Since these genes are markers of cardiac cells, we have used them to probe the mechanisms for cardiac muscle-specific transcription. Cloning and functional analysis of the rat BNP upstream sequences revealed unexpected structural resemblance to erythroid but not to muscle-specific promoters and enhancers, including a requirement for regulatory elements containing GATA moths. A cDNA clone corresponding to a member of the GATA family of transcription factors was isolated from a cardiomyocyte cDNA library. Transcription of this GATA gene is restricted mostly to the heart and is undetectable in skeletal muscle. Within the heart, GATA transcripts are localized in ANP- and BNP-expressing myocytes, and forced expression of the GATA protein in heterologous cells markedly activates transcription from the natural cardiac muscle-specific ANP and BNP promoters. This GATA-dependent pathway defines the first mechanism for cardiac muscle-specific transcription. Moreover, the present findings reveal striking similarities between the mechanisms controlling gene expression in hematopoietic and cardiac cells and may have important implications for studies of cardiogenesis.
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页码:3115 / 3129
页数:15
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