THE GATA-4 TRANSCRIPTION FACTOR TRANSACTIVATES THE CARDIAC MUSCLE-SPECIFIC TROPONIN-C PROMOTER-ENHANCER IN NONMUSCLE CELLS

被引:162
作者
IP, HS
WILSON, DB
HEIKINHEIMO, M
TANG, ZH
TING, CN
SIMON, MC
LEIDEN, JM
PARMACEK, MS
机构
[1] UNIV CHICAGO,DEPT MED,CHICAGO,IL 60637
[2] UNIV CHICAGO,DEPT MOLEC GENET & CELL BIOL,CHICAGO,IL 60637
[3] UNIV CHICAGO,DEPT PATHOL,CHICAGO,IL 60637
[4] UNIV CHICAGO,HOWARD HUGHES MED INST,CHICAGO,IL 60637
[5] WASHINGTON UNIV,SCH MED,DEPT PEDIAT,ST LOUIS,MO 63110
[6] WASHINGTON UNIV,SCH MED,DEPT MOLEC BIOL & PHARMACOL,ST LOUIS,MO 63110
[7] UNIV HELSINKI,CHILDRENS HOSP,HELSINKI,FINLAND
关键词
D O I
10.1128/MCB.14.11.7517
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 unique contractile phenotype of cardiac myocytes is determined by the expression of a set of cardiac muscle-specific genes. By analogy to other mammalian developmental systems, it is likely that the coordinate expression of cardiac genes is controlled by lineage-specific transcription factors that interact with promoter and enhancer elements in the transcriptional regulatory regions of these genes. Although previous reports have identified several cardiac muscle-specific transcriptional elements, relatively little is known about the lineage-specific transcription factors that regulate these elements. In this report, we demonstrate that the slow/cardiac muscle-specific troponin C (cTnC) enhancer contains a specific binding site for the lineage-restricted zinc finger transcription factor GATA-4 This GATA-4-binding site is required for enhancer activity in primary cardiac myocytes. Moreover, the cTnC enhancer can be transactivated by overexpression of GATA-4 in non-cardiac muscle cells such as NIH 3T3 cells. In situ hybridization studies demonstrate that GATA-4 and cTnC have overlapping patterns of expression in the hearts of postimplantation mouse embryos and that GATA-4 gene expression precedes cTnC expression. Indirect immunofluorescence reveals GATA-4 expression in cultured cardiac myocytes from neonatal rats. Taken together, these results are consistent with a model in which GATA-4 functions to direct tissue-specific gene expression during mammalian cardiac development.
引用
收藏
页码:7517 / 7526
页数:10
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