Ip H S, Wilson D B, Heikinheimo M, Leiden J M, Parmacek M S
Department of Medicine, University of Chicago, IL, USA.
Adv Exp Med Biol. 1995;382:117-24. doi: 10.1007/978-1-4615-1893-8_13.
The unique contractile phenotype of cardiac myocytes is determined by the expression of a set of cardiac-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. Here, we demonstrate that the slow/cardiac-specific troponin C (cTnC) enhancer contains a specific binding site for the lineage-restricted, zinc finger transcription factor, GATA-4 and that GATA-4 mRNA and protein is expressed in cardiac myocytes. In addition, GATA-4 binding sites were identified in several previously characterized cardiac-specific transcriptional regulatory elements. The cTnC GATA-4 binding site is required for transcriptional enhancer activity in primary cardiac myocytes. Moreover, the cTnC enhancer can be transactivated by over-expression of GATA-4 in non-cardiac muscle cells such as NIH 3T3 cells. Taken together, these results are consistent with a model in which GATA-4 functions to direct tissue-specific gene expression during mammalian cardiac development.
心肌细胞独特的收缩表型由一组心脏特异性基因的表达所决定。类比其他哺乳动物发育系统,心脏基因的协同表达可能受谱系特异性转录因子控制,这些转录因子与这些基因转录调控区域中的启动子和增强子元件相互作用。在此,我们证明慢型/心脏特异性肌钙蛋白C(cTnC)增强子含有谱系限制性锌指转录因子GATA-4的特异性结合位点,并且GATA-4 mRNA和蛋白在心肌细胞中表达。此外,在几个先前已鉴定的心脏特异性转录调控元件中也发现了GATA-4结合位点。cTnC的GATA-4结合位点是原代心肌细胞中转录增强子活性所必需的。而且,在非心肌细胞如NIH 3T3细胞中,cTnC增强子可被GATA-4的过表达反式激活。综上所述,这些结果与一个模型相符,即在哺乳动物心脏发育过程中,GATA-4发挥作用指导组织特异性基因表达。