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GATA-4转录因子可在非肌肉细胞中转录激活心肌特异性肌钙蛋白C启动子-增强子。

The GATA-4 transcription factor transactivates the cardiac muscle-specific troponin C promoter-enhancer in nonmuscle cells.

作者信息

Ip H S, Wilson D B, Heikinheimo M, Tang Z, Ting C N, Simon M C, Leiden J M, Parmacek M S

机构信息

Department of Medicine, University of Chicago, IL 60637.

出版信息

Mol Cell Biol. 1994 Nov;14(11):7517-26. doi: 10.1128/mcb.14.11.7517-7526.1994.

Abstract

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.

摘要

心肌细胞独特的收缩表型由一组心肌特异性基因的表达所决定。类比于其他哺乳动物的发育系统,心肌基因的协同表达很可能受谱系特异性转录因子的控制,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。尽管先前的报道已鉴定出几种心肌特异性转录元件,但对于调控这些元件的谱系特异性转录因子却知之甚少。在本报告中,我们证明慢型/心肌特异性肌钙蛋白C(cTnC)增强子含有谱系限制锌指转录因子GATA-4的特异性结合位点。该GATA-4结合位点是原代心肌细胞中增强子活性所必需的。此外,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。原位杂交研究表明,GATA-4和cTnC在植入后小鼠胚胎心脏中的表达模式重叠,且GATA-4基因表达先于cTnC表达。间接免疫荧光显示新生大鼠培养的心肌细胞中有GATA-4表达。综上所述,这些结果与一个模型相符,即GATA-4在哺乳动物心脏发育过程中发挥作用以指导组织特异性基因表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69b8/359288/ff01c2f696a8/molcellb00011-0494-a.jpg

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