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心脏转录因子GATA4和Nkx2.5对Id2表达的诱导作用。

Induction of Id2 expression by cardiac transcription factors GATA4 and Nkx2.5.

作者信息

Lim Joong-Yeon, Kim Won Ho, Kim Joon, Park Sang Ick

机构信息

Division of Intractable Diseases, Center for Biomedical Sciences, National Institute of Health, 194, Tongillo, Eunpyeong-gu, Seoul 122-701, Korea.

出版信息

J Cell Biochem. 2008 Jan 1;103(1):182-94. doi: 10.1002/jcb.21396.

Abstract

Inhibitor of differentiation/DNA binding (Id) proteins function as a regulator of helix-loop-helix proteins participating in cell lineage commitment and differentiation. Here, we observed a marked induction of Id2 during cardiomyocyte differentiation from P19CL6 murine embryonic teratocarcinoma stem cells, prompting us to investigate the upstream regulatory mechanism of Id2 induction. Computer analysis of Id2 promoter and subsequent electrophoretic mobility shift assay revealed several binding sites for GATA4 and Nkx2.5 within the Id2 promoter. By further deletion and mutation analysis of the respective binding site, we identified that two motifs located at -497/-502 and -264/-270 were functionally important for Id2 promoter activation by GATA4 and Nkx2.5, respectively. Overexpression of GATA4 and/or Nkx2.5 induced not only Id2 promoter activity but also Id2 protein expression. Additionally, Id proteins significantly inhibit the GATA4 and Nkx2.5-dependent transcription, suggesting Id proteins may play a regulatory role in cardiogenesis. Collectively, our results demonstrate that GATA4 and Nkx2.5 could be one of the upstream regulators of Id2.

摘要

分化/DNA结合抑制因子(Id)蛋白作为一种调节因子,参与细胞谱系定向和分化过程中的螺旋-环-螺旋蛋白的调控。在此,我们观察到在P19CL6小鼠胚胎性癌细胞干细胞向心肌细胞分化过程中,Id2有明显的诱导现象,这促使我们研究Id2诱导的上游调控机制。对Id2启动子进行计算机分析并随后进行电泳迁移率变动分析,结果显示Id2启动子内存在多个GATA4和Nkx2.5的结合位点。通过对各个结合位点进行进一步的缺失和突变分析,我们确定位于-497/-502和-264/-270的两个基序分别对GATA4和Nkx2.5激活Id2启动子具有重要功能。GATA4和/或Nkx2.5的过表达不仅诱导了Id2启动子活性,还诱导了Id2蛋白表达。此外,Id蛋白显著抑制GATA4和Nkx2.5依赖的转录,提示Id蛋白可能在心脏发生过程中发挥调节作用。总之,我们的结果表明GATA4和Nkx2.5可能是Id2的上游调节因子之一。

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