GATA-dependent regulation of TPO-induced c-mpl gene expression during megakaryopoiesis.

Masataka Sunohara, Shigeru Morikawa, Akira Fuse, Iwao Sato
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引用次数: 2

Abstract

Thrombopoietin (TPO) and its receptor, c-Mpl, play the crucial role during megakaryocytopoiesis. Previously, we have shown that the promoter activity of c-mpl induced by TPO is modulated by transcription through a PKC-dependent pathway and that GATA(-77) is involved as a positive regulatory element in TPO-induced c-mpl gene expression in the megakaryoblastic CMK cells. In this research, to examine participating possibility of GATA promoter element in TPO- induced c-mpl gene expression through a PKC-independent pathway, the promoter activity of site-directed mutagenesis and the effect of potein kinase C modulator were measured by a transient transfection assay system. Together with our previous results on the TPO-induced c-mpl promoter, this study indicates destruction of -77GATA in c-mpl promoter decreased the activity by 47.3% under existence of GF109203. These results suggest that GATA promoter element plays significant role in TPO-induced c-mpl gene expression through a PKC-independent pathway.

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巨核形成过程中tpo诱导的c-mpl基因表达的gata依赖性调控。
血小板生成素(TPO)及其受体c-Mpl在巨核细胞生成过程中起着至关重要的作用。在此之前,我们已经证明TPO诱导的c-mpl启动子活性是通过pkc依赖途径通过转录调节的,并且GATA(-77)作为正调控元件参与了巨核母细胞CMK中TPO诱导的c-mpl基因表达。为了研究GATA启动子元件通过pkc非依赖性途径参与TPO诱导的C- mpl基因表达的可能性,本研究采用瞬时转染实验系统检测了位点定向诱变启动子活性和蛋白激酶C调节剂的作用。结合我们之前对tpo诱导的c-mpl启动子的研究结果,本研究表明,在GF109203存在的情况下,c-mpl启动子中-77GATA的破坏使其活性降低了47.3%。这些结果表明GATA启动子元件通过pkc非依赖性途径在tpo诱导的c-mpl基因表达中发挥重要作用。
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