MEF2C公司
关贸总协定
转录因子
染色质免疫沉淀
MyoD公司
细胞生物学
生物
增强子
分子生物学
Mef2
免疫沉淀
发起人
抄写(语言学)
电箱
基因
基因表达
遗传学
哲学
语言学
作者
Ming‐Xi Zang,Yong Li,Lixiang Xue,Hong‐Ti Jia,Jing Hua
摘要
Abstract An intricate array of cell‐specific multiprotein complexes participate in programs of cell‐specific gene expression through combinatorial interaction with different transcription factors and cofactors. The dHAND basic helix‐loop‐helix (bHLH) transcription factor, which is essential for heart development and extra embryonic structures, is thought to regulate cardiomyocyte‐specific gene expression through combinatorial interactions with other cardiac‐restricted transcription factors such as GATA4 and NKX2.5. Here, we determine that dHAND also interacts with the myocyte enhancer binding factor‐2c (MEF2C) protein, which belongs to MADS‐box transcription factors and is essential for heart development. dHAND and MEF2C synergistically activated expression of the atrial naturetic peptide gene (ANP) in transfected HeLa cells. GST‐pulldown and immunoprecipitation assay demonstrate that full‐length MEF2C protein is able to interact with dHAND in vitro and in vivo, just like MEF2A and bHLH transcription factors MyoD in skeletal muscle cells. In addition, electrophoretic mobility shift assays (EMSAs) demonstrate that MEF2C and dHAND do not influence each other's DNA binding activity. Using chromatin immunoprecipitation (ChIP) analysis in H9c2 cells we show that dHAND interact with MEF2C to form protein complex and bind A/T sequence in promoter of ANP. Taken together with previous observations, these results suggest the existence of large multiprotein transcriptional complex with core DNA binding proteins that physically interact with other transcriptional factors to form favorable conformation to potentiate transcription. © 2004 Wiley‐Liss, Inc.
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