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TBX5与MEF2C之间的物理相互作用是早期心脏发育所必需的。

Physical interaction between TBX5 and MEF2C is required for early heart development.

作者信息

Ghosh Tushar K, Song Fei Fei, Packham Elizabeth A, Buxton Sarah, Robinson Thelma E, Ronksley Jonathan, Self Tim, Bonser Andrew J, Brook J David

机构信息

Institute of Genetics, School of Biology, University of Nottingham, Queen's Medical Centre, Nottingham, United Kingdom.

出版信息

Mol Cell Biol. 2009 Apr;29(8):2205-18. doi: 10.1128/MCB.01923-08. Epub 2009 Feb 9.

Abstract

TBX5 is a transcription factor which plays important roles in the development of the heart and upper limbs. Mutations in this gene produce the inherited disorder Holt-Oram syndrome. Here, we report a physical interaction between TBX5 and MEF2C leading to a synergistic activation of the alpha-cardiac myosin heavy chain (MYH6). Mutants of TBX5, TBX5G80R, and TBX5R279X that produce severe cardiac phenotypes impair the synergy. Using fluorescence resonance energy transfer, we demonstrate the interaction of TBX5 and MEF2C in living cells. We also show that they physically associate through their DNA-binding domains to form a complex on the MYH6 promoter. Morpholino-mediated knockdowns of Tbx5 and Mef2c in zebrafish suggest that the genetic interaction of these proteins is not only required for MYH6 expression but also essential for the early stages of heart development and survival. This is the first report of a functional interaction between a T-box protein and a MADS box factor that may be crucial in cardiomyocyte differentiation.

摘要

TBX5是一种转录因子,在心脏和上肢发育中发挥重要作用。该基因的突变会导致遗传性疾病 Holt-Oram 综合征。在此,我们报告了TBX5与MEF2C之间的物理相互作用,这种相互作用导致α-心肌肌球蛋白重链(MYH6)的协同激活。产生严重心脏表型的TBX5突变体TBX5G80R和TBX5R279X会损害这种协同作用。利用荧光共振能量转移技术,我们证明了TBX5与MEF2C在活细胞中的相互作用。我们还表明,它们通过其DNA结合结构域在物理上相互关联,在MYH6启动子上形成复合物。在斑马鱼中通过吗啉代介导的Tbx5和Mef2c敲低表明,这些蛋白质的遗传相互作用不仅是MYH6表达所必需的,而且对心脏发育和存活的早期阶段也至关重要。这是关于T-box蛋白与MADS盒因子之间功能相互作用的首次报道,这种相互作用可能在心肌细胞分化中起关键作用。

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