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首页> 外文期刊>Human Molecular Genetics >Zebrafish cul4a, but not cul4b, modulates cardiac and forelimb development by upregulating tbx5a expression
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Zebrafish cul4a, but not cul4b, modulates cardiac and forelimb development by upregulating tbx5a expression

机译:斑马鱼cul4a而非cul4b通过上调tbx5a表达来调节心脏和前肢的发育

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摘要

CUL4A and CUL4B are closely related cullin family members and can each assemble a Cullin-RING E3 ligase complex (CRL) and participate in a variety of biological processes. While the CRLs formed by the two cullin members may have common targets, the two appeared to have very different consequences when mutated or disrupted in mammals. We here investigated the roles of cul4a and cul4b during zebrafish embryogenesis by using the morpholino knockdown approach. We found that cul4a is essential for cardiac development as well as for pectoral fin development. Whereas cul4a morphants appeared to be unperturbed in chamber specification, they failed to undergo heart looping. The failures in heart looping and pectoral fin formation in cul4a morphants were accompanied by greatly reduced proliferation of cardiac cells and pectoral fin-forming cells. We demonstrated that tbx5a, a transcription factor essential for heart and limb development, is transcriptionally upregulated by cul4a and mediates the function of cul4a in cardiac and pectoral fin development. In contrast to the critical importance of cul4a, cul4b appeared to be dispensable for zebrafish development and was incapable of compensating for the loss of cul4a. This work provides the first demonstration of an essential role of cul4a, but not cul4b, in cardiac development and in the regulation of tbx5a in zebrafish. These findings justify exploring the functional role of CUL4A in human cardiac development.
机译:CUL4A和CUL4B是紧密相关的cullin家族成员,可以各自组装Cullin-RING E3连接酶复合物(CRL)并参与多种生物学过程。尽管由两个cullin成员形成的CRL可能具有共同的靶标,但是当在哺乳动物中发生突变或破坏时,两者似乎具有非常不同的后果。我们在这里通过使用吗啉代击倒方法研究了cul4a和cul4b在斑马鱼胚胎发生过程中的作用。我们发现cul4a对于心脏发育以及胸鳍发育至关重要。尽管cul4a morphant在腔室规格上似乎没有受到干扰,但它们并未经历心脏循环。 cul4a morphant中心脏循环和胸鳍形成的失败伴随着心脏细胞和胸鳍形成细胞的增殖大大降低。我们证明了tbx5a是心脏和四肢发育必不可少的转录因子,被cul4a转录上调并介导cul4a在心脏和胸鳍发育中的功能。与cul4a的至关重要性相反,cul4b似乎对斑马鱼的发育不可或缺,并且无法补偿cul4a的损失。这项工作首次证明了cul4a(而非cul4b)在斑马鱼的心脏发育和tbx5a调控中的重要作用。这些发现证明了探索CUL4A在人类心脏发育中的功能作用的合理性。

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