心脏发育中的RNA结合蛋白。
RNA-binding proteins in heart development.
作者信息
Giudice Jimena, Cooper Thomas A
机构信息
Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX, 77030, USA,
出版信息
Adv Exp Med Biol. 2014;825:389-429. doi: 10.1007/978-1-4939-1221-6_11.
RNA-binding proteins (RBPs) are key players of posttranscriptional regulation occurring during normal tissue development. All tissues examined thus far have revealed the importance of RBPs in the regulation of complex networks involved in organ morphogenesis, maturation, and function. They are responsible for controlling tissue-specific gene expression by regulating alternative splicing, mRNA stability, translation, and poly-adenylation. The heart is the first organ form during embryonic development and is also the first to acquire functionality. Numerous remodeling processes take place during late cardiac development since fetal heart first adapts to birth and then undergoes a transition to adult functionality. This physiological remodeling involves transcriptional and posttranscriptional networks that are regulated by RBPs. Disruption of the normal regulatory networks has been shown to cause cardiomyopathy in humans and animal models. Here we review the complexity of late heart development and the current information regarding how RBPs control aspects of postnatal heart development. We also review how activities of RBPs are modulated adding complexity to the regulation of developmental networks.
RNA结合蛋白(RBPs)是正常组织发育过程中转录后调控的关键参与者。迄今为止,所有检测过的组织都揭示了RBPs在调控参与器官形态发生、成熟和功能的复杂网络中的重要性。它们通过调节可变剪接、mRNA稳定性、翻译和多聚腺苷酸化来控制组织特异性基因表达。心脏是胚胎发育过程中形成的第一个器官,也是第一个获得功能的器官。在心脏发育后期会发生许多重塑过程,因为胎儿心脏首先要适应出生,然后经历向成体功能的转变。这种生理重塑涉及由RBPs调控的转录和转录后网络。在人类和动物模型中,正常调控网络的破坏已被证明会导致心肌病。在这里,我们综述了心脏发育后期的复杂性以及关于RBPs如何控制出生后心脏发育方面的当前信息。我们还综述了RBPs的活性是如何被调节的,这增加了发育网络调控的复杂性。