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非编码RNA在心脏发育和疾病中对基因调控程序的控制作用

Non-coding RNA in control of gene regulatory programs in cardiac development and disease.

作者信息

Philippen Leonne E, Dirkx Ellen, da Costa-Martins Paula A, De Windt Leon J

机构信息

Department of Cardiology, CARIM School for Cardiovascular Diseases, Maastricht University, 6229 ER Maastricht, The Netherlands.

Department of Cardiology, CARIM School for Cardiovascular Diseases, Maastricht University, 6229 ER Maastricht, The Netherlands; Department of Molecular Medicine, International Centre of Engineering and Biotechnology (ICGEB), 34149 Trieste, Italy.

出版信息

J Mol Cell Cardiol. 2015 Dec;89(Pt A):51-8. doi: 10.1016/j.yjmcc.2015.03.014. Epub 2015 Mar 27.

Abstract

Organogenesis of the vertebrate heart is a highly specialized process involving progressive specification and differentiation of distinct embryonic cardiac progenitor cell populations driven by specialized gene programming events. Likewise, the onset of pathologies in the adult heart, including cardiac hypertrophy, involves the reactivation of embryonic gene programs. In both cases, these intricate genomic events are temporally and spatially regulated by complex signaling networks and gene regulatory networks. Apart from well-established transcriptional mechanisms, increasing evidence indicates that gene programming in both the developing and the diseased myocardium are under epigenetic control by non-coding RNAs (ncRNAs). MicroRNAs regulate gene expression at the post-transcriptional level, and numerous studies have now established critical roles for this species of tiny RNAs in a broad range of aspects from cardiogenesis towards adult heart failure. Recent reports now also implicate the larger family of long non-coding RNAs (lncRNAs) in these processes as well. Here we discuss the involvement of these two ncRNA classes in proper cardiac development and hypertrophic disease processes of the adult myocardium. This article is part of a Special Issue entitled: Non-coding RNAs.

摘要

脊椎动物心脏的器官发生是一个高度专业化的过程,涉及由特殊基因编程事件驱动的不同胚胎心脏祖细胞群体的逐步特化和分化。同样,成年心脏疾病的发生,包括心脏肥大,涉及胚胎基因程序的重新激活。在这两种情况下,这些复杂的基因组事件在时间和空间上都受到复杂信号网络和基因调控网络的调节。除了已确立的转录机制外,越来越多的证据表明,发育中和患病心肌中的基因编程都受到非编码RNA(ncRNA)的表观遗传控制。微小RNA在转录后水平调节基因表达,现在许多研究已经证实了这种微小RNA在从心脏发生到成人心力衰竭的广泛方面的关键作用。最近的报道还表明,更大的长链非编码RNA(lncRNA)家族也参与了这些过程。在这里,我们讨论这两类ncRNA在成年心肌正常心脏发育和肥厚性疾病过程中的作用。本文是名为:非编码RNA的特刊的一部分。

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