Han Lei, Yang Lei
Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, United States.
Front Cardiovasc Med. 2021 Sep 16;8:728746. doi: 10.3389/fcvm.2021.728746. eCollection 2021.
With the large-scale genome-wide sequencing, long non-coding RNAs (lncRNAs) have been found to compose of a large portion of the human transcriptome. Recent studies demonstrated the multidimensional functions of lncRNAs in heart development and disease. The subcellular localization of lncRNA is considered as a key factor that determines lncRNA function. Cytosolic lncRNAs mainly regulate mRNA stability, mRNA translation, miRNA processing and function, whereas nuclear lncRNAs epigenetically regulate chromatin remodeling, structure, and gene transcription. In this review, we summarize the molecular mechanisms of cytosolic and nuclear lncRNAs in heart development and disease separately, and emphasize the recent progress to dictate the crosstalk of cytosolic and nuclear lncRNAs in orchestrating the same biological process. Given the low evolutionary conservation of most lncRNAs, deeper understanding of human lncRNA will uncover a new layer of human regulatory mechanism underlying heart development and disease, and benefit the future clinical treatment for human heart disease.
随着大规模全基因组测序技术的发展,人们发现长链非编码RNA(lncRNA)构成了人类转录组的很大一部分。最近的研究表明lncRNA在心脏发育和疾病中具有多维度功能。lncRNA的亚细胞定位被认为是决定其功能的关键因素。胞质lncRNA主要调节mRNA稳定性、mRNA翻译、miRNA加工及功能,而核lncRNA则通过表观遗传调控染色质重塑、结构及基因转录。在本综述中,我们分别总结了胞质和核lncRNA在心脏发育和疾病中的分子机制,并着重阐述了近期在揭示胞质和核lncRNA在协调同一生物学过程中的相互作用方面取得的进展。鉴于大多数lncRNA的进化保守性较低,对人类lncRNA的深入理解将揭示心脏发育和疾病背后人类调控机制的新层面,并造福于未来人类心脏病的临床治疗。