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Identification of long noncoding RNAs involved in muscle differentiation.
Lim, Yeong-Hwan; Kwon, Duk-Hwa; Kim, Jaetaek; Park, Woo Jin; Kook, Hyun; Kim, Young-Kook.
Affiliation
  • Lim YH; Basic Research Laboratory for Cardiac Remodeling Research Laboratory, Chonnam National University Medical School, Jeollanam-do, Republic of Korea.
  • Kwon DH; Department of Biochemistry, Chonnam National University Medical School, Jeollanam-do, Republic of Korea.
  • Kim J; Department of Biomedical Sciences, Center for Creative Biomedical Scientists at Chonnam National University, Jeollanam-do, Republic of Korea.
  • Park WJ; Basic Research Laboratory for Cardiac Remodeling Research Laboratory, Chonnam National University Medical School, Jeollanam-do, Republic of Korea.
  • Kook H; Department of Pharmacology, Chonnam National University Medical School, Jeollanam-do, Republic of Korea.
  • Kim YK; Basic Research Laboratory for Cardiac Remodeling Research Laboratory, Chonnam National University Medical School, Jeollanam-do, Republic of Korea.
PLoS One ; 13(3): e0193898, 2018.
Article in En | MEDLINE | ID: mdl-29499054
ABSTRACT
Long noncoding RNAs (lncRNAs) are a large class of regulatory RNAs with diverse roles in cellular processes. Thousands of lncRNAs have been discovered; however, their roles in the regulation of muscle differentiation are unclear because no comprehensive analysis of lncRNAs during this process has been performed. In the present study, by combining diverse RNA sequencing datasets obtained from public database, we discovered lncRNAs that could behave as regulators in the differentiation of smooth or skeletal muscle cells. These analyses confirmed the roles of previously reported lncRNAs in this process. Moreover, we discovered dozens of novel lncRNAs whose expression patterns suggested their possible involvement in the phenotypic switch of vascular smooth muscle cells. The comparison of lncRNA expression change suggested that many lncRNAs have common roles during the differentiation of smooth and skeletal muscles, while some lncRNAs may have opposite roles in this process. The expression change of lncRNAs was highly correlated with that of their neighboring genes, suggesting that they may function as cis-acting lncRNAs. Furthermore, within the lncRNA sequences, there were binding sites for miRNAs with expression levels inversely correlated with the expression of corresponding lncRNAs during differentiation, suggesting a possible role of these lncRNAs as competing endogenous RNAs. The lncRNAs identified in this study will be a useful resource for future studies of gene regulation during muscle differentiation.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Differentiation / Myocytes, Smooth Muscle / RNA, Long Noncoding Type of study: Diagnostic_studies Limits: Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2018 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Differentiation / Myocytes, Smooth Muscle / RNA, Long Noncoding Type of study: Diagnostic_studies Limits: Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2018 Document type: Article