Identification of long noncoding RNAs involved in muscle differentiation

被引:26
作者
Lim, Yeong-Hwan [1 ,2 ,3 ]
Kwon, Duk-Hwa [1 ,4 ]
Kim, Jaetaek [1 ,5 ]
Park, Woo Jin [1 ,6 ]
Kook, Hyun [1 ,3 ,4 ]
Kim, Young-Kook [1 ,2 ,3 ]
机构
[1] Chonnam Natl Univ, Med Sch, Basic Res Lab Cardiac Remodeling Res Lab, Jeollanam Do, South Korea
[2] Chonnam Natl Univ, Med Sch, Dept Biochem, Jeollanam Do, South Korea
[3] Chonnam Natl Univ, Ctr Creat Biomed Scientists, Dept Biomed Sci, Jeollanam Do, South Korea
[4] Chonnam Natl Univ, Med Sch, Dept Pharmacol, Jeollanam Do, South Korea
[5] Chung Ang Univ, Coll Med, Dept Internal Med, Div Endocrinol & Metab, Seoul, South Korea
[6] GIST, Coll Life Sci, Gwangju, South Korea
来源
PLOS ONE | 2018年 / 13卷 / 03期
基金
新加坡国家研究基金会;
关键词
VASCULAR SMOOTH-MUSCLE; CELLS IN-VITRO; STEM-CELLS; PHENOTYPIC MODULATION; RESPONSE FACTOR; HUMAN GENOME; VIVO; PROLIFERATION; HOMEOSTASIS; EXPRESSION;
D O I
10.1371/journal.pone.0193898
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 lnc RNAs. 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.
引用
收藏
页数:15
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