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鉴定 MyoD 反应性转录本揭示了一种新的长非编码 RNA(lncRNA-AK143003),其负调控成肌细胞分化。

Identification of MyoD-Responsive Transcripts Reveals a Novel Long Non-coding RNA (lncRNA-AK143003) that Negatively Regulates Myoblast Differentiation.

机构信息

Key Laboratory of Swine Genetics and Breeding of Ministry of Agriculture & Key Laboratory of Agriculture Animal Genetics, Breeding and Reproduction of Ministry of Education, College of Animal Science, Huazhong Agricultural University, Wuhan, 430070, Hubei, P.R. China.

National Key Laboratory of Crop Genetic Improvement, Agricultural Bioinformatics Key Laboratory of Hubei Province, College of Informatics, Huazhong Agricultural University, Wuhan, 430070, Hubei, P.R. China.

出版信息

Sci Rep. 2017 Jun 6;7(1):2828. doi: 10.1038/s41598-017-03071-7.

DOI:10.1038/s41598-017-03071-7
PMID:28588232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5460278/
Abstract

Myogenic differentiation factor (MyoD) is a master transcription factor in muscle development and differentiation. Although several long non-coding RNAs (lncRNAs) linked to MyoD have been found to influence muscle development, the functions of many lncRNAs have not been explored. Here we utilized lncRNA and mRNA microarray analysis to identify potential lncRNAs regulated by MyoD in muscle cells. A total of 997 differentially expressed lncRNAs (335 up-regulated and 662 down-regulated) and 1,817 differentially expressed mRNAs (148 up-regulated and 1,669 down-regulated) were identified after MyoD knockdown in C2C12 cells. Functional predictions suggested that most lncRNAs are involved in the biological pathways related to muscle differentiation and cell cycle with co-expressed genes. To gain further insight into the MyoD-mediated lncRNA expression in muscle differentiation, tissue expression profiles and MyoD overexpression were performed, and we found one of the candidate lncRNAs-AK143003 was significantly regulated by MyoD. Further analyses showed its noncoding ability and cytoplasmic localisation. Silencing of AK143003 stimulated the accumulation of myogenic marker genes, whereas AK143003 overexpression led to their decreased synthesis. This study identified a multitude of MyoD-mediated lncRNAs for further investigation and identified a novel lncRNA, lnc-AK143003, which plays a role in controlling muscle differentiation.

摘要

肌源性分化因子(MyoD)是肌肉发育和分化的主要转录因子。尽管已经发现了几种与 MyoD 相关的长非编码 RNA(lncRNA)影响肌肉发育,但许多 lncRNA 的功能尚未得到探索。在这里,我们利用 lncRNA 和 mRNA 微阵列分析来鉴定 MyoD 在肌肉细胞中调控的潜在 lncRNA。MyoD 敲低后,C2C12 细胞中共有 997 个差异表达的 lncRNA(335 个上调和 662 个下调)和 1817 个差异表达的 mRNA(148 个上调和 1669 个下调)被鉴定出来。功能预测表明,大多数 lncRNA 参与与肌肉分化和细胞周期相关的生物途径,与共表达基因有关。为了更深入地了解 MyoD 介导的肌肉分化中的 lncRNA 表达,我们进行了组织表达谱分析和 MyoD 过表达,发现候选 lncRNA 之一-AK143003 被 MyoD 显著调控。进一步的分析表明它具有非编码能力和细胞质定位。AK143003 的沉默刺激了肌生成标记基因的积累,而 AK143003 的过表达导致其合成减少。这项研究鉴定了大量由 MyoD 介导的 lncRNA 进行进一步研究,并鉴定了一个新的 lncRNA,lnc-AK143003,它在控制肌肉分化中发挥作用。

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