Literature DB >> 26160440

Role of microRNA-101a in the regulation of goat skeletal muscle satellite cell proliferation and differentiation.

Dandan Li1, Siyuan Zhan1, Yilin Wang1, Linjie Wang1, Tao Zhong1, Li Li1, Jingsheng Fan2, Chaorui Xiong2, Yong Wang3, Hongping Zhang4.   

Abstract

MicroRNAs are a class of small, non-coding RNAs that participate in the regulation of diverse biological processes including skeletal muscle development. However, the underlying molecular mechanisms are not fully understood, particularly in goat. Here, we identified goat miR-101a as a novel myogenic microRNA mediating myogenic differentiation. The expression of miR-101a was enriched in goat skeletal muscles and up-regulated during satellite cell differentiation. After transfection with a miR-101a mimic and culturing in differentiation medium, satellite cell differentiation was promoted, accompanied by a significant increase in mRNA expression of the myogenic marker, MyoG, and decreased expression of MyoD. In contrast, blocking the function of miR-101a with a 2'-O-methylated antisense oligonucleotide inhibitor repressed satellite cell differentiation. However, both gain- and loss-of-function studies demonstrated that miR-101a had no significant influence on satellite cell proliferation. Therefore, our results provide a new insight on miR-101a in the regulation of goat skeletal muscle satellite cell proliferation and differentiation.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Goat; MicroRNA; Myoblast differentiation; Myogenesis; miR-101a

Mesh:

Substances:

Year:  2015        PMID: 26160440     DOI: 10.1016/j.gene.2015.07.010

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  12 in total

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Journal:  Sci Rep       Date:  2017-03-24       Impact factor: 4.379

7.  A Novel Long Noncoding RNA, lncR-125b, Promotes the Differentiation of Goat Skeletal Muscle Satellite Cells by Sponging miR-125b.

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10.  The inhibition of miR‑101a‑3p alleviates H/R injury in H9C2 cells by regulating the JAK2/STAT3 pathway.

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Journal:  Mol Med Rep       Date:  2019-11-05       Impact factor: 2.952

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