Effect of miR-143-3p on C2C12 myoblast differentiation

被引:17
作者
Du, Jingjing [1 ]
Zhang, Yi [2 ]
Shen, Linyuan [1 ]
Luo, Jia [1 ]
Lei, Huaigang [3 ]
Zhang, Peiwen [1 ]
Pu, Qiang [1 ,4 ]
Liu, Yihui [1 ]
Shuai, Surong [1 ]
Li, Qiang
Li, Xuewi [1 ]
Zhang, Shunhua [1 ]
Zhu, Li [1 ]
机构
[1] Sichuan Agr Univ, Coll Anim Sci & Technol, Chengdu, Peoples R China
[2] Xichang Coll, Dept Anim Sci, Xichang, Peoples R China
[3] Univ Alberta, Dept Agr Food & Nutrit Sci, Edmonton, AB, Canada
[4] Sichuan Prov Gen Stn Anim Husb, Sichuan Prov Agr Dept, Chengdu, Peoples R China
关键词
miR-143-3p; C2C12; myoblast differentiation; Wnt pathway; PARAXIAL MESODERM; CANCER CELLS; MUSCLE; PROLIFERATION; MICRORNAS; TRANSCRIPTS; EXPRESSION; MYOGENESIS; MUTATIONS; PROMOTES;
D O I
10.1080/09168451.2015.1123604
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs are a class of 18-22 nucleotide non-coding RNAs that modulate gene expression by associating with the 3 untranslated regions of mRNAs. A large number of microRNAs are involved in the regulation of myoblast differentiation, many of which remain undiscovered. In this study, we found that miR-143-3p was upregulated during C2C12 myoblast differentiation and over-expression of miR-143-3p significantly inhibited the relative expression levels of MyoD, MyoG, myf5, and MyHC genes, especially in the later stages of differentiation. In addition, miR-143-3p inhibited expression of genes involved in the endogenous Wnt signaling pathway during C2C12 myoblast differentiation, including Wnt5a, LRP5, Axin2, and -catenin. These results indicate that miR-143-3p represents a new myogenic differentiation-associated microRNA that can inhibit C2C12 myoblast differentiation, especially in the later stages of differentiation.
引用
收藏
页码:706 / 711
页数:6
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