MicroRNA-27a inhibits porcine type I muscle fibre gene expression by directly targeting peroxisome proliferator-activated receptor-γ coactivator-1α

被引:3
作者
Wang, Weiwei [1 ]
Yu, Qinping [1 ]
Cao, Qingyun [1 ]
Ye, Hui [1 ]
Zhang, Changming [1 ]
Dong, Zemin [1 ]
Feng, Dingyuan [1 ]
Zuo, Jianjun [1 ,2 ]
机构
[1] South China Agr Univ, Coll Anim Sci, Guangdong Prov Key Lab Anim Nutr Control, Guangzhou, Peoples R China
[2] South China Agr Univ, Coll Anim Sci, Guangdong Prov Key Lab Anim Nutr Control, Guangzhou 510642, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-27a; myosin heavy chain; PGC-1; alpha; pig; signalling pathway; type I muscle fibre; MITOCHONDRIAL TRANSCRIPTION FACTOR; CYTOCHROME-C-OXIDASE; SKELETAL-MUSCLE; NUCLEAR; OVEREXPRESSION; RECOGNITION; CONVERSION; PCR;
D O I
10.1111/jpn.13822
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
MicroRNAs are one of the key determinants of muscle fibre development and phenotype in mammals. The preliminary experiment implied that microRNA-27a (miR-27a) might involve in regulation of muscle fibre type composition of pigs. Thereby, the present study aimed to confirm the regulatory effect of miR-27a on porcine type I muscle fibre-encoding gene (myosin heavy chain gene 7, MYH7) expression and its related mechanism. We firstly observed opposite expression patterns between miR-27a and MYH7 as well as between miR-27a and peroxisome proliferator-activated receptor-? coactivator-1a (PGC-1a) during differentiation of porcine skeletal muscle satellite cells. Through the subsequent transfection analysis in porcine myotubes, we found that miR-27a suppressed the expression of MYH7 and PGC-1a. Besides, miR-27a induced inhibition of PGC-1a downstream targets, namely myocyte enhancer factor-2C (MEF2C) along with mitochondrial biogenesis and oxidative metabolism-related factors such as nuclear respiratory factor 1 (NRF-1), mitochondrial transcription factor A (mtTFA), cytochrome c (Cytc) and cytochrome oxidase IV (COX ?) and succinodehydrogenase (SDH). Dual-luciferase reporter analysis revealed that miR-27a could bind to the predicted target site in the 3MODIFIER LETTER PRIME-untranslated regions of PGC-1a mRNA, confirming a direct targeting of PGC-1a by miR-27a. Moreover, PGC-1a silencing abolished the promotive effects of miR-27a inhibitor on MYH7, PGC-1a and its downstream targets (MEF2C, NRF-1, mtTFA, COX ?, Cytc and SDH) in porcine myotubes. Collectively, miR-27a inhibits porcine MYH7 expression by negatively regulating PGC-1a and PGC-1a-controlled MEF2C expression as well as mitochondrial biogenesis and oxidative metabolism. Our findings may provide a molecular target for genetic or nutritional control of muscle fibre phenotype of pigs, probably having an important implication for regulating pork quality.
引用
收藏
页码:1054 / 1064
页数:11
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