A Family of microRNAs Encoded by Myosin Genes Governs Myosin Expression and Muscle Performance

被引:876
作者
van Rooij, Eva [1 ,3 ]
Quiat, Daniel [1 ]
Johnson, Brett A. [1 ]
Sutherland, Lillian B. [1 ]
Qi, Xiaoxia [1 ]
Richardson, James A. [1 ,2 ]
Kelm, Robert J., Jr. [4 ]
Olson, Eric N. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
[3] MiRagen Therapeut, Boulder, CO 80301 USA
[4] Univ Vermont, Coll Med, Dept Med, Burlington, VT 05405 USA
基金
美国国家卫生研究院;
关键词
HEAVY-CHAIN GENE; RAT SKELETAL-MUSCLE; CARDIAC-HYPERTROPHY; HEART-FAILURE; ALPHA-MYOSIN; FIBER-TYPE; ISOFORM EXPRESSION; POWER OUTPUT; PUR-ALPHA; PROTEINS;
D O I
10.1016/j.devcel.2009.10.013
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Myosin is the primary regulator of muscle strength and contractility. Here we show that three myosin genes, Myh6, Myh7, and Myh7b, encode related intronic microRNAs (miRNAs), which, in turn, control muscle myosin content, myofiber identity, and muscle performance. Within the adult heart, the Myh6 gene, encoding a fast myosin, coexpresses miR-208a, which regulates the expression of two slow myosins and their intronic miRNAs, Myh7/miR-208b and Myh7b/miR-499, respectively. miR-208b and miR-499 play redundant roles in the specification of muscle fiber identity by activating slow and repressing fast myofiber gene programs. The actions of these miRNAs are mediated in part by a collection of transcriptional repressors of slow myofiber genes. These findings reveal that myosin genes not only encode the major contractile proteins of muscle, but act more broadly to influence muscle function by encoding a network of intronic miRNAs that control muscle gene expression and performance.
引用
收藏
页码:662 / 673
页数:12
相关论文
共 48 条
[1]  
ADOLPH EA, 1993, J BIOL CHEM, V268, P5349
[2]   Sp3 inhibits Sp1-mediated activation of the cardiac troponin T promoter and is downregulated during pathological cardiac hypertrophy in vivo [J].
Azakie, Anthony ;
Fineman, Jeffrey R. ;
He, Youping .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2006, 291 (02) :H600-H611
[3]   The impact of microRNAs on protein output [J].
Baek, Daehyun ;
Villen, Judit ;
Shin, Chanseok ;
Camargo, Fernando D. ;
Gygi, Steven P. ;
Bartel, David P. .
NATURE, 2008, 455 (7209) :64-U38
[4]   Effects of different activity and inactivity paradigms on myosin heavy chain gene expression in striated muscle [J].
Baldwin, KM ;
Haddad, F .
JOURNAL OF APPLIED PHYSIOLOGY, 2001, 90 (01) :345-357
[5]   3 FAST MYOSIN HEAVY-CHAINS IN ADULT-RAT SKELETAL-MUSCLE [J].
BAR, A ;
PETTE, D .
FEBS LETTERS, 1988, 235 (1-2) :153-155
[6]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[7]   Signaling pathways in skeletal muscle remodeling [J].
Bassel-Duby, Rhonda ;
Olson, Eric N. .
ANNUAL REVIEW OF BIOCHEMISTRY, 2006, 75 :19-37
[8]   Diversity of microRNAs in human and chimpanzee brain [J].
Berezikov, Eugene ;
Thuemmler, Fritz ;
van Laake, Linda W. ;
Kondova, Ivanela ;
Bontrop, Ronald ;
Cuppen, Edwin ;
Plasterk, Ronald H. A. .
NATURE GENETICS, 2006, 38 (12) :1375-1377
[9]   MicroRNA-208a is a regulator of cardiac hypertrophy and conduction in mice [J].
Callis, Thomas E. ;
Pandya, Kumar ;
Seok, Hee Young ;
Tang, Ru-Hang ;
Tatsuguchi, Mariko ;
Huang, Zhan-Peng ;
Chen, Jian-Fu ;
Deng, Zhongliang ;
Gunn, Bronwyn ;
Shumate, Janelle ;
Willis, Monte S. ;
Selzman, Craig H. ;
Wang, Da-Zhi .
JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (09) :2772-2786
[10]   An abnormal Ca2+ response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy [J].
Fatkin, D ;
McConnell, BK ;
Mudd, JO ;
Semsarian, C ;
Moskowitz, IGP ;
Schoen, FJ ;
Giewat, M ;
Seidman, CE ;
Seidman, JG .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (11) :1351-1359