A Micropeptide Encoded by a Putative Long Noncoding RNA Regulates Muscle Performance

被引:1306
作者
Anderson, Douglas M. [1 ,4 ]
Anderson, Kelly M. [1 ,4 ]
Chang, Chi-Lun [2 ]
Makarewich, Catherine A. [1 ,4 ]
Nelson, Benjamin R. [1 ,4 ]
McAnally, John R. [1 ,4 ]
Kasaragod, Prasad [1 ]
Shelton, John M. [3 ]
Liou, Jen [2 ]
Bassel-Duby, Rhonda [1 ,4 ]
Olson, Eric N. [1 ,4 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
[4] Univ Texas SW Med Ctr Dallas, Hamon Ctr Regenerat Sci & Med, Dallas, TX 75390 USA
关键词
RETICULUM CA2+ ATPASE; SKELETAL-MUSCLE; SARCOPLASMIC-RETICULUM; PHOSPHOLAMBAN ABLATION; CARDIAC CONTRACTILITY; PROTEIN EXPRESSION; HEART-FAILURE; MESSENGER-RNA; CALCIUM-PUMP; SARCOLIPIN;
D O I
10.1016/j.cell.2015.01.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Functional micropeptides can be concealed within RNAs that appear to be noncoding. We discovered a conserved micropeptide, which we named myoregulin (MLN), encoded by a skeletal muscle-specific RNA annotated as a putative long noncoding RNA. MLN shares structural and functional similarity with phospholamban (PLN) and sarcolipin (SLN), which inhibit SERCA, the membrane pump that controls muscle relaxation by regulating Ca2+ uptake into the sarcoplasmic reticulum (SR). MLN interacts directly with SERCA and impedes Ca2+ uptake into the SR. In contrast to PLN and SLN, which are expressed in cardiac and slow skeletal muscle in mice, MLN is robustly expressed in all skeletal muscle. Genetic deletion of MLN in mice enhances Ca2+ handling in skeletal muscle and improves exercise performance. These findings identify MLN as an important regulator of skeletal muscle physiology and highlight the possibility that additional micropeptides are encoded in the many RNAs currently annotated as noncoding.
引用
收藏
页码:595 / 606
页数:12
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