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

机译:假定的长非编码RNA编码的微肽调节肌肉性能。

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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.
机译:功能性微肽可以隐藏在看起来非编码的RNA中。我们发现了一个保守的微肽,我们命名为Myoregulin(MLN),由骨骼肌特异性RNA编码,并被推定为长的非编码RNA。 MLN与phosphorlamban(PLN)和sarcolipin(SLN)具有结构和功能上的相似性,后者可抑制SERCA,SERCA是一种膜泵,通过调节Ca2 +对肌浆网(SR)的吸收来控制肌肉松弛。 MLN与SERCA直接相互作用,阻止Ca2 +吸收进入SR。与PLN和SLN在小鼠的心肌和慢速骨骼肌中表达相反,MLN在所有骨骼肌中均强烈表达。小鼠MLN的基因缺失可增强骨骼肌中的Ca2 +处理并改善运动表现。这些发现将MLN鉴定为骨骼肌生理的重要调节剂,并强调了在目前标注为非编码的许多RNA中编码其他微肽的可能性。

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