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一种由假定的长链非编码RNA编码的微小肽调节肌肉性能。

A micropeptide encoded by a putative long noncoding RNA regulates muscle performance.

作者信息

Anderson Douglas M, Anderson Kelly M, Chang Chi-Lun, Makarewich Catherine A, Nelson Benjamin R, McAnally John R, Kasaragod Prasad, Shelton John M, Liou Jen, Bassel-Duby Rhonda, Olson Eric N

机构信息

Department of Molecular Biology, The University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9148, USA; Hamon Center for Regenerative Science and Medicine, The University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9148, USA.

Department of Physiology, The University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9148, USA.

出版信息

Cell. 2015 Feb 12;160(4):595-606. doi: 10.1016/j.cell.2015.01.009. Epub 2015 Jan 29.

Abstract

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 Ca(2+) uptake into the sarcoplasmic reticulum (SR). MLN interacts directly with SERCA and impedes Ca(2+) 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 Ca(2+) 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.

摘要

功能性微肽可能隐藏在看似非编码的RNA中。我们发现了一种保守的微肽,将其命名为肌调节素(MLN),它由一种骨骼肌特异性RNA编码,该RNA被注释为假定的长链非编码RNA。MLN与受磷蛋白(PLN)和肌浆素(SLN)在结构和功能上具有相似性,PLN和SLN可抑制肌浆网钙ATP酶(SERCA),SERCA是一种膜泵,通过调节钙离子摄取到肌浆网(SR)中来控制肌肉舒张。MLN直接与SERCA相互作用,并阻碍钙离子摄取到SR中。与在小鼠心脏和慢肌中表达的PLN和SLN不同,MLN在所有骨骼肌中均有强烈表达。小鼠中MLN的基因缺失增强了骨骼肌中的钙离子处理能力,并改善了运动表现。这些发现确定MLN是骨骼肌生理学的重要调节因子,并突出了在目前注释为非编码的许多RNA中编码其他微肽的可能性。

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