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 PMID:25640239  

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

Douglas M Anderson | Kelly M Anderson | Chi-Lun Chang | Catherine A Makarewich | Benjamin R Nelson | John R McAnally | Prasad Kasaragod | John M Shelton | Jen Liou | Rhonda Bassel-Duby | Eric N Olson
Cell | 2015

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.

Pubmed ID: 25640239

Research resources used in this publication

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Associated grants

  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL077439
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK099653
  • Agency: NIDDK NIH HHS, United States
    Id: DK-099653
  • Agency: NHLBI NIH HHS, United States
    Id: U01 HL100401
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL053351
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL111665
  • Agency: NHLBI NIH HHS, United States
    Id: HL-077439
  • Agency: NHLBI NIH HHS, United States
    Id: U01-HL-100401
  • Agency: NHLBI NIH HHS, United States
    Id: HL-111665
  • Agency: NHLBI NIH HHS, United States
    Id: HL-093039
  • Agency: NIAMS NIH HHS, United States
    Id: 1F30AR067094-01
  • Agency: NIAMS NIH HHS, United States
    Id: F30 AR067094
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL093039

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ClusPro (tool)

RRID:SCR_018248

Web tool for protein-protein docking. Server provides removal of unstructured protein regions, application of attraction or repulsion, accounting for pairwise distance restraints, construction of homo-multimers, consideration of small-angle X-ray scattering data, and location of heparin-binding sites. Six different energy functions can be used, depending on protein type.This protocol describes use of various options, construction of auxiliary restraints files, selection of energy parameters, and analysis of results.

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