Open Access
Cell, volume 160, issue 4, pages 595-606
A Micropeptide Encoded by a Putative Long Noncoding RNA Regulates Muscle Performance
ANDERSON DOUGLAS M.
1
,
Anderson Kelly M
1
,
Chang Chi-Lun
2
,
Makarewich Catherine A.
1
,
Nelson Benjamin R
1
,
McAnally John
1
,
Kasaragod Prasad
3
,
John W. Shelton (2) John
4
,
Liou Jen
2
,
Bassel-Duby Rhonda
1
,
Olson Eric J.
1
1
Hamon Center for Regenerative Science and Medicine, The University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390–9148, USA
|
2
Department of Physiology, The University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9148, USA.
|
3
Department of Molecular Biology, The University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390–9148, USA
|
4
Department of Internal Medicine, The University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390–9148, USA
|
Publication type: Journal Article
Publication date: 2015-02-01
PubMed ID:
25640239
General Biochemistry, Genetics and Molecular Biology
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.
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- We do not take into account publications that without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
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ANDERSON D. M. et al. A Micropeptide Encoded by a Putative Long Noncoding RNA Regulates Muscle Performance // Cell. 2015. Vol. 160. No. 4. pp. 595-606.
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ANDERSON D. M., Anderson K. M., Chang C., Makarewich C. A., Nelson B. R., McAnally J., Kasaragod P., John W. Shelton (2) J., Liou J., Bassel-Duby R., Olson E. J. A Micropeptide Encoded by a Putative Long Noncoding RNA Regulates Muscle Performance // Cell. 2015. Vol. 160. No. 4. pp. 595-606.
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TY - JOUR
DO - 10.1016/j.cell.2015.01.009
UR - https://doi.org/10.1016%2Fj.cell.2015.01.009
TI - A Micropeptide Encoded by a Putative Long Noncoding RNA Regulates Muscle Performance
T2 - Cell
AU - ANDERSON, DOUGLAS M.
AU - Anderson, Kelly M
AU - Chang, Chi-Lun
AU - Makarewich, Catherine A.
AU - Nelson, Benjamin R
AU - McAnally, John
AU - Kasaragod, Prasad
AU - John W. Shelton (2), John
AU - Liou, Jen
AU - Bassel-Duby, Rhonda
AU - Olson, Eric J.
PY - 2015
DA - 2015/02/01 00:00:00
PB - Elsevier
SP - 595-606
IS - 4
VL - 160
PMID - 25640239
SN - 0092-8674
SN - 1097-4172
ER -
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@article{2015_ANDERSON,
author = {DOUGLAS M. ANDERSON and Kelly M Anderson and Chi-Lun Chang and Catherine A. Makarewich and Benjamin R Nelson and John McAnally and Prasad Kasaragod and John John W. Shelton (2) and Jen Liou and Rhonda Bassel-Duby and Eric J. Olson},
title = {A Micropeptide Encoded by a Putative Long Noncoding RNA Regulates Muscle Performance},
journal = {Cell},
year = {2015},
volume = {160},
publisher = {Elsevier},
month = {feb},
url = {https://doi.org/10.1016%2Fj.cell.2015.01.009},
number = {4},
pages = {595--606},
doi = {10.1016/j.cell.2015.01.009}
}
Cite this
MLA
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ANDERSON, DOUGLAS M., et al. “A Micropeptide Encoded by a Putative Long Noncoding RNA Regulates Muscle Performance.” Cell, vol. 160, no. 4, Feb. 2015, pp. 595-606. https://doi.org/10.1016%2Fj.cell.2015.01.009.