Am J Physiol Cell Physiol AJP: Lung Cellular and Molecular Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Cell Physiol 293: C451-C457, 2007. First published April 25, 2007; doi:10.1152/ajpcell.00077.2007
0363-6143/07 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
293/1/C451    most recent
00077.2007v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (9)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by McCarthy, J. J.
Right arrow Articles by Andrade, F. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by McCarthy, J. J.
Right arrow Articles by Andrade, F. H.

MUSCLE CELL BIOLOGY AND CELL MOTILITY

MicroRNA-206 is overexpressed in the diaphragm but not the hindlimb muscle of mdx mouse

John J. McCarthy, Karyn A. Esser, and Francisco H. Andrade

Department of Physiology, University of Kentucky Medical Center, Lexington, Kentucky

Submitted 22 February 2007 ; accepted in final form 18 April 2007

MicroRNAs are highly conserved, noncoding RNAs involved in posttranscriptional gene silencing. MicroRNAs have been shown to be involved in a range of biological processes, including myogenesis and muscle regeneration. The objective of this study was to test the hypothesis that microRNA expression is altered in dystrophic muscle, with the greatest change occurring, of the muscles examined, in the diaphragm. The expression of the muscle-enriched microRNAs was determined in the soleus, plantaris, and diaphragm muscles of control and dystrophin-deficient (mdx) mice by semiquantitative PCR. In the soleus and plantaris, expression of the mature microRNA 133a (miR-133a) and miR-206, respectively, was decreased by ~25%, whereas in the diaphragm, miR-206 expression increased by 4.5-fold relative to control. The increased expression of miR-206 in the mdx diaphragm was paralleled by a 4.4-fold increase in primary miRNA-206 (pri-miRNA-206) transcript level. Expression of Myod1 was elevated 2.7-fold only in the mdx diaphragm, consistent with an earlier finding demonstrating Myod1 can activate pri-miRNA-206 transcription. Transcript levels of Drosha and Dicer, major components of microRNA biogenesis pathway, were unchanged in mdx muscle, suggesting the pathway is not altered under dystrophic conditions. Previous in vitro analysis found miR-206 was capable of repressing utrophin expression; however, under dystrophic conditions, both utrophin transcript and protein levels were significantly increased by 69% and 3.9-fold, respectively, a finding inconsistent with microRNA regulation. These results are the first to report alterations in expression of muscle-enriched microRNAs in skeletal muscle of the mdx mouse, suggesting microRNAs may have a role in the pathophysiology of muscular dystrophy.

muscular dystrophy; posttranscriptional; gene regulation



Address for reprint requests and other correspondence: J. J. McCarthy, Dept. of Physiology, Univ. of Kentucky Medical Center, 800 Rose St., Lexington, KY 40536-0298 (e-mail: jjmcca2{at}uky.edu)




This article has been cited by other articles:


Home page
Physiol. GenomicsHome page
J. J. McCarthy, K. A. Esser, C. A. Peterson, and E. E. Dupont-Versteegden
Evidence of MyomiR network regulation of {beta}-myosin heavy chain gene expression during skeletal muscle atrophy
Physiol Genomics, November 1, 2009; 39(3): 219 - 226.
[Abstract] [Full Text] [PDF]


Home page
FASEB J.Home page
S. Greco, M. De Simone, C. Colussi, G. Zaccagnini, P. Fasanaro, M. Pescatori, R. Cardani, R. Perbellini, E. Isaia, P. Sale, et al.
Common micro-RNA signature in skeletal muscle damage and regeneration induced by Duchenne muscular dystrophy and acute ischemia
FASEB J, October 1, 2009; 23(10): 3335 - 3346.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
J.-F. Chen, T. E. Callis, and D.-Z. Wang
microRNAs and muscle disorders
J. Cell Sci., January 1, 2009; 122(1): 13 - 20.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
M. J. Drummond, J. J. McCarthy, C. S. Fry, K. A. Esser, and B. B. Rasmussen
Aging differentially affects human skeletal muscle microRNA expression at rest and after an anabolic stimulus of resistance exercise and essential amino acids
Am J Physiol Endocrinol Metab, December 1, 2008; 295(6): E1333 - E1340.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2007 by the American Physiological Society.