spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kobiyama, A.
Right arrow Articles by Watabe, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kobiyama, A.
Right arrow Articles by Watabe, S.

Journal of Experimental Biology, Vol 201, Issue 20 2801-2813, Copyright © 1998 by Company of Biologists


JOURNAL ARTICLES

Molecular cloning and developmental expression patterns of the MyoD and MEF2 families of muscle transcription factors in the carp

A Kobiyama, Y Nihei, Y Hirayama, K Kikuchi, H Suetake, IA Johnston and S Watabe
Laboratory of Aquatic Molecular Biology and Biotechnology, Laboratory of Aquatic Animal Physiology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo, Tokyo 113-8657, Japan and Gatty Marine Laboratory, School of Environmental and Evolutionary Biology, University of St Andrews, St Andrews, Fife KY16 8LB, Scotland. awatabe@hongo.ecc.u-tokyo.ac.jp

cDNA clones encoding the myogenic regulatory factors (MRFs) myogenin, MyoD and myf-5 were isolated by reverse-transcription polymerase chain reaction from larvae and embryos of the common carp (Cyprinus carpio L.). Myocyte-specific enhancer factor 2 (MEF2) cDNAs were identified from a cDNA library from adult carp. Northern blot analysis showed that MyoD, myf-5 and MEF2C transcripts were present in three-somite embryos, whereas myogenin and MEF2A transcripts were not detected until the 15-somite stage. Intense signals of myogenin and MyoD transcripts were observed even in 1-month-old juveniles. Levels of MyoD, myogenin and MEF2A transcripts declined between 1 and 7 months after hatching, and myf-5 gave only a weak signal in the oldest fish. In contrast, levels of MEF2C transcripts were considerably higher in 7-month-old juveniles than in 1-month-old larvae. mRNAs encoding carp myosin heavy chain and -actin were first detected at approximately the time of the first heartbeat, and levels were maximal in juveniles 1 month post-hatching. The relatively high levels of MRF mRNA in juvenile fish probably reflect the recruitment of new muscle fibres from the satellite cell population. It was concluded that the relative importance of the different members of the MyoD and MEF2 families of transcription factors for muscle differentiation changes during ontogeny in the carp.


This article has been cited by other articles:


Home page
J. Exp. Biol.Home page
J. A. Kim, C. Laney, J. Curry, and G. A. Unguez
Expression of myogenic regulatory factors in the muscle-derived electric organ of Sternopygus macrurus
J. Exp. Biol., July 1, 2008; 211(13): 2172 - 2184.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
H.-Y. Le, Y. Zhang, H. Liu, L.-H. Ma, Y. Jin, Q.-H. Huang, Y. Chen, M. Deng, Z. Chen, S.-J. Chen, et al.
eena Promotes Myeloid Proliferation through Stimulating ERK1/2 Phosphorylation in Zebrafish
J. Biol. Chem., June 20, 2008; 283(25): 17652 - 17661.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 1998