Skip Navigation

This Article
Right arrow Print PDF (2154K)
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 Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (26)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Iibri, D.
Right arrow Articles by Fiszman, M. Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Iibri, D.
Right arrow Articles by Fiszman, M. Y.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1989, Vol. 17, No. 16 6449-6462
© 1989


MOLECULAR BIOLOGY

A subfragment of the ß tropomyosin gene is alternatively spliced when transfected into differentiating muscle cells

Domenico Iibri, Joelle Marie1, Edward Brody1 and Marc Y. Fiszman*

Molecular Biology Department, Pasteur Institute Paris 1C.G.M., Batiment 24.CNRS, Gif sur Yvette France

*To whom correspondence should be addressed

Received June 29, 1989. Accepted July 19, 1989.

A subgenorruc fragment of the chicken ß tropomyosin gene which contains two alternative exons flanked by common exons was isolated and placed under the control of the SV 40 early promoter. This construction was subsequently used to transfect quail myoblasts together with a Neomycin resistance gene, and to isolate stable transfectants. mRNAs were isolated before and after differentiation and analyzed using a modification of the primer extension method. We show that myoblasts accumulate transcripts which contain the non muscle specific exon joined to the common exons while myotubes accumulate transcripts containing the muscle specific exon. These results, therefore demonstrate that such a subgenomic fragment contains all the necessary information to direct a correct developmentally regulated mutually exclusive splicing. They also strongly suggest that trans acting factors must be involved in the switch of the splicing pattern which takes place during the transition from myoblasts to myotubes. The same regulation cannot be faithfully reproduced during transient expression, since no difference in the use of exons 6A/6B is observed during differentiation and two aberrant minor splicing products are obtained which contain or lack both exons. We suggest that failure of exon 6A to splice to exon 6B is due to the existence of some structural constraints which lower the efficiency with which the intron between them is excised.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Physiol. Rev.Home page
P. Gunning, G. O'neill, and E. Hardeman
Tropomyosin-Based Regulation of the Actin Cytoskeleton in Time and Space
Physiol Rev, January 1, 2008; 88(1): 1 - 35.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A.-M. Pret and M. Y. Fiszman
Sequence Divergence Associated with Species-specific Splicing of the Nonmuscle beta-Tropomyosin Alternative Exon
J. Biol. Chem., May 10, 1996; 271(19): 11511 - 11517.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
B Clouet d'Orval, Y d'Aubenton Carafa, P Sirand-Pugnet, M Gallego, E Brody, and J Marie
RNA secondary structure repression of a muscle-specific exon in HeLa cell nuclear extracts
Science, June 28, 1991; 252(5014): 1823 - 1828.
[Abstract] [PDF]


Home page
ScienceHome page
D Libri, A Piseri, and M. Fiszman
Tissue-specific splicing in vivo of the beta-tropomyosin gene: dependence on an RNA secondary structure
Science, June 28, 1991; 252(5014): 1842 - 1845.
[Abstract] [PDF]


Home page
Genes Dev.Home page
M P Mullen, C W Smith, J G Patton, and B Nadal-Ginard
Alpha-tropomyosin mutually exclusive exon selection: competition between branchpoint/polypyrimidine tracts determines default exon choice.
Genes & Dev., April 1, 1991; 5(4): 642 - 655.
[Abstract] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.