Skip Navigation

This Article
Right arrow Print PDF (1049K)
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 arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Mayeda, A.
Right arrow Articles by Ohshima, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mayeda, A.
Right arrow Articles by Ohshima, Y.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1990, Vol. 18, No. 16 4671-4676
© 1990


Articles

ß-globin transcripts carrying a single intron with three adjacent nucleotides of 5' exon are efficiently spliced in vitro irrespective of intron position or surrounding exon sequences

Akila Mayeda+ and Yasumi Ohshima*

Department of Biology, Faculty of Science, Kyushu University Hakozaki, Higashi-ku, Fukuoka 812, Japan

*To whom correspondence should be addressed

Received June 26, 1990. Accepted July 17, 1990.

To examine the role of exon sequences and intron position in the splicing of an mRNA precursor, we prepared series of sense or anti-sense transcripts of human ß-globin cDNA in which a cassette containing the ß-globin first intron was inserted into one of seven unusual positions. The intron cassette consisted of the intron alone (MI), the intron with three adjacent base pairs of the 5' exon (MI), or the intron with both 5' and 3' exon sequences. All these transcripts were examined in an in vitro splicing system with a HeLa cell nuclear extract. The sense transcripts carrying MI cassette were spliced efficiently and independently of the intron position, except when the 3' exon was too short. The anti-sense transcripts carrying MI cassette produced significantly less spliced products than did those of the sense transcripts. This was mostly because of the instability of the anti-sense transcripts, and the actual splicing efficiency was similar to that seen in the sense transcripts. Sense or anti-sense transcripts carrying MI cassette were spliced to various extents depending on the surrounding sequences. The results indicate that only three nucleotides of the 5' exon are required as specific exon sequences in the splicing of an mRNA precursor carrying a single intron, and that the intron position does not significantly affect the splicing efficiency in vitro.


+Present address: Cold Spring Harbor Laboratory, PO Box 100, Cold Spring Harbor, NY 11724, USA


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
GENES CELLSHome page
K. Masuyama, I. Taniguchi, N. Kataoka, and M. Ohno
SR proteins preferentially associate with mRNAs in the nucleus and facilitate their export to the cytoplasm
Genes Cells, October 1, 2004; 9(10): 959 - 965.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
K. Masuyama, I. Taniguchi, N. Kataoka, and M. Ohno
RNA length defines RNA export pathway
Genes & Dev., September 1, 2004; 18(17): 2074 - 2085.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
I. C. Eperon, O. V. Makarova, A. Mayeda, S. H. Munroe, J. F. Cáceres, D. G. Hayward, and A. R. Krainer
Selection of Alternative 5' Splice Sites: Role of U1 snRNP and Models for the Antagonistic Effects of SF2/ASF and hnRNP A1
Mol. Cell. Biol., November 15, 2000; 20(22): 8303 - 8318.
[Abstract] [Full Text]


Home page
Hum Mol GenetHome page
J.P. Venables, D.J. Elliott, O.V. Makarova, E.M. Makarov, H.J. Cooke, and I.C. Eperon
RBMY, a probable human spermatogenesis factor, and other hnRNP G proteins interact with Tra2{beta} and affect splicing
Hum. Mol. Genet., March 22, 2000; 9(5): 685 - 694.
[Abstract] [Full Text] [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.