Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow Print PDF (117K) Freely available
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 (19)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Weidenhammer, E.
Right arrow Articles by Woolford, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Weidenhammer, E.
Right arrow Articles by Woolford, J., Jr
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, Vol 24, Issue 6 1164-1170, Copyright © 1996 by Oxford University Press


ARTICLES

The PRP31 gene encodes a novel protein required for pre-mRNA splicing in Saccharomyces cerevisiae

EM Weidenhammer, M Singh, M Ruiz-Noriega and JL Woolford Jr
Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA 15213 USA.

The pre-mRNA splicing factor Prp31p was identified in a screen of temperature-sensitive yeast strains for those exhibiting a splicing defect upon shift to the non- permissive temperature. The wild-type PRP31 gene was cloned and shown to be essential for cell viability. The PRP31 gene is predicted to encode a 60 kDa polypeptide. No similarities with other known splicing factors or motifs indicative of protein- protein or RNA-protein interaction domains are discernible in the predicted amino acid sequence. A PRP31 allele bearing a triple repeat of the hemagglutinin epitope has been generated. The tagged protein is functional in vivo and a single polypeptide species of the predicted size was detected by Western analysis with proteins from yeast cell extracts. Functional Prp31p is required for the processing of pre-mRNA species both in vivo and in vitro, indicating that the protein is directly involved in the splicing pathway.
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
Plant CellHome page
R. Chen, X. Zhao, Z. Shao, Z. Wei, Y. Wang, L. Zhu, J. Zhao, M. Sun, R. He, and G. He
Rice UDP-Glucose Pyrophosphorylase1 Is Essential for Pollen Callose Deposition and Its Cosuppression Results in a New Type of Thermosensitive Genic Male Sterility
PLANT CELL, March 1, 2007; 19(3): 847 - 861.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
Q. Wang and B. C. Rymond
Rds3p Is Required for Stable U2 snRNP Recruitment to the Splicing Apparatus
Mol. Cell. Biol., October 15, 2003; 23(20): 7339 - 7349.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
N. A. Faustino and T. A. Cooper
Pre-mRNA splicing and human disease
Genes & Dev., February 15, 2003; 17(4): 419 - 437.
[Full Text] [PDF]


Home page
Hum Mol GenetHome page
E. C. Deery, E. N. Vithana, R. J. Newbold, V. A. Gallon, S. S. Bhattacharya, Martin. J. Warren, D. M. Hunt, and S. E. Wilkie
Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31
Hum. Mol. Genet., December 1, 2002; 11(25): 3209 - 3219.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
R. W. M. Sablowski and E. M. Meyerowitz
Temperature-Sensitive Splicing in the Floral Homeotic Mutant apetala3-1
PLANT CELL, September 1, 1998; 10(9): 1453 - 1464.
[Abstract] [Full Text]



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.