GTC
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE ADVANCED SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


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 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
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Smeets, M.
Right arrow Articles by Baldacci, G
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Smeets, M.
Right arrow Articles by Baldacci, G
GENES CELLS (2003) 8, 573-586.
Copyright © 2003 Blackwell Publishing or its licensors



Original Article

High dosage Rhp51 suppression of the MMS sensitivity of DNA structure checkpoint mutants reveals a relationship between Crb2 and Rhp51

MF Smeets, S Francesconi, and G Baldacci

BACKGROUND: In eukaryotic cells DNA structure checkpoints organize the cellular responses of DNA repair and transient cell cycle arrest and thereby ensure genomic stability. To investigate the exact role of crb2+ in the DNA damage checkpoint response, a genetic screen was carried out in order to identify suppressors of the conditional MMS sensitivity of a crb2-1 mutant. Here we report the isolation of rhp51+ as a multicopy suppressor. RESULTS: We show that suppression is not specific for the checkpoint mutant while it is specific for the MMS treatment. Rescue by rhp51+ over-expression is not a consequence of increased recombination repair or checkpoint compensation and epistasis analysis confirms that crb2+ and rhp51+ function in different pathways. A tight linkage between the two pathways is nevertheless suggested by the complementary expression or modification of Crb2 and Rhp51 proteins. Crb2 protein stability is down-regulated when Rhp51 is over-expressed and up-regulated in the absence of Rhp51. The up-regulation of Crb2 is independent of the activation of DNA structure checkpoints. Conversely Rhp51 is more readily activated and differentially modified in the absence of Crb2 or other checkpoint proteins. CONCLUSIONS: We conclude that fission yeast Crb2 and Rhp51 function in two parallel, tightly connected and coordinately regulated pathways.


This article has been cited by other articles:


Home page
GeneticsHome page
D. M. Sheedy, D. Dimitrova, J. K. Rankin, K. L. Bass, K. M. Lee, C. Tapia-Alveal, S. H. Harvey, J. M. Murray, and M. J. O'Connell
Brc1-Mediated DNA Repair and Damage Tolerance
Genetics, October 1, 2005; 171(2): 457 - 468.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
A. Collura, J. Blaisonneau, G. Baldacci, and S. Francesconi
The Fission Yeast Crb2/Chk1 Pathway Coordinates the DNA Damage and Spindle Checkpoint in Response to Replication Stress Induced by Topoisomerase I Inhibitor
Mol. Cell. Biol., September 1, 2005; 25(17): 7889 - 7899.
[Abstract] [Full Text] [PDF]


Home page
JCBHome page
P. Meister, A. Taddei, L. Vernis, M. Poidevin, S. M. Gasser, and G. Baldacci
Temporal separation of replication and recombination requires the intra-S checkpoint
J. Cell Biol., February 14, 2005; 168(4): 537 - 544.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
P. Meister, M. Poidevin, S. Francesconi, I. Tratner, P. Zarzov, and G. Baldacci
Nuclear factories for signalling and repairing DNA double strand breaks in living fission yeast
Nucleic Acids Res., September 1, 2003; 31(17): 5064 - 5073.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE ADVANCED SEARCH TABLE OF CONTENTS
Copyright © 2003 by Wiley-Blackwell Publishing.