Previous Article | Next Article 
Molecular and Cellular Biology, July 2006, p. 5406-5420, Vol. 26, No. 14
0270-7306/06/$08.00+0 doi:10.1128/MCB.00161-06
Copyright © 2006, American
Society for
Microbiology. All Rights Reserved.
Control of Translocations between Highly Diverged Genes by Sgs1, the Saccharomyces cerevisiae Homolog of the Bloom's Syndrome Protein
Kristina H. Schmidt,1,2*
Joann Wu,1 and
Richard D. Kolodner1
Ludwig Institute for Cancer Research, Departments of Medicine and Cellular and Molecular Medicine, and Cancer Center, University of California San Diego, School of Medicine, La Jolla, California 92093,1
Department of Biology, University of South Florida, 4202 E. Fowler Avenue, SCA110, Tampa, Florida
336202
Received 27 January 2006/
Returned for modification 24 February 2006/
Accepted 28 April 2006
Sgs1 is a RecQ family DNA helicase required for genome stability in
Saccharomyces cerevisiae whose human homologs BLM, WRN, and
RECQL4 are mutated in Bloom's, Werner, and Rothmund Thomson syndromes,
respectively. Sgs1 and mismatch repair (MMR) are inhibitors of
recombination between similar but divergent (homeologous) DNA
sequences. Here we show that SGS1, but not MMR, is critical
for suppressing spontaneous, recurring translocations between diverged
genes in cells with mutations in the genes encoding the checkpoint
proteins Mec3, Rad24, Rad9, or Rfc5, the chromatin assembly factors
Cac1 or Asf1, and the DNA helicase Rrm3. The S-phase checkpoint kinase
and telomere maintenance factor Tel1, a homolog of the human ataxia
telangiectasia (ATM) protein, prevents these translocations, whereas
the checkpoint kinase Mec1, a homolog of the human ATM-related protein,
and the Rad53 checkpoint kinase are not required. The translocation
structures observed suggest involvement of a dicentric intermediate and
break-induced replication with multiple cycles of DNA template
switching.
* Corresponding author. Mailing address: Department of Biology, University of South Florida, 4202 E. Fowler Avenue, SCA110, Tampa, FL 33620. Phone: (813) 974-1592. Fax: (813) 974-3263. E-mail:
kschmidt{at}cas.usf.edu.
Molecular and Cellular Biology, July 2006, p. 5406-5420, Vol. 26, No. 14
0270-7306/06/$08.00+0 doi:10.1128/MCB.00161-06
Copyright © 2006, American
Society for
Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Ruiz, J. F., Gomez-Gonzalez, B., Aguilera, A.
(2009). Chromosomal Translocations Caused by Either Pol32-Dependent or Pol32-Independent Triparental Break-Induced Replication. Mol. Cell. Biol.
29: 5441-5454
[Abstract]
[Full Text]
-
Smith, C. E., Lam, A. F., Symington, L. S.
(2009). Aberrant Double-Strand Break Repair Resulting in Half Crossovers in Mutants Defective for Rad51 or the DNA Polymerase {delta} Complex. Mol. Cell. Biol.
29: 1432-1441
[Abstract]
[Full Text]
-
Kappeler, M., Kranz, E., Woolcock, K., Georgiev, O., Schaffner, W.
(2008). Drosophila bloom helicase maintains genome integrity by inhibiting recombination between divergent DNA sequences. Nucleic Acids Res
36: 6907-6917
[Abstract]
[Full Text]
-
Lee, J. Y., Mogen, J. L., Chavez, A., Johnson, F. B.
(2008). Sgs1 RecQ Helicase Inhibits Survival of Saccharomyces cerevisiae Cells Lacking Telomerase and Homologous Recombination. J. Biol. Chem.
283: 29847-29858
[Abstract]
[Full Text]
-
Banerjee, S., Smith, S., Oum, J.-H., Liaw, H.-J., Hwang, J.-Y., Sikdar, N., Motegi, A., Lee, S. E., Myung, K.
(2008). Mph1p promotes gross chromosomal rearrangement through partial inhibition of homologous recombination. JCB
181: 1083-1093
[Abstract]
[Full Text]
-
Deem, A., Barker, K., VanHulle, K., Downing, B., Vayl, A., Malkova, A.
(2008). Defective Break-Induced Replication Leads to Half-Crossovers in Saccharomyces cerevisiae. Genetics
179: 1845-1860
[Abstract]
[Full Text]
-
Nolan, T., Cecere, G., Mancone, C., Alonzi, T., Tripodi, M., Catalanotto, C., Cogoni, C.
(2008). The RNA-dependent RNA polymerase essential for post-transcriptional gene silencing in Neurospora crassa interacts with replication protein A. Nucleic Acids Res
36: 532-538
[Abstract]
[Full Text]
-
Tripathi, V., Nagarjuna, T., Sengupta, S.
(2007). BLM helicase dependent and independent roles of 53BP1 during replication stress mediated homologous recombination. JCB
178: 9-14
[Abstract]
[Full Text]
-
Schmidt, K. H., Kolodner, R. D.
(2006). Suppression of spontaneous genome rearrangements in yeast DNA helicase mutants. Proc. Natl. Acad. Sci. USA
103: 18196-18201
[Abstract]
[Full Text]