Activation of a novel pathway involving Mms1 and Rad59 in sgs1 cells

Biochemical and Biophysical Research Communications

Volumn 356, Issue 4, 2007, Pages 1031-1037

  Ui, Ayako ^a   Seki, Masayuki ^a   Ogiwara, Hideaki ^a   Lai, Mong Sing ^a   Yamamoto, Kazuo ^a   Tada, Shusuke ^a   Enomoto, Takemi ^a  

^a TOHOKU UNIVERSITY   (Japan)

Author keywords

Bloom syndrome; Mms1; Mms22; Rad51; Recombination; RecQ; Rtt101; Rtt107; Rtt109; Template switch

Indexed keywords

NUCLEIC ACID BINDING PROTEIN; PROTEIN RAD1; PROTEIN RAD59; RAD51 PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BLOOM SYNDROME; CELL MUTANT; CONTROLLED STUDY; DNA DAMAGE; GENE ACTIVATION; GENETIC RECOMBINATION; MUTATION; NONHUMAN; PRIORITY JOURNAL; SISTER CHROMATID; YEAST;

DNA DAMAGE; DNA-BINDING PROTEINS; RAD52 DNA REPAIR AND RECOMBINATION PROTEIN; RECQ HELICASES; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; SIGNAL TRANSDUCTION; SISTER CHROMATID EXCHANGE;

SACCHAROMYCETALES;

EID: 34047094406     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2007.03.088     Document Type: Article

References (25)

1. Kuzminov A. DNA replication meets genetic exchange: chromosomal damage and its repair by homologous recombination. Proc. Natl. Acad. Sci. USA 98 (2001) 8461-8468
2. Kadyk L.C., and Hartwell L.H. Sister chromatids are preferred over homologs as substrates for recombinational repair in Saccharomyces cerevisiae. Genetics 132 (1992) 387-402
3. Kadyk L.C., and Hartwell L.H. Replication-dependent sister chromatid recombination in rad1 mutants of Saccharomyces cerevisiae. Genetics 133 (1993) 469-487
4. Paques F., and Haber J.E. Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae. Microbiol. Mol. Biol. Rev. 63 (1999) 349-404
5. Prado F., Cortes-Ledesma F., Huertas P., and Aguilera A. Mitotic recombination in Saccharomyces cerevisiae. Curr. Genet. 42 (2003) 185-198
6. Pan X., Ye P., Yuan D.S., Wang X., Bader J.S., and Boeke J.D. A DNA integrity network in the yeast Saccharomyces cerevisiae. Cell 124 (2006) 1069-1081
7. Hryciw T., Tang M., Fontanie T., and Xiao W. MMS1 protects against replication-dependent DNA damage in Saccharomyces cerevisiae. Mol. Genet. Genomics 266 (2002) 848-857
8. Araki Y., Kawasaki Y., Sasanuma H., Tye B.K., and Sugino A. Budding yeast mcm10/dna43 mutant requires a novel repair pathway for viability. Genes Cells 8 (2003) 465-480
9. Driscoll R., Hudson A., and Jackson S.P. Yeast Rtt109 promotes genome stability by acetylating histone H3 on lysine 56. Science 315 (2007) 649-652
10. Han J., Zhou H., Horazdovsky B., Zhang K., Xu R.M., and Zhang Z. Rtt109 acetylates histone H3 lysine 56 and functions in DNA replication. Science 315 (2007) 653-655
11. S.R.Collins, et al., Functional dissection of protein complexes involved in yeast chromosome biology using a genetic interaction map, Nature. Available online 21 February 2007.
12. Onoda F., Seki M., Miyajima A., and Enomoto T. Elevation of sister chromatid exchange in Saccharomyces cerevisiae sgs1 disruptants and the relevance of the disruptants as a system to evaluate mutations in Bloom's syndrome gene. Mutat. Res. 459 (2000) 203-209
13. Ui A., Seki M., Ogiwara H., Onodera R., Fukushige S., Onoda F., and Enomoto T. The ability of Sgs1 to interact with DNA topoisomerase III is essential for damage-induced recombination. DNA Repair 4 (2005) 191-201
14. Ellis N.A., Groden J., Ye T.Z., Straughen J., Lennon D.J., Ciocci S., Proytcheva M., and German J. The Bloom's syndrome gene product is homologous to RecQ helicases. Cell 83 (1995) 655-666
15. German J. Bloom syndrome: a mendelian prototype of somatic mutational disease. Medicine 72 (1993) 393-406
16. Cobb J.A., Schleker T., Rojas V., Bjergbaek L., Tercero J.A., and Gasser J.M. Replisome instability, fork collapse, and gross chromosomal rearrangements arise synergistically from Mec1 kinase and RecQ helicase mutations. Genes Dev. 19 (2005) 3055-3069
17. Onoda F F., Seki M M., Wang W., and Enomoto T. The hyper unequal sister chromatid recombination in an sgs1 mutant of budding yeast requires MSH2. DNA Repair 3 (2004) 1355-1362
18. Longtine M.S., McKenzie A., Demarini D.J., Shah N.G., Wach A., Brachat A., Philippsen P., and Pringle J.R. Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae. Yeast 14 (1998) 953-961
19. Fabre F., Chan A., Heyer W.D., and Gangloff S. Alternate pathways involving Sgs1/Top3, Mus81/ Mms4, and Srs2 prevent formation of toxic recombination intermediates from single-stranded gaps created by DNA replication. Proc. Natl. Acad. Sci. USA 99 (2002) 16887-16892
20. Luke B., Versini G., Jaquenoud M., Zaidi I.W., and Kurz T. The cullin Rtt101p promotes replication fork progression through damaged DNA and natural pause sites. Curr. Biol. 16 (2006) 786-792
21. Ho Y., et al. Systematic identification of protein complexes in Saccharomyces cerevisiae by mass spectrometry. Nature 415 (2002) 180-183
22. Krogan N.J., et al. Global landscape of protein complexes in the yeast Saccharomyces cerevisiae. Nature 440 (2006) 637-643
23. Prakash L., and Prakash S. Isolation and characterization of MMS-sensitive mutants of Saccharomyces cerevisiae. Genetics 86 (1977) 33-55
24. Liberi G., Maffioletti G., Lucca D., Chiolo I., Baryshnikova A., Cotta-Ramusino C., Lopes M., Pellicioli A., Haber J.E., and Foiani M. Rad51-dependent DNA structures accumulate at damaged replication forks in sgs1 mutants defective in the yeast ortholog of BLM RecQ helicase. Genes Dev. 19 (2005) 339-350
25. Haber J.E. DNA recombination: the replication connection. Trends Biochem. Sci. 24 (1999) 271-275