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211. Buisson R, Dion-Cote A-M, Coulombe Y, et al. Cooperation of breast cancer proteins PALB2
and piccolo BRCA2 in stimulating homologous recombination. Nat Struct Mol Biol
2010; 17 :1247-54.
212. Marston NJ, Richards WJ, Hughes D, Bertwistle D, Marshall CJ, Ashworth A. Interaction
between the product of the breast cancer susceptibility gene BRCA2 and DSS1, a protein
functionally conserved from yeast to mammals. Mol Cell Biol 1999; 19 :4633-42.
213. Gudmundsdottir K, Lord CJ, Witt E, Tutt ANJ, Ashworth A. DSS1 is required for RAD51
focus formation and genomic stability in mammalian cells. EMBO Rep 2004; 5 :989-93.
214. Kojic M, Yang H, Kostrub CF, Pavletich NP, Holloman WK. The BRCA2-interacting protein
DSS1 is vital for DNA repair, recombination, and genome stability in Ustilago maydis. Mol
Cell 2003; 12 :1043-9.
215. Yang H, Jeffrey PD, Miller J, et al. BRCA2 function in DNA binding and recombination from
a BRCA2-DSS1-ssDNA structure. Science 2002; 297 :1837-48.
216. Zhou Q, Kojic M, Cao Z, Lisby M, Mazloum NA, Holloman WK. Dss1 interaction with Brh2
as a regulatory mechanism for recombinational repair. Mol Cell Biol 2007; 27 :2512-26.
217. Mazloum N, Holloman WK. Second-end capture in DNA double-strand break repair
promoted by Brh2 protein of Ustilago maydis. Mol Cell 2009; 33 :160-70.
218. Thorslund T, McIlwraith MJ, Compton SA, et al. The breast cancer tumor suppressor BRCA2
promotes the specific targeting of RAD51 to single-stranded DNA. Nat Struct Mol Biol
2010; 17 :1263-5.
219. Liu J, Doty T, Gibson B, Heyer W-D. Human BRCA2 protein promotes RAD51 filament
formation on RPA-covered single-stranded DNA. Nat Struct Mol Biol 2010; 17 :1260-2.
220. Lin Z, Kong H, Nei M, Ma H. Origins and evolution of the recA/RAD51 gene family:
evidence for ancient gene duplication and endosymbiotic gene transfer. Proc Natl Acad Sci
USA 2006; 103 :10328-33.
221. Lovett ST. Sequence of the RAD55 gene of Saccharomyces cerevisiae: similarity of RAD55 to
prokaryotic RecA and other RecA-like proteins. Gene 1994; 142 :103-6.
222. Kans JA, Mortimer RK. Nucleotide sequence of the RAD57 gene of Saccharomyces cerevi-
siae. Gene 1991; 105 :139-40.
223. Hays SL, Firmenich AA, Berg P. Complex formation in yeast double-strand break
repair: participation of Rad51, Rad52, Rad55, and Rad57 proteins. Proc Natl Acad Sci
1995; 92 :6925-9.
224. Johnson R, Symington L. Functional differences and interactions among the putative RecA
homologs Rad51, Rad55, and Rad57. Mol Cell Biol 1995; 15 :4843-50.
225. Janke R, Herzberg K, Rolfsmeier M, et al. A truncated DNA-damage-signaling response is
activated after DSB formation in the G1 phase of Saccharomyces cerevisiae. Nucleic Acids Res
2010; 38 :2302-13.
226. Herzberg K, Bashkirov VI, Rolfsmeier M, et al. Phosphorylation of Rad55 on serines 2, 8, and
14 is required for efficient homologous recombination in the recovery of stalled replication
forks. Mol Cell Biol 2006; 26 :8396-409.
227. Bashkirov VI, King JS, Bashkirova EV, Schmuckli-Maurer J, Heyer W-D. DNA repair protein
Rad55 is a terminal
substrate of
the DNA damage checkpoints. Mol Cell Biol
2000; 20 :4393-404.
228. Tsutsui Y, Morishita T, Iwasaki H, Toh H, Shinagawa H. A recombination repair gene of
Schizosaccharomyces pombe, rhp57, is a functional homolog of the Saccharomyces cerevisiae
RAD57 gene and is phylogenetically related to the human XRCC3 gene. Genetics
2000; 154 :1451-61.
229. Khasanov FK, Savchenko GV, Bashkirova EV, Korolev VG, Heyer W-D, Bashkirov VI. A new
recombinational DNA repair gene from Schizosaccharomyces pombe with homology to
Escherichia coli RecA. Genetics 1999; 152 :1557-72.
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