Other names published for SRS2: RADH, RADH1, HPR5, YJL092W
SRS2 LITERATURE TOPICS
- Curated Literature
- Additional Literature
- All Curated References
- Primary Literature
- Reviews
- Genetics/Cell Biology
- Nucleic Acid Information
- Gene Product Information
- Related Genes/Proteins
- Research Aids
- Genome-wide Analysis
- Proteome-wide Analysis
- Other Topics
- Additional Information
SRS2 - Primary Literature (107)
| Reference | Other Genes Addressed |
|---|---|
| Burkovics P, et al. (2013) Srs2 mediates PCNA-SUMO-dependent inhibition of DNA repair synthesis. EMBO J 32(5):742-55 | |
| Dornfeld K (2013) Antifolate Response in Replication Arrest Mutants of Saccharomyces cerevisiae. Anticancer Res 33(5):2037-41 | |
| Huang D, et al. (2013) The Preference for Error-Free or Error-Prone Postreplication Repair in Saccharomyces cerevisiae Exposed to Low-Dose Methyl Methanesulfonate Is Cell Cycle Dependent. Mol Cell Biol 33(8):1515-27 | |
| Mitchel K, et al. (2013) Heteroduplex DNA position defines the roles of the sgs1, srs2, and mph1 helicases in promoting distinct recombination outcomes. PLoS Genet 9(3):e1003340 | |
| Anand RP, et al. (2012) Overcoming natural replication barriers: differential helicase requirements. Nucleic Acids Res 40(3):1091-105 | |
| Armstrong AA, et al. (2012) Recognition of SUMO-modified PCNA requires tandem receptor motifs in Srs2. Nature 483(7387):59-63 | |
| Eckert-Boulet N, et al. (2012) Optimization of ordered plasmid assembly by gap repair in Saccharomyces cerevisiae. Yeast 29(8):323-34 | |
| Kolesar P, et al. (2012) Dual roles of the SUMO-interacting motif in the regulation of Srs2 sumoylation. Nucleic Acids Res 40(16):7831-43 | |
| Marini V and Krejci L (2012) Unwinding of synthetic replication and recombination substrates by Srs2. DNA Repair (Amst) 11(10):789-98 | |
| Miura T, et al. (2012) Homologous recombination via synthesis-dependent strand annealing in yeast requires the Irc20 and Srs2 DNA helicases. Genetics 191(1):65-78 | |
| Mukherjee K and Storici F (2012) A mechanism of gene amplification driven by small DNA fragments. PLoS Genet 8(12):e1003119 | |
| Stead BE, et al. (2012) Mcm2 phosphorylation and the response to replicative stress. BMC Genet 13(1):36 | |
| Tripathi K, et al. (2012) Nicotinamide induces Fob1-dependent plasmid integration into chromosome XII in Saccharomyces cerevisiae. FEMS Yeast Res 12(8):949-57 | |
| Bernstein KA, et al. (2011) The Shu complex, which contains Rad51 paralogues, promotes DNA repair through inhibition of the Srs2 anti-recombinase. Mol Biol Cell 22(9):1599-607 | |
| Leon Ortiz AM, et al. (2011) Srs2 overexpression reveals a helicase-independent role at replication forks that requires diverse cell functions. DNA Repair (Amst) 10(5):506-17 | |
| Liu J, et al. (2011) Rad51 paralogues Rad55-Rad57 balance the antirecombinase Srs2 in Rad51 filament formation.LID - 10.1038/nature10522 [doi] Nature () | |
| Yeung M and Durocher D (2011) Srs2 enables checkpoint recovery by promoting disassembly of DNA damage foci from chromatin. DNA Repair (Amst) 10(12):1213-22 | |
| Dotiwala F, et al. (2010) Mad2 Prolongs DNA Damage Checkpoint Arrest Caused by a Double-Strand Break via a Centromere-Dependent Mechanism. Curr Biol 20(4):328-332 | |
| Hishida T, et al. (2010) Srs2 plays a critical role in reversible G2 arrest upon chronic and low doses of UV irradiation via two distinct homologous recombination-dependent mechanisms in postreplication repair-deficient cells. Mol Cell Biol 30(20):4840-50 | |
| Manthey GM and Bailis AM (2010) Rad51 Inhibits Translocation Formation by Non-Conservative Homologous Recombination in Saccharomyces cerevisiae. PLoS One 5(7):e11889 | |
| Moriel-Carretero M and Aguilera A (2010) A Postincision-Deficient TFIIH Causes Replication Fork Breakage and Uncovers Alternative Rad51- or Pol32-Mediated Restart Mechanisms. Mol Cell 37(5):690-701 | |
| Parnas O, et al. (2010) Elg1, an alternative subunit of the RFC clamp loader, preferentially interacts with SUMOylated PCNA. EMBO J 29(15):2611-22 | |
| Saponaro M, et al. (2010) Cdk1 targets srs2 to complete synthesis-dependent strand annealing and to promote recombinational repair. PLoS Genet 6(2):e1000858 | |
| Schmidt KH, et al. (2010) Defects in DNA lesion bypass lead to spontaneous chromosomal rearrangements and increased cell death. Eukaryot Cell 9(2):315-24 | |
| Antony E, et al. (2009) Srs2 disassembles Rad51 filaments by a protein-protein interaction triggering ATP turnover and dissociation of Rad51 from DNA. Mol Cell 35(1):105-15 | |
| Burgess RC, et al. (2009) Localization of recombination proteins and Srs2 reveals anti-recombinase function in vivo. J Cell Biol 185(6):969-81 | |
| Carter SD, et al. (2009) Nej1 recruits the Srs2 helicase to DNA double-strand breaks and supports repair by a single-strand annealing-like mechanism. Proc Natl Acad Sci U S A 106(29):12037-42 | |
| Colavito S, et al. (2009) Functional significance of the Rad51-Srs2 complex in Rad51 presynaptic filament disruption. Nucleic Acids Res 37(20):6754-64 | |
| Fung CW, et al. (2009) Suppression of the Double-Strand-Break-Repair Defect of the Saccharomyces cerevisiae rad57 Mutant. Genetics 181(4):1195-206 | |
| Kats ES, et al. (2009) The Saccharomyces cerevisiae Rad6 postreplication repair and Siz1/Srs2 homologous recombination-inhibiting pathways process DNA damage that arises in asf1 mutants. Mol Cell Biol 29(19):5226-37 |



