Recruitment and retention dynamics of RECQL5 at DNA double strand break sites
Tài liệu tham khảo
Bohr, 2008, Rising from the RecQ-age: the role of human RecQ helicases in genome maintenance, Trends Biochem. Sci., 33, 609, 10.1016/j.tibs.2008.09.003
Singh, 2009, Roles of RECQ helicases in recombination based DNA repair, genomic stability and aging, Biogerontology, 10, 235, 10.1007/s10522-008-9205-z
D.K. Singh, A.K. Ghosh, D.L. Croteau, V.A. Bohr, RecQ helicases in DNA double strand break repair and telomere maintenance, Mutat. Res. (2011) (Epub ahead of print).
Hickson, 2003, RecQ helicases: caretakers of the genome, Nat. Rev. Cancer, 3, 169, 10.1038/nrc1012
Ichikawa, 2002, Preparation of the gene targeted knockout mice for human premature aging diseases, Werner syndrome, and Rothmund–Thomson syndrome caused by the mutation of DNA helicases, Nihon Yakurigaku Zasshi, 119, 219, 10.1254/fpj.119.219
Lindor, 2000, Rothmund–Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome, Am. J. Med. Genet., 90, 223, 10.1002/(SICI)1096-8628(20000131)90:3<223::AID-AJMG7>3.0.CO;2-Z
Hu, 2007, RECQL5/Recql5 helicase regulates homologous recombination and suppresses tumor formation via disruption of Rad51 presynaptic filaments, Genes Dev., 21, 3073, 10.1101/gad.1609107
Sekelsky, 1999, Drosophila and human RecQ5 exist in different isoforms generated by alternative splicing, Nucleic Acids Res., 27, 3762, 10.1093/nar/27.18.3762
Shimamoto, 2000, Human RecQ5beta, a large isomer of RecQ5 DNA helicase, localizes in the nucleoplasm and interacts with topoisomerases 3alpha and 3beta, Nucleic Acids Res., 28, 1647, 10.1093/nar/28.7.1647
Garcia, 2004, Human RECQ5beta, a protein with DNA helicase and strand-annealing activities in a single polypeptide, EMBO J., 23, 2882, 10.1038/sj.emboj.7600301
Kanagaraj, 2006, Human RECQ5beta helicase promotes strand exchange on synthetic DNA structures resembling a stalled replication fork, Nucleic Acids Res., 34, 5217, 10.1093/nar/gkl677
Ren, 2008, The zinc-binding motif of human RECQ5beta suppresses the intrinsic strand-annealing activity of its DExH helicase domain and is essential for the helicase activity of the enzyme, Biochem. J., 412, 425, 10.1042/BJ20071150
Hu, 2009, Recql5 plays an important role in DNA replication and cell survival after camptothecin treatment, Mol. Biol. Cell, 20, 114, 10.1091/mbc.E08-06-0565
Aygun, 2008, A RECQ5-RNA polymerase II association identified by targeted proteomic analysis of human chromatin, Proc. Natl. Acad. Sci. USA., 105, 8580, 10.1073/pnas.0804424105
Aygun, 2009, Direct inhibition of RNA polymerase II transcription by RECQL5, J. Biol. Chem., 284, 23197, 10.1074/jbc.M109.015750
Islam, 2010, RecQL5 promotes genome stabilization through two parallel mechanisms–interacting with RNA polymerase II and acting as a helicase, Mol. Cell. Biol., 30, 2460, 10.1128/MCB.01583-09
Kanagaraj, 2010, RECQ5 helicase associates with the C-terminal repeat domain of RNA polymerase II during productive elongation phase of transcription, Nucleic Acids Res., 38, 8131, 10.1093/nar/gkq697
Li, 2011, The SET2-RPB1 interaction domain of human RECQ5 is important for transcription-associated genome stability, Mol. Cell. Biol., 31, 2090, 10.1128/MCB.01137-10
Schwendener, 2010, Physical interaction of RECQ5 helicase with RAD51 facilitates its anti-recombinase activity, J. Biol. Chem., 285, 15739, 10.1074/jbc.M110.110478
Speina, 2010, Human RECQL5beta stimulates flap endonuclease 1, Nucleic Acids Res., 38, 2904, 10.1093/nar/gkp1217
Zheng, 2009, MRE11 complex links RECQ5 helicase to sites of DNA damage, Nucleic Acids Res., 37, 2645, 10.1093/nar/gkp147
Ramamoorthy, 2011, RECQL5 cooperates with Topoisomerase II alpha in DNA decatenation and cell cycle progression, Nucleic Acids Res., 40, 1621, 10.1093/nar/gkr844
Nakayama, 2009, Loss of RecQ5 leads to spontaneous mitotic defects and chromosomal aberrations in Drosophila melanogaster, DNA Repair (Amst.), 8, 232, 10.1016/j.dnarep.2008.10.007
Haince, 2008, PARP1-dependent kinetics of recruitment of MRE11 and NBS1 proteins to multiple DNA damage sites, J. Biol. Chem., 283, 1197, 10.1074/jbc.M706734200
Mailand, 2007, RNF8 ubiquitylates histones at DNA double-strand breaks and promotes assembly of repair proteins, Cell, 131, 887, 10.1016/j.cell.2007.09.040
Yano, 2008, Ku recruits XLF to DNA double-strand breaks, EMBO Rep., 9, 91, 10.1038/sj.embor.7401137
Singh, 2010, The involvement of human RECQL4 in DNA double-strand break repair, Aging Cell, 9, 358, 10.1111/j.1474-9726.2010.00562.x
Karmakar, 2006, BLM is an early responder to DNA double-strand breaks, Biochem. Biophys. Res. Commun., 348, 62, 10.1016/j.bbrc.2006.07.037
Lan, 2005, Accumulation of Werner protein at DNA double-strand breaks in human cells, J. Cell Sci., 118, 4153, 10.1242/jcs.02544
Popuri, 2010, Substrate specific stimulation of NEIL1 by WRN but not the other human RecQ helicases, DNA Repair (Amst.), 9, 636, 10.1016/j.dnarep.2010.02.012
Schultz, 2000, p53 binding protein 1 (53BP1) is an early participant in the cellular response to DNA double-strand breaks, J. Cell Biol., 151, 1381, 10.1083/jcb.151.7.1381
Dinant, 2007, Activation of multiple DNA repair pathways by sub-nuclear damage induction methods, J. Cell Sci., 120, 2731, 10.1242/jcs.004523
Liu, 2009, The Werner syndrome protein functions in repair of Cr(VI)-induced replication-associated DNA damage, Toxicol. Sci., 110, 307, 10.1093/toxsci/kfp104
Yankiwski, 2001, The C-terminal domain of the Bloom syndrome DNA helicase is essential for genomic stability, BMC Cell Biol., 2, 11, 10.1186/1471-2121-2-11
Bekker-Jensen, 2005, Dynamic assembly and sustained retention of 53BP1 at the sites of DNA damage are controlled by Mdc1/NFBD1, J. Cell Biol., 170, 201, 10.1083/jcb.200503043
Wen, 2008, A mutant allele of MRE11 found in mismatch repair-deficient tumor cells suppresses the cellular response to DNA replication fork stress in a dominant negative manner, Mol. Biol. Cell, 19, 1693, 10.1091/mbc.E07-09-0975
Dupre, 2008, A forward chemical genetic screen reveals an inhibitor of the Mre11-Rad50-Nbs1 complex, Nat. Chem. Biol., 4, 119, 10.1038/nchembio.63
Gong, 2004, Alpha-amanitin blocks translocation by human RNA polymerase II, J. Biol. Chem., 279, 27422, 10.1074/jbc.M402163200
Karmakar, 2002, Werner protein is a target of DNA-dependent protein kinase in vivo and in vitro, and its catalytic activities are regulated by phosphorylation, J. Biol. Chem., 277, 18291, 10.1074/jbc.M111523200
Patro, 2011, WRN helicase regulates the ATR-CHK1-induced S-phase checkpoint pathway in response to topoisomerase-I-DNA covalent complexes, J. Cell Sci., 124, 3967, 10.1242/jcs.081372
Saintigny, 2002, Homologous recombination resolution defect in werner syndrome, Mol. Cell. Biol., 22, 6971, 10.1128/MCB.22.20.6971-6978.2002
Wu, 2005, The HRDC domain of BLM is required for the dissolution of double Holliday junctions, EMBO J., 24, 2679, 10.1038/sj.emboj.7600740
Kim, 2005, Independent and sequential recruitment of NHEJ and HR factors to DNA damage sites in mammalian cells, J. Cell Biol., 170, 341, 10.1083/jcb.200411083
Chou, 2010, A chromatin localization screen reveals poly (ADP ribose)-regulated recruitment of the repressive polycomb and NuRD complexes to sites of DNA damage, Proc. Natl. Acad. Sci. USA., 107, 18475, 10.1073/pnas.1012946107
Hu, 2005, Recql5 and Blm RecQ DNA helicases have nonredundant roles in suppressing crossovers, Mol. Cell. Biol., 25, 3431, 10.1128/MCB.25.9.3431-3442.2005