Biology Reference
In-Depth Information
60. Mimitou EP, Symington LS. Nucleases and helicases take center stage in homologous
recombination.
Trends Biochem Sci
2009;
34
:264-72.
61. Lisby M, Rothstein R. Choreography of recombination proteins during the DNA damage
response.
DNA Repair (Amst)
2009;
8
:1068-76.
62. Wu D, Topper LM, Wilson TE. Recruitment and dissociation of nonhomologous end joining
proteins
cerevisiae.
Genetics
at
a DNA double-strand break
in Saccharomyces
2008;
178
:1237-49.
63. Dupaigne P, Le Breton C, Fabre F, Gangloff S, Le CamE, Veaute X. The Srs2 helicase activity
is stimulated by Rad51 filaments on dsDNA: implications for crossover incidence during
mitotic recombination.
Mol Cell
2008;
29
:243-54.
64. Lisby M, Barlow JH, Burgess RC, Rothstein R. Choreography of the DNA damage response:
spatiotemporal relationships among checkpoint and repair proteins.
Cell
2004;
118
:699-713.
65. Martin SG, Laroche T, Suka N, Grunstein M, Gasser SM. Relocalization of telomeric Ku and
SIR proteins in response to DNA strand breaks in yeast.
Cell
1999;
97
:621-33.
66. Lengsfeld BM, Rattray AJ, Bhaskara V, Ghirlando R, Paull TT. Sae2 is an endonuclease that
processes hairpin DNA cooperatively with the Mre11/Rad50/Xrs2 complex.
Mol Cell
2007;
28
:638-51.
67. Clerici M, Mantiero D, Lucchini G, Longhese MP. The Saccharomyces cerevisiae Sae2
protein promotes resection and bridging of double strand break ends.
J Biol Chem
2005;
280
:38631-8.
68. Krejci L, Van Komen S, Li Y, et al. DNA helicase Srs2 disrupts the Rad51 presynaptic
filament.
Nature
2003;
423
:305-9.
69. Huertas P, Jackson SP. Human CtIP mediates cell cycle control of DNA end resection and
double strand break repair.
J Biol Chem
2009;
284
:9558-65.
70. Huertas P, Cortes-Ledesma F, Sartori AA, Aguilera A, Jackson SP. CDK targets Sae2 to
control DNA-end resection and homologous recombination.
Nature
2008;
455
:689-92.
71. Huen MS, Chen J. Assembly of checkpoint and repair machineries at DNA damage sites.
Trends Biochem Sci
2010;
35
:101-8.
72. Huen MS, Sy SM, Chen J. BRCA1 and its toolbox for the maintenance of genome integrity.
Nat Rev Mol Cell Biol
2010;
11
:138-48.
73. Khavari PA, Peterson CL, Tamkun JW, Mendel DB, Crabtree GR. BRG1 contains a con-
served domain of the SWI2/SNF2 family necessary for normal mitotic growth and transcrip-
tion.
Nature
1993;
366
:170-4.
74. Shim EY, Chung W-H, Nicolette ML, et al. Saccharomyces cerevisiae Mre11/Rad50/Xrs2 and
Ku proteins regulate association of Exo1 and Dna2 with DNA breaks.
EMBO J
2010;
29
:3370-80.
75. Zhu Z, Chung W-H, Shim EY, Lee SE, Ira G. Sgs1 Helicase and Two Nucleases Dna2 and
Exo1 Resect DNA Double-Strand Break Ends.
Cell
2008;
134
:981-94.
76. Mimitou EP, Symington LS. Sae2, Exo1 and Sgs1 collaborate in DNA double-strand break
processing.
Nature
2008;
455
:770-4.
77. Schaetzlein S, Kodandaramireddy NR, Ju Z, et al. Exonuclease-1 deletion impairs DNA
damage signaling and prolongs
lifespan of
telomere-dysfunctional mice.
Cell
2007;
130
:863-77.
78. Cejka P, Cannavo E, Polaczek P, et al. DNA end resection by Dna2-Sgs1-RPA and its
stimulation by Top3-Rmi1 and Mre11-Rad50-Xrs2.
Nature
2010;
467
:112-6.
79. Niu H, Chung W-H, Zhu Z, et al. Mechanism of the ATP-dependent DNA end-resection
machinery from Saccharomyces cerevisiae.
Nature
2010;
467
:108-11.
80. Nimonkar AV, Genschel J, Kinoshita E, et al. BLM-DNA2-RPA-MRN and EXO1-BLM-
RPA-MRN constitute two DNA end resection machineries for human DNA break repair.
Genes Dev
2011;
25
:350-62.
