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Resection of DNA double-strand breaks activates Mre11- Rad50- Nbs1- and Rad9- Hus1- Rad1-dependent mechanisms that redundantly promote ATR checkpoint activation and end processing in Xenopus egg extracts. , Tatsukawa K., Nucleic Acids Res. February 13, 2024;
Profiling ubiquitin signalling with UBIMAX reveals DNA damage- and SCFβ-Trcp1-dependent ubiquitylation of the actin-organizing protein Dbn1. , Colding-Christensen CS., Nat Commun. December 14, 2023; 14 (1): 8293.
POLθ prevents MRE11- NBS1- CtIP-dependent fork breakage in the absence of BRCA2/RAD51 by filling lagging-strand gaps. , Mann A., Mol Cell. November 17, 2022; 82 (22): 4218-4231.e8.
MRN-dependent and independent pathways for recruitment of TOPBP1 to DNA double-strand breaks. , Montales K., PLoS One. August 2, 2022; 17 (8): e0271905.
Mre11 exonuclease activity promotes irreversible mitotic progression under replication stress. , Hashimoto Y., Life Sci Alliance. March 15, 2022; 5 (6):
Structure-function analysis of TOPBP1's role in ATR signaling using the DSB-mediated ATR activation in Xenopus egg extracts (DMAX) system. , Montales K., Sci Rep. January 11, 2021; 11 (1): 467.
RPA-coated single-stranded DNA promotes the ETAA1-dependent activation of ATR. , Lyu K., Cell Cycle. April 1, 2019; 18 (8): 898-913.
Fanconi-Anemia-Associated Mutations Destabilize RAD51 Filaments and Impair Replication Fork Protection. , Zadorozhny K., Cell Rep. October 10, 2017; 21 (2): 333-340.
Smarcal1-Mediated Fork Reversal Triggers Mre11-Dependent Degradation of Nascent DNA in the Absence of Brca2 and Stable Rad51 Nucleofilaments. , Kolinjivadi AM., Mol Cell. September 7, 2017; 67 (5): 867-881.e7.
Cip29 is phosphorylated following activation of the DNA damage response in Xenopus egg extracts. , Holden J., PLoS One. July 10, 2017; 12 (7): e0181131.
Mdc1 modulates the interaction between TopBP1 and the MRN complex during DNA damage checkpoint responses. , Choi SH., Biochem Biophys Res Commun. October 7, 2016; 479 (1): 5-11.
Xenopus Mcm10 is a CDK-substrate required for replication fork stability. , Chadha GS., Cell Cycle. August 17, 2016; 15 (16): 2183-2195.
The structure of ends determines the pathway choice and Mre11 nuclease dependency of DNA double-strand break repair. , Liao S., Nucleic Acids Res. July 8, 2016; 44 (12): 5689-701.
Suppression of DNA-damage checkpoint signaling by Rsk-mediated phosphorylation of Mre11. , Chen C ., Proc Natl Acad Sci U S A. December 17, 2013; 110 (51): 20605-10.
The Mre11- Rad50- Nbs1 (MRN) complex has a specific role in the activation of Chk1 in response to stalled replication forks. , Lee J ., Mol Biol Cell. May 1, 2013; 24 (9): 1343-53.
A role for the MRN complex in ATR activation via TOPBP1 recruitment. , Duursma AM., Mol Cell. April 11, 2013; 50 (1): 116-22.
The MRN- CtIP pathway is required for metaphase chromosome alignment. , Rozier L., Mol Cell. March 28, 2013; 49 (6): 1097-107.
Analysis of MRE11's function in the 5'-->3' processing of DNA double-strand breaks. , Liao S., Nucleic Acids Res. May 1, 2012; 40 (10): 4496-506.
Time-dependent predominance of nonhomologous DNA end-joining pathways during embryonic development in mice. , Chiruvella KK., J Mol Biol. March 30, 2012; 417 (3): 197-211.
Role for Rif1 in the checkpoint response to damaged DNA in Xenopus egg extracts. , Kumar S ., Cell Cycle. March 15, 2012; 11 (6): 1183-94.
RAD51- and MRE11-dependent reassembly of uncoupled CMG helicase complex at collapsed replication forks. , Hashimoto Y., Nat Struct Mol Biol. December 4, 2011; 19 (1): 17-24.
Cdk1 uncouples CtIP-dependent resection and Rad51 filament formation during M-phase double-strand break repair. , Peterson SE., J Cell Biol. September 5, 2011; 194 (5): 705-20.
CtIP interacts with TopBP1 and Nbs1 in the response to double-stranded DNA breaks (DSBs) in Xenopus egg extracts. , Ramírez-Lugo JS., Cell Cycle. February 1, 2011; 10 (3): 469-80.
Replication protein A promotes 5'-->3' end processing during homology-dependent DNA double-strand break repair. , Yan H., J Cell Biol. January 24, 2011; 192 (2): 251-61.
Rad51 protects nascent DNA from Mre11-dependent degradation and promotes continuous DNA synthesis. , Hashimoto Y., Nat Struct Mol Biol. November 1, 2010; 17 (11): 1305-11.
Xenopus DNA2 is a helicase/nuclease that is found in complexes with replication proteins And-1/ Ctf4 and Mcm10 and DSB response proteins Nbs1 and ATM. , Wawrousek KE., Cell Cycle. March 15, 2010; 9 (6): 1156-66.
The Mre11/ Rad50/ Nbs1 complex functions in resection-based DNA end joining in Xenopus laevis. , Taylor EM., Nucleic Acids Res. January 1, 2010; 38 (2): 441-54.
CtIP links DNA double-strand break sensing to resection. , You Z., Mol Cell. December 25, 2009; 36 (6): 954-69.
The Mre11- Rad50- Nbs1 complex mediates activation of TopBP1 by ATM. , Yoo HY., Mol Biol Cell. May 1, 2009; 20 (9): 2351-60.
Ku80 removal from DNA through double strand break-induced ubiquitylation. , Postow L., J Cell Biol. August 11, 2008; 182 (3): 467-79.
Mre11- Rad50- Nbs1-dependent processing of DNA breaks generates oligonucleotides that stimulate ATM activity. , Jazayeri A., EMBO J. July 23, 2008; 27 (14): 1953-62.
ATM and ATR promote Mre11 dependent restart of collapsed replication forks and prevent accumulation of DNA breaks. , Trenz K., EMBO J. April 19, 2006; 25 (8): 1764-74.
Repair of double-strand breaks by nonhomologous end joining in the absence of Mre11. , Di Virgilio M., J Cell Biol. December 5, 2005; 171 (5): 765-71.
ATM activation and its recruitment to damaged DNA require binding to the C terminus of Nbs1. , You Z., Mol Cell Biol. July 1, 2005; 25 (13): 5363-79.
Mre11 assembles linear DNA fragments into DNA damage signaling complexes. , Costanzo V., PLoS Biol. May 1, 2004; 2 (5): E110.