Plasticity of the Mre11–Rad50–Xrs2–Sae2 nuclease ensemble in the processing of DNA-bound obstacles
Published 2017 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Plasticity of the Mre11–Rad50–Xrs2–Sae2 nuclease ensemble in the processing of DNA-bound obstacles
Authors
Keywords
-
Journal
GENES & DEVELOPMENT
Volume 31, Issue 23-24, Pages 2331-2336
Publisher
Cold Spring Harbor Laboratory
Online
2018-01-11
DOI
10.1101/gad.307900.117
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Non-homologous DNA end joining and alternative pathways to double-strand break repair
- (2017) Howard H. Y. Chang et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- A global view of meiotic double-strand break end resection
- (2017) Eleni P. Mimitou et al. SCIENCE
- MRN, CtIP, and BRCA1 mediate repair of topoisomerase II–DNA adducts
- (2016) Tomas Aparicio et al. JOURNAL OF CELL BIOLOGY
- Mre11 Is Essential for the Removal of Lethal Topoisomerase 2 Covalent Cleavage Complexes
- (2016) Nguyen Ngoc Hoa et al. MOLECULAR CELL
- Interplay between Ku and Replication Protein A in the Restriction of Exo1-mediated DNA Break End Resection
- (2015) Danielle S. Krasner et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Mechanisms and Consequences of Double-Strand DNA Break Formation in Chromatin
- (2015) Wendy J. Cannan et al. JOURNAL OF CELLULAR PHYSIOLOGY
- Mre11-Sae2 and RPA Collaborate to Prevent Palindromic Gene Amplification
- (2015) Sarah K. Deng et al. MOLECULAR CELL
- 53BP1, BRCA1, and the Choice between Recombination and End Joining at DNA Double-Strand Breaks
- (2014) J. M. Daley et al. MOLECULAR AND CELLULAR BIOLOGY
- Sae2 promotes dsDNA endonuclease activity within Mre11–Rad50–Xrs2 to resect DNA breaks
- (2014) Elda Cannavo et al. NATURE
- DNA Damage Sensing by the ATM and ATR Kinases
- (2013) A. Marechal et al. Cold Spring Harbor Perspectives in Biology
- Mating-Type Genes and MAT Switching in Saccharomyces cerevisiae
- (2012) J. E. Haber GENETICS
- CtIP Is Required to Initiate Replication-Dependent Interstrand Crosslink Repair
- (2012) Michelle L. Duquette et al. PLoS Genetics
- Double-Strand Break End Resection and Repair Pathway Choice
- (2011) Lorraine S. Symington et al. Annual Review of Genetics
- Bidirectional resection of DNA double-strand breaks by Mre11 and Exo1
- (2011) Valerie Garcia et al. NATURE
- DNA double-strand breaks and ATM activation by transcription-blocking DNA lesions
- (2010) Olivier Sordet et al. CELL CYCLE
- DNA Topoisomerases and Their Poisoning by Anticancer and Antibacterial Drugs
- (2010) Yves Pommier et al. CHEMISTRY & BIOLOGY
- Hydroxyurea-Stalled Replication Forks Become Progressively Inactivated and Require Two Different RAD51-Mediated Pathways for Restart and Repair
- (2010) Eva Petermann et al. MOLECULAR CELL
- Distinct Requirements for the Rad32Mre11 Nuclease and Ctp1CtIP in the Removal of Covalently Bound Topoisomerase I and II from DNA
- (2009) Edgar Hartsuiker et al. MOLECULAR CELL
- Sgs1 Helicase and Two Nucleases Dna2 and Exo1 Resect DNA Double-Strand Break Ends
- (2008) Zhu Zhu et al. CELL
- The endless tale of non-homologous end-joining
- (2008) Eric Weterings et al. CELL RESEARCH
- Recruitment of Saccharomyces cerevisiae Dnl4-Lif1 Complex to a Double-Strand Break Requires Interactions With Yku80 and the Xrs2 FHA Domain
- (2008) P. L. Palmbos et al. GENETICS
- Recruitment and Dissociation of Nonhomologous End Joining Proteins at a DNA Double-Strand Break in Saccharomyces cerevisiae
- (2008) D. Wu et al. GENETICS
- ATP-dependent Chromatin Remodeling by theSaccharomyces cerevisiaeHomologous Recombination Factor Rdh54
- (2008) YoungHo Kwon et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Sae2, Exo1 and Sgs1 collaborate in DNA double-strand break processing
- (2008) Eleni P. Mimitou et al. NATURE
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started