Two separable functions of Ctp1 in the early steps of meiotic DNA double-strand break repair
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/43/15/7349/17434132/gkv644.pdf
Reference48 articles.
1. Mre11–Rad50–Nbs1 conformations and the control of sensing, signaling, and effector responses at DNA double-strand breaks
2. The MRE11 complex: starting from the ends
3. Ctp1 CtIP and Rad32 Mre11 Nuclease Activity Are Required for Rec12 Spo11 Removal, but Rec12 Spo11 Removal Is Dispensable for Other MRN-Dependent Meiotic Functions
4. Meiotic DNA Double-Strand Break Repair Requires Two Nucleases, MRN and Ctp1, To Produce a Single Size Class of Rec12 (Spo11)-Oligonucleotide Complexes
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1. A conserved Ctp1/CtIP C-terminal peptide stimulates Mre11 endonuclease activity;Proceedings of the National Academy of Sciences;2021-03-08
2. Distributing meiotic crossovers for optimal fertility and evolution;DNA Repair;2019-09
3. Identification of a miniature Sae2/Ctp1/CtIP ortholog from Paramecium tetraurelia required for sexual reproduction and DNA double-strand break repair;DNA Repair;2019-05
4. CDK contribution to DSB formation and recombination in fission yeast meiosis;PLOS Genetics;2019-01-14
5. Meiotic Double-Strand Break Proteins Influence Repair Pathway Utilization;Genetics;2018-09-21
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