Small Rad51 and Dmc1 Complexes Often Co-occupy Both Ends of a Meiotic DNA Double Strand Break-Reference-Cited by-同舟云学术

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Small Rad51 and Dmc1 Complexes Often Co-occupy Both Ends of a Meiotic DNA Double Strand Break

Published:2015-12-31 Issue:12 Volume:11 Page:e1005653
ISSN:1553-7404
Container-title:PLOS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Brown M. Scott,Grubb Jennifer,Zhang Annie,Rust Michael J.,Bishop Douglas K.

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics (clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference69 articles.

1. Molecular genetics of recombination;N Hunter,2007

2. DNA Strand Exchange and RecA Homologs in Meiosis;MS Brown;Cold Spring Harb Perspect Biol,2015

3. Catalysis of ATP-dependent homologous DNA pairing and strand exchange by yeast RAD51 protein;P Sung;Science,1994

4. Human Rad51 protein promotes ATP-dependent homologous pairing and strand transfer reactions in vitro;P Baumann;Cell,1996

5. Recombination activities of HsDmc1 protein, the meiotic human homolog of RecA protein;Z Li;Proc Natl Acad Sci U S A,1997

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1. Sae2 controls Mre11 endo- and exonuclease activities by different mechanisms;Nature Communications;2024-08-22

2. The MRE11-RAD50-NBS1 complex both starts and extends DNA end resection in mouse meiosis;2024-08-17

3. FIGNL1-FIRRM is essential for meiotic recombination and prevents DNA damage-independent RAD51 and DMC1 loading;Nature Communications;2024-08-15

4. FIGL1 attenuates meiotic interhomolog repair and is counteracted by RAD51 paralog XRCC2 and chromosome axis protein ASY1 during meiosis;2024-04-28

5. The Dmc1 recombinase physically interacts with and promotes the meiotic crossover functions of the Mlh1–Mlh3 endonuclease;GENETICS;2024-04-24

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