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Exo1 protects DNA nicks from ligation to promote crossover formation during meiosis.
Gioia, Michael; Payero, Lisette; Salim, Sagar; Fajish V, Ghanim; Farnaz, Amamah F; Pannafino, Gianno; Chen, Jun Jie; Ajith, V P; Momoh, Sherikat; Scotland, Michelle; Raghavan, Vandana; Manhart, Carol M; Shinohara, Akira; Nishant, K T; Alani, Eric.
Afiliación
  • Gioia M; Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
  • Payero L; Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
  • Salim S; School of Biology, Indian Institute of Science Education and Research Thiruvananthapuram, Trivandrum, India.
  • Fajish V G; Institute for Protein Research, Osaka University, Suita, Osaka, Japan.
  • Farnaz AF; School of Biology, Indian Institute of Science Education and Research Thiruvananthapuram, Trivandrum, India.
  • Pannafino G; Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
  • Chen JJ; Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
  • Ajith VP; School of Biology, Indian Institute of Science Education and Research Thiruvananthapuram, Trivandrum, India.
  • Momoh S; Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
  • Scotland M; Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
  • Raghavan V; Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
  • Manhart CM; Department of Chemistry, Temple University, Philadelphia, Pennsylvania, United States of America.
  • Shinohara A; Institute for Protein Research, Osaka University, Suita, Osaka, Japan.
  • Nishant KT; School of Biology, Indian Institute of Science Education and Research Thiruvananthapuram, Trivandrum, India.
  • Alani E; Center for High-Performance Computing, Indian Institute of Science Education and Research Thiruvananthapuram, Trivandrum, India.
PLoS Biol ; 21(4): e3002085, 2023 04.
Article en En | MEDLINE | ID: mdl-37079643
ABSTRACT
In most sexually reproducing organisms crossing over between chromosome homologs during meiosis is essential to produce haploid gametes. Most crossovers that form in meiosis in budding yeast result from the biased resolution of double Holliday junction (dHJ) intermediates. This dHJ resolution step involves the actions of Rad2/XPG family nuclease Exo1 and the Mlh1-Mlh3 mismatch repair endonuclease. Here, we provide genetic evidence in baker's yeast that Exo1 promotes meiotic crossing over by protecting DNA nicks from ligation. We found that structural elements in Exo1 that interact with DNA, such as those required for the bending of DNA during nick/flap recognition, are critical for its role in crossing over. Consistent with these observations, meiotic expression of the Rad2/XPG family member Rad27 partially rescued the crossover defect in exo1 null mutants, and meiotic overexpression of Cdc9 ligase reduced the crossover levels of exo1 DNA-binding mutants to levels that approached the exo1 null. In addition, our work identified a role for Exo1 in crossover interference. Together, these studies provide experimental evidence for Exo1-protected nicks being critical for the formation of meiotic crossovers and their distribution.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas de Saccharomyces cerevisiae Idioma: En Revista: PLoS Biol Asunto de la revista: BIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas de Saccharomyces cerevisiae Idioma: En Revista: PLoS Biol Asunto de la revista: BIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos