Differential timing and control of noncrossover and crossover recombination during meiosis - PubMed (original) (raw)
Comparative Study
. 2001 Jul 13;106(1):47-57.
doi: 10.1016/s0092-8674(01)00416-0.
Affiliations
- PMID: 11461701
- DOI: 10.1016/s0092-8674(01)00416-0
Free article
Comparative Study
Differential timing and control of noncrossover and crossover recombination during meiosis
T Allers et al. Cell. 2001.
Free article
Abstract
Unitary models of meiotic recombination postulate that a central intermediate containing Holliday junctions is resolved to generate either noncrossover or crossover recombinants, both of which contain heteroduplex DNA. Contrary to this expectation, we find that during meiosis in Saccharomyces cerevisiae, noncrossover heteroduplex products are formed at the same time as Holliday junction intermediates. Crossovers appear later, when these intermediates are resolved. Furthermore, noncrossover and crossover recombination are regulated differently. ndt80 mutants arrest in meiosis with unresolved Holliday junction intermediates and very few crossovers, while noncrossover heteroduplex products are formed at normal levels and with normal timing. These results suggest that crossovers are formed by resolution of Holliday junction intermediates, while most noncrossover recombinants arise by a different, earlier pathway.
Similar articles
- Mechanistic View and Genetic Control of DNA Recombination during Meiosis.
Marsolier-Kergoat MC, Khan MM, Schott J, Zhu X, Llorente B. Marsolier-Kergoat MC, et al. Mol Cell. 2018 Apr 5;70(1):9-20.e6. doi: 10.1016/j.molcel.2018.02.032. Mol Cell. 2018. PMID: 29625041 - Repeated strand invasion and extensive branch migration are hallmarks of meiotic recombination.
Ahuja JS, Harvey CS, Wheeler DL, Lichten M. Ahuja JS, et al. Mol Cell. 2021 Oct 21;81(20):4258-4270.e4. doi: 10.1016/j.molcel.2021.08.003. Epub 2021 Aug 27. Mol Cell. 2021. PMID: 34453891 Free PMC article. - Meiosis. DNA branching during meiotic recombination.
Byers B, Hollingsworth NM. Byers B, et al. Curr Biol. 1994 May 1;4(5):448-51. doi: 10.1016/s0960-9822(00)00100-7. Curr Biol. 1994. PMID: 7922362 Review. - Recombination: Holliday junction resolution and crossover formation.
Heyer WD. Heyer WD. Curr Biol. 2004 Jan 20;14(2):R56-8. doi: 10.1016/j.cub.2003.12.043. Curr Biol. 2004. PMID: 14738748 Review.
Cited by
- Proximity labeling reveals new functional relationships between meiotic recombination proteins in S. cerevisiae.
Voelkel-Meiman K, Liddle JC, Balsbaugh JL, MacQueen AJ. Voelkel-Meiman K, et al. PLoS Genet. 2024 Oct 15;20(10):e1011432. doi: 10.1371/journal.pgen.1011432. eCollection 2024 Oct. PLoS Genet. 2024. PMID: 39405359 Free PMC article. - Multiple independent losses of crossover interference during yeast evolutionary history.
Dutta A, Dutreux F, Garin M, Caradec C, Friedrich A, Brach G, Thiele P, Gaudin M, Llorente B, Schacherer J. Dutta A, et al. PLoS Genet. 2024 Sep 26;20(9):e1011426. doi: 10.1371/journal.pgen.1011426. eCollection 2024 Sep. PLoS Genet. 2024. PMID: 39325820 Free PMC article. - Synaptonemal complex protects double-Holliday junctions during meiosis.
Tang S, Koo J, Pourhosseinzadeh M, Nguyen E, Liu N, Ma C, Lu H, Lee M, Hunter N. Tang S, et al. bioRxiv [Preprint]. 2024 Sep 15:2024.09.14.613089. doi: 10.1101/2024.09.14.613089. bioRxiv. 2024. PMID: 39314413 Free PMC article. Preprint. - Meiotic double-strand break repair DNA synthesis tracts in Arabidopsis thaliana.
Hernández Sánchez-Rebato M, Schubert V, White CI. Hernández Sánchez-Rebato M, et al. PLoS Genet. 2024 Jul 16;20(7):e1011197. doi: 10.1371/journal.pgen.1011197. eCollection 2024 Jul. PLoS Genet. 2024. PMID: 39012914 Free PMC article. - An acidic loop in the forkhead-associated domain of the yeast meiosis-specific kinase Mek1 interacts with a specific motif in a subset of Mek1 substrates.
Weng Q, Wan L, Straker GC, Deegan TD, Duncker BP, Neiman AM, Luk E, Hollingsworth NM. Weng Q, et al. Genetics. 2024 Sep 4;228(1):iyae106. doi: 10.1093/genetics/iyae106. Genetics. 2024. PMID: 38979911
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases