The Fission Yeast FANCM Ortholog Directs Non-Crossover Recombination During Meiosis

Author:

Lorenz Alexander1,Osman Fekret1,Sun Weili1,Nandi Saikat1,Steinacher Roland1,Whitby Matthew C.1

Affiliation:

1. Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK

Abstract

No Crossing Over To ensure the correct division of chromosome during the reduction division of meiosis, homologous chromosomes undergo double-strand breaks that—through crossing over and recombination—link the homologs together (and importantly introduce diversity into the genomes of gametes). But only a minority of these crossovers results in recombination—most are directed into non-crossover pathways. Lorenz et al. (p. 1585 ), working in the yeast Schizosaccharomyces pombe , and Crismani et al. (p. 1588 ), working in the higher plant Arabidopsis thaliana , looked for the factors that limit crossovers and promote non-crossover pathways. The homolog of the human Fanconi anemia complementation group M (FANCM) helicase protein was found to be a major meiotic anti-recombinase, which could drive meiotic recombination intermediates into the non-crossover pathway.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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