Multilayered mechanisms ensure that short chromosomes recombine in meiosis

• Published in: Nature (London) Vol. 582; no. 7810; pp. 124 - 128
• Main Authors: Murakami, Hajime, Lam, Isabel, Huang, Pei-Ching, Song, Jacquelyn, van Overbeek, Megan, Keeney, Scott
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.06.2020; Nature Publishing Group
• Subjects: 45/15; 45/22; 45/23; 45/29; 45/44; 45/70; 45/77; 631/208/212/2304; 631/337/103; 631/337/1427/2122; 631/337/149; 82/1; 82/29; Binding; Centromere - genetics; Centromeres; Chromosome Segregation; Chromosomes; Chromosomes, Fungal - genetics; Chromosomes, Fungal - metabolism; Dissociation; DNA Breaks, Double-Stranded; DNA Replication Timing; Genetic aspects; Genetic recombination; Genetic research; Genomes; Homologous Recombination; Homology; Humanities and Social Sciences; Karyotypes; Meiosis; Meiosis - genetics; Meiotic Prophase I - genetics; multidisciplinary; Physiological aspects; Prophase; Proteins; Recombinases - metabolism; Recombination; Saccharomyces cerevisiae - cytology; Saccharomyces cerevisiae - genetics; Saccharomyces cerevisiae Proteins - metabolism; Science; Science (multidisciplinary); Telomerase; Telomere - genetics; Telomeres; Time Factors; United States
• ISSN: 0028-0836; 1476-4687; 1476-4687
• DOI: 10.1038/s41586-020-2248-2

In most species, homologous chromosomes must recombine in order to segregate accurately during meiosis 1 . Because small chromosomes would be at risk of missegregation if recombination were randomly distributed, the double-strand breaks (DSBs) that initiate recombination are not located arbitrarily 2 . How the nonrandomness of DSB distributions is controlled is not understood, although several pathways are known to regulate the timing, location and number of DSBs. Meiotic DSBs are generated by Spo11 and accessory DSB proteins, including Rec114 and Mer2, which assemble on chromosomes 3 – 7 and are nearly universal in eukaryotes 8 – 11 . Here we demonstrate how Saccharomyces cerevisiae integrates multiple temporally distinct pathways to regulate the binding of Rec114 and Mer2 to chromosomes, thereby controlling the duration of a DSB-competent state. The engagement of homologous chromosomes with each other regulates the dissociation of Rec114 and Mer2 later in prophase I, whereas the timing of replication and the proximity to centromeres or telomeres influence the accumulation of Rec114 and Mer2 early in prophase I. Another early mechanism enhances the binding of Rec114 and Mer2 specifically on the shortest chromosomes, and is subject to selection pressure to maintain the hyperrecombinogenic properties of these chromosomes. Thus, the karyotype of an organism and its risk of meiotic missegregation influence the shape and evolution of its recombination landscape. Our results provide a cohesive view of a multifaceted and evolutionarily constrained system that allocates DSBs to all pairs of homologous chromosomes. Several mechanisms regulate the distribution of double-strand breaks during meiosis in Saccharomyces cerevisiae , ensuring that the shortest chromosomes are able to successfully recombine.