Ensuring meiotic DNA break formation in the mouse pseudoautosomal region

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Acquaviva , L , Boekhout , M , Karasu , M E , Brick , K , Pratto , F , Li , T , van Overbeek , M , Kauppi , L , Camerini-Otero , R D , Jasin , M & Keeney , S 2020 , ' Ensuring meiotic DNA break formation in the mouse pseudoautosomal region ' , Nature , vol. 582 , no. 7812 , pp. 426–431 . https://doi.org/10.1038/s41586-020-2327-4

Title: Ensuring meiotic DNA break formation in the mouse pseudoautosomal region
Author: Acquaviva, Laurent; Boekhout, Michiel; Karasu, Mehmet E.; Brick, Kevin; Pratto, Florencia; Li, Tao; van Overbeek, Megan; Kauppi, Liisa; Camerini-Otero, R. Daniel; Jasin, Maria; Keeney, Scott
Contributor: University of Helsinki, Genome Stability Group
Date: 2020-06
Language: eng
Number of pages: 25
Belongs to series: Nature
ISSN: 0028-0836
URI: http://hdl.handle.net/10138/325615
Abstract: In mice, the pseudoautosomal region of the sex chromosomes undergoes a dynamic structural rearrangement to promote a high rate of DNA double-strand breaks and to ensure X-Y recombination. Sex chromosomes in males of most eutherian mammals share only a small homologous segment, the pseudoautosomal region (PAR), in which the formation of double-strand breaks (DSBs), pairing and crossing over must occur for correct meiotic segregation(1,2). How cells ensure that recombination occurs in the PAR is unknown. Here we present a dynamic ultrastructure of the PAR and identify controlling cis- and trans-acting factors that make the PAR the hottest segment for DSB formation in the male mouse genome. Before break formation, multiple DSB-promoting factors hyperaccumulate in the PAR, its chromosome axes elongate and the sister chromatids separate. These processes are linked to heterochromatic mo-2 minisatellite arrays, and require MEI4 and ANKRD31 proteins but not the axis components REC8 or HORMAD1. We propose that the repetitive DNA sequence of the PAR confers unique chromatin and higher-order structures that are crucial for recombination. Chromosome synapsis triggers collapse of the elongated PAR structure and, notably, oocytes can be reprogrammed to exhibit spermatocyte-like levels of DSBs in the PAR simply by delaying or preventing synapsis. Thus, the sexually dimorphic behaviour of the PAR is in part a result of kinetic differences between the sexes in a race between the maturation of the PAR structure, formation of DSBs and completion of pairing and synapsis. Our findings establish a mechanistic paradigm for the recombination of sex chromosomes during meiosis.
3111 Biomedicine

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