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Prdm9 deficiency of rat oocytes causes synapsis among non-homologous chromosomes and aneuploidy

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    SYSNO ASEP0558062
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitlePrdm9 deficiency of rat oocytes causes synapsis among non-homologous chromosomes and aneuploidy
    Author(s) Gašić, Srdjan (UMG-J)
    Mihola, Ondřej (UMG-J) RID, ORCID
    Trachtulec, Zdeněk (UMG-J) RID, ORCID
    Number of authors3
    Source TitleMammalian Genome. - : Springer - ISSN 0938-8990
    Roč. 33, č. 4 (2022), s. 590-605
    Number of pages16 s.
    Publication formOnline - E
    Languageeng - English
    CountryUS - United States
    Keywordstrisomic pregnancy ; mice lacking ; mouse ; recombination ; age ; meiosis ; protein ; fetal ; gene ; progression
    Subject RIVEB - Genetics ; Molecular Biology
    OECD categoryBiochemistry and molecular biology
    R&D ProjectsGA16-06548S GA ČR - Czech Science Foundation (CSF)
    GA19-06272S GA ČR - Czech Science Foundation (CSF)
    LQ1604 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    LM2015040 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    LM2015062 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    ED1.1.00/02.0109 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    ED2.1.00/19.0395 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    EF16_013/0001775 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Research InfrastructureCESNET II - 90042 - CESNET - zájmové sdružení právnických osob
    Method of publishingLimited access
    Institutional supportUMG-J - RVO:68378050
    UT WOS000799551200001
    DOI10.1007/s00335-022-09954-z
    AnnotationAneuploidy (abnormal chromosome number) accompanies reduced ovarian function in humans and mice, but the reasons behind this concomitance remain underexplored. Some variants in the human gene encoding histone-3-lysine-4,36-trimethyltransferase PRDM9 are associated with aneuploidy, and other variants with ovarian function reduced by premature ovarian failure (POF), but no link between POF and aneuploidy has been revealed. SHR/OlaIpcv rat females lacking PRDM9 manifest POF-a reduced follicle number, litter size, and reproductive age. Here, we explored this model to test how POF relates to oocyte euploidy. The mutant rat females displayed increased oocyte aneuploidy and embryonic death of their offspring compared to controls. Because rat PRDM9 positions meiotic DNA breaks, we investigated the repair of these breaks. Fertile control rodents carry pachytene oocytes with synapsed homologous chromosomes and repaired breaks, while sterile Prdm9-deficient mice carry pachytene-like oocytes with many persisting breaks and asynapsed chromosomes. However, most PRDM9-lacking rat oocytes displayed a few persisting breaks and non-homologous synapsis (NHS). HORMAD2 protein serves as a barrier to sister-chromatid repair and a signal for the synapsis and DNA repair checkpoints. NHS but not asynapsis was associated with HORMAD2 levels similar to the levels on rat pachytene chromosomes with homologous synapsis. NHS was accompanied by crossing-over decreased below the minimum that is essential for euploidy. We argue that the increased mutant rat aneuploidy is due to NHS, which allows some oocytes to pass meiotic checkpoints without one crossing-over per chromosomal pair, leading to segregation errors, and thereby NHS links POF to aneuploidy.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2023
    Electronic addresshttps://link.springer.com/article/10.1007/s00335-022-09954-z
Number of the records: 1  

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