Number of the records: 1  

Chromosomal rearrangement interferes with meiotic X chromosome inactivation

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    SYSNO ASEP0090940
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleChromosomal rearrangement interferes with meiotic X chromosome inactivation
    TitleChromozomální přestavba interferuje s meiotickou inaktivací chromozomu X
    Author(s) Homolka, David (UMG-J)
    Ivánek, Robert (UMG-J)
    Čapková, Jana (UMG-J)
    Jansa, Petr (UMG-J) RID
    Forejt, Jiří (UMG-J) RID, ORCID
    Source TitleGenome Research. - : Cold Spring Harbor Laboratory Press - ISSN 1088-9051
    Roč. 17, č. 10 (2007), s. 1431-1437
    Number of pages7 s.
    Languageeng - English
    CountryUS - United States
    Keywordschromosomal translocations ; meiotic X chromosome inactivation ; spermatogenesis
    Subject RIVEB - Genetics ; Molecular Biology
    R&D Projects1M0520 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    GA301/06/1334 GA ČR - Czech Science Foundation (CSF)
    GA301/07/1383 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z50520514 - UMG-J (2005-2011)
    AnnotationHeterozygosity for certain mouse and human chromosomal rearrangements is characterized by the incomplete meiotic synapsis of rearranged chromosomes, by their colocalization with the XY body in primary spermatocytes, and by male-limited sterility. Here, we report on the transcriptional down-regulation of genes within the unsynapsed region of the rearranged mouse chromosome 17, and on the subsequent disturbance of X chromosome inactivation. The partial transcriptional suppression of genes in the unsynapsed chromatin was most prominent prior to the mid-pachytene stage of primary spermatocytes. Later, during the mid-late pachytene, the rearranged autosomes colocalized with the XY body, and the X chromosome failed to undergo proper transcriptional silencing. Our findings provide direct evidence on the MSUC acting at the mRNA level, and implicate that autosomal asynapsis in meiosis may cause male sterility by interfering with meiotic sex chromosome inactivation.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2008
Number of the records: 1  

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