Brain abnormalities, defective meiotic chromosome synapsis and female subfertility in HSF2 null mice

Marko Kallio, YH Chang, M Manuel, TP Alastalo, M Rallu, Y Gitton, L Pirkkala, MT Loones, L Paslaru, S Larney, S Hiard, M Morange, Lea Sistonen, V Mezger

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    124 Sitaatiot (Scopus)

    Abstrakti

    Heat shock factor 2, one of the four vertebrate HSFs, transcriptional regulators of heat shock gene expression, is active during embryogenesis and spermatogenesis, with unknown functions and targets. By disrupting the Hsf2 gene, we show that, although the lack of HSF2 is not embryonic lethal, Hsf2(-/-) mice suffer from brain abnormalities, and meiotic and gameto genesis defects in both genders. The disturbances in brain are characterized by the enlargement of lateral and third ventricles and the reduction of hippocampus and striatum, in correlation with HSF2 expression in proliferative cells of the neuroepithelium and in some ependymal cells in adults. Many developing spermatocytes are eliminated via apoptosis in a stage-specific manner in Hsf2(-/-) males, and pachytene spermatocytes also display structural defects in the synaptonemal complexes between homologous chromosomes. Hsf2(-/-) females suffer from multiple fertility defects: the production of abnormal eggs, the reduction in ovarian follicle number and the presence of hemorrhagic cystic follicles are consistent with meiotic defects. Hsf2(-/-) females also display hormone response defects, that can be rescued by superovulation treatment, and exhibit abnormal rates of luteinizing hormone receptor mRNAs.
    AlkuperäiskieliEi tiedossa
    Sivut2591–2601
    Sivumäärä11
    JulkaisuEMBO Journal
    Vuosikerta21
    Numero11
    TilaJulkaistu - 2002
    OKM-julkaisutyyppiA1 Julkaistu artikkeli, soviteltu

    Keywords

    • apoptosis
    • brain defects
    • gametogenesis
    • HSF2
    • synaptonemal complex

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