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Heterochromatin marks HP1gamma, HP1alpha and H3K9me3, and DNA damage response activation in human testis development and germ cell tumours

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    SYSNO ASEP0347140
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleHeterochromatin marks HP1gamma, HP1alpha and H3K9me3, and DNA damage response activation in human testis development and germ cell tumours
    Author(s) Bartkova, J. (DK)
    Moudrý, Pavel (UMG-J)
    Hodný, Zdeněk (UMG-J) RID
    Lukas, J. (DK)
    Rajpert-De Meyts, E. (DK)
    Bártek, Jiří (UMG-J) RID
    Source TitleInternational Journal of Andrology. - : WILEY-BLACKWELL - ISSN 0105-6263
    Roč. 34, 4 Pt 2 (2011), e103-e113
    Number of pages11 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsheterochromatinization ; DNA damage response ; germinal tumours
    Subject RIVEB - Genetics ; Molecular Biology
    R&D ProjectsGA301/08/0353 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z50520514 - UMG-J (2005-2011)
    UT WOS000293174100013
    DOI10.1111/j.1365-2605.2010.01096.x
    AnnotationHeterochromatinization has been implicated in fundamental biological and pathological processes including differentiation, senescence, ageing and tumorigenesis; however, little is known about its regulation and roles in human cells and tissues in vivo. Here, we show distinct cell-type- and cancer-stage-associated patterns of key heterochromatin marks: histone H3 trimethylated at lysine 9 (H3K9me3) and heterochromatic adaptor proteins HP1α and HP1γ, compared with the γH2AX marker of endogenously activated DNA damage response (DDR) and proliferation markers in normal human foetal and adult testes, pre-invasive carcinoma in situ (CIS) lesions and a series of overt germ cell tumours, including seminomas, embryonal carcinomas and teratomas. Among striking findings were high levels of HP1γ in foetal gonocytes, CIS and seminomas; enhanced multimarker heterochromatinization without DDR activation in CIS; and enhanced HP1α in teratoma structures with epithelial and neuronal differentiation.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2012
Number of the records: 1  

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