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The actin family member Arp6 and the histone variant H2A.Z are required for spatial positioning of chromatin in chicken cell nuclei

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    SYSNO ASEP0387825
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleThe actin family member Arp6 and the histone variant H2A.Z are required for spatial positioning of chromatin in chicken cell nuclei
    Author(s) Maruyama, E.O. (JP)
    Hori, T. (JP)
    Tanabe, H. (JP)
    Kitamura, H. (JP)
    Matsuda, R. (JP)
    Tone, S. (JP)
    Hozák, Pavel (UMG-J) RID, ORCID
    Habermann, F.A. (DE)
    von Hase, J. (DE)
    Cremer, C. (DE)
    Fukagawa, T. (JP)
    Harata, M. (JP)
    Source TitleJournal of Cell Science. - : Company of Biologists - ISSN 0021-9533
    Roč. 125, č. 16 (2012), s. 3739-3744
    Number of pages6 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsactin-related protein ; histone variant ; nuclear organization
    Subject RIVEB - Genetics ; Molecular Biology
    R&D ProjectsLC545 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    LH12143 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Institutional supportUMG-J - RVO:68378050
    UT WOS000309525300006
    DOI10.1242/jcs.103903
    AnnotationThe spatial organization of chromatin in the nucleus contributes to genome function and is altered during the differentiation of normal and tumorigenic cells. Although nuclear actin-related proteins (Arps) have roles in the local alteration of chromatin structure, it is unclear whether they are involved in the spatial positioning of chromatin. In the interphase nucleus of vertebrate cells, gene-dense and gene-poor chromosome territories (CTs) are located in the center and periphery, respectively. We analyzed chicken DT40 cells in which Arp6 had been knocked out conditionally, and showed that the radial distribution of CTs was impaired in these knockout cells. Arp6 is an essential component of the SRCAP chromatin remodeling complex, which deposits the histone variant H2A.Z into chromatin. The redistribution of CTs was also observed in H2A. Z-deficient cells for gene-rich microchromosomes, but to lesser extent for gene-poor macrochromosomes. These results indicate that Arp6 and H2A.Z contribute to the radial distribution of CTs through different mechanisms. Microarray analysis suggested that the localization of chromatin to the nuclear periphery per se is insufficient for the repression of most genes.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2013
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