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The first mouse mutants of D14Abb1e (Fam208a) show that it is critical for early development

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    SYSNO ASEP0435131
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleThe first mouse mutants of D14Abb1e (Fam208a) show that it is critical for early development
    Author(s) Harten, S.K. (AU)
    Bruxner, T.J. (AU)
    Bharti, V. (AU)
    Blewitt, M. (AU)
    Nguyen, T.M.T. (AU)
    Whitelaw, E. (AU)
    Epp, Trevor (UMG-J) RID
    Source TitleMammalian Genome. - : Springer - ISSN 0938-8990
    Roč. 25, 7-8 (2014), s. 293-303
    Number of pages11 s.
    Languageeng - English
    CountryUS - United States
    Keywordsembryogenesis ; forward genetics ; mouse mutant
    Subject RIVEB - Genetics ; Molecular Biology
    Institutional supportUMG-J - RVO:68378050
    UT WOS000339875100002
    DOI10.1007/s00335-014-9516-0
    AnnotationAn ENU mutagenesis screen to identify novel epigenetic modifiers was established in mice carrying a multi-copy GFP transgene, which is expressed in a variegated manner in erythrocytes and is highly sensitive to epigenetic silencing. The screen has produced mouse mutants of both known modifiers of epigenetic state, such as Dnmt1 and Smarca5, and novel modifiers, such as Smchd1 and Rlf. Here we report two mouse lines generated from the screen, MommeD6 and MommeD20, with point mutations in D14Abb1e. These are the first mouse mutants of D14Abb1e (also known as Fam208a), a gene about which little is known. Heterozygous intercrosses show that homozygous mutants from both the MommeD6 and MommeD20 lines are not viable beyond gastrulation, demonstrating an important role for D14Abb1e in development. We demonstrate that haploinsufficiency for D14Abb1e effects transgene expression at the RNA level. Analysis of the predicted D14Abb1e protein sequence reveals that it contains putative nuclear localisation signals and a domain of unknown function, DUF3715. Our studies reveal that D14Abb1e is localised to the nucleus and is expressed in skin and testes.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2015
Number of the records: 1  

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