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Hypomethylation of CNG targets induced with dihydroxypropyladenine is rapidly reversed in the course of mitotic cell division in tobacco

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    SYSNO ASEP0126876
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleHypomethylation of CNG targets induced with dihydroxypropyladenine is rapidly reversed in the course of mitotic cell division in tobacco
    Author(s) Koukalová, Blažena (BFU-R)
    Votruba, Ivan (UOCHB-X) RID
    Fojtová, Miloslava (BFU-R) RID, ORCID
    Holý, Antonín (UOCHB-X)
    Kovařík, Aleš (BFU-R) RID, ORCID
    Source TitleTheoretical and Applied Genetics. - : Springer - ISSN 0040-5752
    Roč. 105, č. 5 (2002), s. 796-801
    Number of pages6 s.
    Languageeng - English
    CountryDE - Germany
    Keywordsplant DNA methylation ; S-adenosylhomocysteine hydrolase inhibition ; CNG and CG methylation motifs
    Subject RIVBO - Biophysics
    R&D ProjectsGA521/01/0037 GA ČR - Czech Science Foundation (CSF)
    GP521/01/P042 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z5004920 - BFU-R
    AnnotationWe followed the mitotic transmission of an experimentally induced hypomethylated state of several tobacco repetitive sequences in callus culture and plants. The initial hypomethylation was induced by a hypomethylation drug, dihydroxypropyladenine (DHPA), the competitive inhibitor of cellular S-adenosylhomocysteine hydrolase, which is known to preferentially inhibit methylation at CNG and non-symmetrical motifs while having a negligible effect on methylation at CG motifs. The deprivation of this drug resulted in an almost immediate remethylation of cytosines at CNG motifs (MspI and EcoRII sites) leading us to conclude that, the hypomethylation effect of dihydroxypropyladenine is rather transient and differs from that of 5-azacytidine which often induces heritable changes in methylation patterns. The results suggest that de novo methylation of CNG motifs is a rapid and meiotically independent process on DNA sequences with pre-existing CG methylation.
    WorkplaceInstitute of Biophysics
    ContactJana Poláková, polakova@ibp.cz, Tel.: 541 517 244
    Year of Publishing2003

Number of the records: 1  

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