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Translocation of human ribosomal protein S3 to sites of DNA damage is dependant on ERK-mediated phosphorylation following genotoxic stress.

Translocation of human ribosomal protein S3 to sites of DNA damage is dependant on ERK-mediated phosphorylation following genotoxic stress. Research Abstract Details 

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  • Translocation of human ribosomal protein S3 to sites of DNA damage is dependant on ERK-mediated phosphorylation following genotoxic stress. Abstract Text:

    sridevi yadavilliSridevi Yadavilli,vijay hegdeVijay Hegde,walter a deutschWalter A Deutsch,sridevi yadavilliSridevi Yadavilli,vijay hegdeVijay Hegde,walter a deutschWalter A Deutsch,

    Besides its role in translation and ribosome maturation, human ribosomal protein S3 (hS3) is implicated in DNA damage recognition as reflected by its affinity for abasic sites and 7,8-dihydro-8-oxoguanine (8-oxoG) residues in DNA in vitro. Here, we demonstrate that hS3 is capable of carrying out both roles by its ex vivo translocation from the cytoplasm to the nucleus as a consequence of genotoxic stress. The translocation of hS3 is dependent on ERK1/2-mediated phosphorylation of a threonine residue (T42) of hS3. Two different ectopically expressed site-directed mutants of T42 failed to respond to conditions of genotoxic stress, thus providing a link between DNA damage and ERK1/2 dependent phosphorylation of hS3. Lastly, hS3 was traced in exposed cells to its co-localization with 8-oxoG foci, raising the possibility that hS3 is a member of a cellular DNA damage response pathway that results in its interaction with sites of DNA damage.

    Translocation of human ribosomal protein S3 to sites of DNA damage is dependant on ERK-mediated phosphorylation following genotoxic stress. Publishing Authors By Initials

    s yadavilliS Yadavilli,v hegdeV Hegde,wa deutschWA Deutsch,s yadavilliS Yadavilli,v hegdeV Hegde,wa deutschWA Deutsch,

    For similar abstracts research abstracts see: abstracts research

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    Translocation of human ribosomal protein S3 to sites of DNA damage is dependant on ERK-mediated phosphorylation following genotoxic stress. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: DNA repair

    VOLUME: 6

    Page Numbers: 1453-62

    Journal Abbreviation: DNA Repair (Amst.)

    ISSN: 1568-7864

    DAY: 7

    MONTH: 06

    YEAR: 2007

    Translocation of human ribosomal protein S3 to sites of DNA damage is dependant on ERK-mediated phosphorylation following genotoxic stress. Information

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    LANGUAGE: eng

    NlmUniqueID: 101139138

    Translocation of human ribosomal protein S3 to sites of DNA damage is dependant on ERK-mediated phosphorylation following genotoxic stress. Keywords Mesh Terms:

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    Grant and Affiliation Information for Translocation of human ribosomal protein S3 to sites of DNA damage is dependant on ERK-mediated phosphorylation following genotoxic stress.

    AFFILIATION: Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA 70808, USA.

    Country: Netherlands

    Netherlands Research PublicationNetherlands Research Publication

    AGENCY: United States NCI

    GRANT: CA 109798

    ACRONYM: CA

    MEDLINETA: DNA Repair (Amst)

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