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Polyomavirus Middle T-Antigen Is a Transmembrane Protein That Binds Signaling Proteins in Discrete Subcellular Membrane Sites

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F11%3A10106664" target="_blank" >RIV/00216208:11310/11:10106664 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1128/JVI.02209-10" target="_blank" >http://dx.doi.org/10.1128/JVI.02209-10</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1128/JVI.02209-10" target="_blank" >10.1128/JVI.02209-10</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Polyomavirus Middle T-Antigen Is a Transmembrane Protein That Binds Signaling Proteins in Discrete Subcellular Membrane Sites

  • Original language description

    Murine polyomavirus middle T-antigen (MT) induces tumors by mimicking an activated growth factor receptor. An essential component of this action is a 22-amino-acid hydrophobic region close to the C terminus which locates MT to cell membranes. Here, we demonstrate that this sequence is a transmembrane domain (TMD) by showing that a hemagglutinin (HA) tag added to the MT C terminus is exposed on the outside of the cells, with the N terminus inside. The mutant protein with addition of the ER retention signal KDEL to the MT C terminus, locates only in the ER, demonstrating that MT does insert into membranes solely at this location. In addition, this ER-located MT failed to transform. MTKDEL protein failed to interact with ShcA, phosphatidylinositol 3-kinase (PI3K), and phospholipase C-1 (PLC-1), despite being tyrosine phosphorylated. Additional studies showed that MT binding to PP2A is probably required for MT to ef?ciently exit the ER and migrate to the plasma membrane. Overall, these dat

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EE - Microbiology, virology

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2011

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Virology

  • ISSN

    0022-538X

  • e-ISSN

  • Volume of the periodical

    85

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    9

  • Pages from-to

    3046-3054

  • UT code for WoS article

    000288373000001

  • EID of the result in the Scopus database