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
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
EE - Microbiology, virology
OECD FORD branch
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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
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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
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