<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mansouri M</submitter><funding>NIAID NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>1427-40</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC140772</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>77(2)</volume><pubmed_abstract>The genomes of several poxviruses contain open reading frames with homology to the K3 and K5 genes of Kaposi's sarcoma-associated herpesvirus (KSHV) and the K3 gene of murine gammaherpesvirus 68, which target major histocompatibility complex class I (MHC-I) as well as costimulatory molecules for proteasomal or lysosomal degradation. The homologous gene product of myxomavirus (MV), M153R, was recently shown to reduce the cell surface expression of MHC-I. In addition, normal MHC-I surface expression was observed in cells infected with MV lacking M153R (J. L. Guerin, J. Gelfi, S. Boullier, M. Delverdier, F. A. Bellanger, S. Bertagnoli, I. Drexler, G. Sutter, and F. Messud-Petit, J. Virol. 76:2912-2923, 2002). Here, we show that M153R also downregulates the T-cell coreceptor CD4 and we study t</pubmed_abstract><journal>Journal of virology</journal><pubmed_title>The PHD/LAP-domain protein M153R of myxomavirus is a ubiquitin ligase that induces the rapid internalization and lysosomal destruction of CD4.</pubmed_title><pmcid>PMC140772</pmcid><funding_grant_id>AI 49793</funding_grant_id><funding_grant_id>R01 AI048585</funding_grant_id><funding_grant_id>R01 CA094011-01A1</funding_grant_id><funding_grant_id>R01 AI 48585</funding_grant_id><funding_grant_id>R01 AI049793</funding_grant_id><funding_grant_id>R01 CA094011</funding_grant_id><funding_grant_id>R01 CA94011-01A1</funding_grant_id><pubmed_authors>Mansouri M</pubmed_authors><pubmed_authors>Hovey Nerenberg BT</pubmed_authors><pubmed_authors>Bartee E</pubmed_authors><pubmed_authors>Thomas L</pubmed_authors><pubmed_authors>McFadden G</pubmed_authors><pubmed_authors>Thomas G</pubmed_authors><pubmed_authors>Fruh K</pubmed_authors><pubmed_authors>Barrett J</pubmed_authors><pubmed_authors>Gouveia K</pubmed_authors></additional><is_claimable>false</is_claimable><name>The PHD/LAP-domain protein M153R of myxomavirus is a ubiquitin ligase that induces the rapid internalization and lysosomal destruction of CD4.</name><description>The genomes of several poxviruses contain open reading frames with homology to the K3 and K5 genes of Kaposi's sarcoma-associated herpesvirus (KSHV) and the K3 gene of murine gammaherpesvirus 68, which target major histocompatibility complex class I (MHC-I) as well as costimulatory molecules for proteasomal or lysosomal degradation. The homologous gene product of myxomavirus (MV), M153R, was recently shown to reduce the cell surface expression of MHC-I. In addition, normal MHC-I surface expression was observed in cells infected with MV lacking M153R (J. L. Guerin, J. Gelfi, S. Boullier, M. Delverdier, F. A. Bellanger, S. Bertagnoli, I. Drexler, G. Sutter, and F. Messud-Petit, J. Virol. 76:2912-2923, 2002). Here, we show that M153R also downregulates the T-cell coreceptor CD4 and we study t</description><dates><release>2003-01-01T00:00:00Z</release><publication>2003 Jan</publication><modification>2025-04-21T15:28:46.436Z</modification><creation>2019-03-27T00:17:30Z</creation></dates><accession>S-EPMC140772</accession><cross_references><pubmed>12502858</pubmed><doi>10.1128/jvi.77.2.1427-1440.2003</doi></cross_references></HashMap>