Precursor of human adenovirus core polypeptide Mu targets the nucleolus and modulates the expression of E2 proteins
1 School of Biochemistry and Molecular Biology, University of Leeds, Leeds LS2 9JT, UK 2 Division of Virology, Department of Pathology and Microbiology, University Walk, Bristol University, Bristol BS8 1TD, UK 3 Department of Medical Biochemistry and Microbiology, Uppsala University, Box 582, S-7512...
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Published in | Journal of general virology Vol. 85; no. 1; pp. 185 - 196 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
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Soc General Microbiol
01.01.2004
Society for General Microbiology |
Subjects | |
Online Access | Get full text |
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Summary: | 1 School of Biochemistry and Molecular Biology, University of Leeds, Leeds LS2 9JT, UK
2 Division of Virology, Department of Pathology and Microbiology, University Walk, Bristol University, Bristol BS8 1TD, UK
3 Department of Medical Biochemistry and Microbiology, Uppsala University, Box 582, S-75123 Uppsala, Sweden
Correspondence David Matthews d.a.matthews{at}bristol.ac.uk
We have examined the subcellular localization properties of human adenovirus 2 (HAdV-2) preMu and mature Mu (pX) proteins as fusions with enhanced green fluorescence protein (EGFP). We determined that preMu is exclusively a nucleolar protein with a single nucleolar accumulation signal within the Mu sequence. In addition, we noted that both preMuEGFP and MuEGFP are excluded from adenovirus DNA-binding protein (DBP)-rich replication centres in adenovirus-infected cells. Surprisingly, we observed that cells in which preMuEGFP (but not MuEGFP) is transiently expressed prior to or shortly after infection with Ad2 did not express late adenovirus genes. Further investigation suggested this might be due to a failure to express pre-terminal protein (preTP) from the E2 region, despite expression of another E2 protein, DBP. Deletion mutagenesis identified a highly conserved region in the C terminus of preMu responsible for these observations. Thus our data suggest that preMu may play a role in modulating accumulation of proteins from the E2 region. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0022-1317 1465-2099 1465-2099 |
DOI: | 10.1099/vir.0.19352-0 |