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Precursor of human adenovirus core polypeptide Mu targets the nucleolus and modulates the expression of E2 proteins

Lee, T W R (author)
Lawrence, F J (author)
Dauksaite, V (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
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Akusjärvi, Göran (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Blair, G E (author)
Matthews, D A (author)
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 (creator_code:org_t)
Microbiology Society, 2004
2004
English.
In: Journal of General Virology. - : Microbiology Society. - 0022-1317 .- 1465-2099. ; 85:Pt 1, s. 185-196
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • 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 preMu-EGFP and Mu-EGFP are excluded from adenovirus DNA-binding protein (DBP)-rich replication centres in adenovirus-infected cells. Surprisingly, we observed that cells in which preMu-EGFP (but not Mu-EGFP) 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.

Keyword

Adenovirus E2 Proteins/*metabolism
Adenoviruses; Human/pathogenicity
Amino Acid Sequence
Cell Nucleolus/*metabolism
DNA-Binding Proteins/*metabolism
Gene Deletion
Gene Expression Regulation; Viral
Green Fluorescent Proteins
Hela Cells
Humans
Luminescent Proteins/genetics/metabolism
Molecular Sequence Data
Peptides/*metabolism
Protein Precursors/*metabolism
Recombinant Fusion Proteins/metabolism
Research Support; Non-U.S. Gov't
Viral Core Proteins/*metabolism

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