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PMID: 12111420 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

The nucleolus--a gateway to viral infection?

Archives of virology ·Vol. 147 ·No. 6 ·2002-06-00 ·Pages 1077-89

Hiscox JA

Abstract

A number of viruses and viral proteins interact with a dynamic sub-nuclear structure called the nucleolus. The nucleolus is present during interphase in mammalian cells and is the site of ribosome biogenesis, and has been implicated in controlling regulatory processes such as the cell cycle. Viruses interact with the nucleolus and its antigens; viral proteins co-localise with factors such as nucleolin, B23 and fibrillarin, and can cause their redistribution during infection. Viruses can use these components as part of their replication process, and also use the nucleolus as a site of replication itself. Many of these properties are not restricted to any particular type of virus or replication mechanism, and examples of these processes can be found in DNA, RNA and retroviruses. Evidence suggests that viruses may target the nucleolus and its components to favour viral transcription, translation and perhaps alter the cell cycle in order to promote virus replication. Autoimmunity to nucleolin and fibrillarin have been associated with a number of diseases, and by targeting the nucleolus and displacing nucleolar antigens, virus infection might play a role in the initiation of these conditions.

MeSH Terms
Amino Acid Sequence Animals Cattle Cell Nucleolus/virology Humans Molecular Sequence Data Viral Proteins/chemistry,metabolism Virus Diseases/physiopathology,virology Virus Physiological Phenomena Viruses/metabolism
Chemicals
Viral Proteins
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Hiscox J A
School of Animal and Microbial Sciences, University of Reading, UK. j.a.hiscox@reading.ac.uk
Article Info
Journal
Archives of virology
Abbr.
Arch Virol
ISSN
0304-8608
Published
2002-06-00
Pages
1077-89
Language
English
Region
Austria
NLM ID
7506870
PMCID
PMC7087241
Subset
IM
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