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Parvovirus induced alterations in nuclear architecture and dynamics

Authors :
Teemu O. Ihalainen
Outi Paloheimo
Jussi Timonen
Nicolas Dross
Hanna Smolander
Jörg Langowski
Einari A. Niskanen
Juulia Jylhävä
Maija Vihinen-Ranta
University of Tampere
Source :
PLoS ONE, PLoS ONE, Vol 4, Iss 6, p e5948 (2009)
Publication Year :
2009

Abstract

The nucleus of interphase eukaryotic cell is a highly compartmentalized structure containing the three-dimensional network of chromatin and numerous proteinaceous subcompartments. DNA viruses induce profound changes in the intranuclear structures of their host cells. We are applying a combination of confocal imaging including photobleaching microscopy and computational methods to analyze the modifications of nuclear architecture and dynamics in parvovirus infected cells. Upon canine parvovirus infection, expansion of the viral replication compartment is accompanied by chromatin marginalization to the vicinity of the nuclear membrane. Dextran microinjection and fluorescence recovery after photobleaching (FRAP) studies revealed the homogeneity of this compartment. Markedly, in spite of increase in viral DNA content of the nucleus, a significant increase in the protein mobility was observed in infected compared to non-infected cells. Moreover, analyzis of the dynamics of photoactivable capsid protein demonstrated rapid intranuclear dynamics of viral capsids. Finally, quantitative FRAP and cellular modelling were used to determine the duration of viral genome replication. Altogether, our findings indicate that parvoviruses modify the nuclear structure and dynamics extensively. Intranuclear crowding of viral components leads to enlargement of the interchromosomal domain and to chromatin marginalization via depletion attraction. In conclusion, parvoviruses provide a useful model system for understanding the mechanisms of virus-induced intranuclear modifications. Public Library of Science

Details

ISSN :
19326203
Volume :
4
Issue :
6
Database :
OpenAIRE
Journal :
PloS one
Accession number :
edsair.doi.dedup.....38486b727102835ee34565c183def588