Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2006-4-13
pubmed:abstractText
A common feature associated with the replication of most RNA viruses is the formation of a unique membrane environment encapsulating the viral replication complex. For their part, flaviviruses are no exception, whereupon infection causes a dramatic rearrangement and induction of unique membrane structures within the cytoplasm of infected cells. These virus-induced membranes, termed paracrystalline arrays, convoluted membranes, and vesicle packets, all appear to have specific functions during replication and are derived from different organelles within the host cell. The aim of this study was to identify which protein(s) specified by the Australian strain of West Nile virus, Kunjin virus (KUNV), are responsible for the dramatic membrane alterations observed during infection. Thus, we have shown using immunolabeling of ultrathin cryosections of transfected cells that expression of the KUNV polyprotein intermediates NS4A-4B and NS2B-3-4A, as well as that of individual NS4A proteins with and without the C-terminal transmembrane domain 2K, resulted in different degrees of rearrangement of cytoplasmic membranes. The formation of the membrane structures characteristic for virus infection required coexpression of an NS4A-NS4B cassette with the viral protease NS2B-3pro which was shown to be essential for the release of the individual NS4A and NS4B proteins. Individual expression of NS4A protein retaining the C-terminal transmembrane domain 2K resulted in the induction of membrane rearrangements most resembling virus-induced structures, while removal of the 2K domain led to a less profound membrane rearrangement but resulted in the redistribution of the NS4A protein to the Golgi apparatus. The results show that cleavage of the KUNV polyprotein NS4A-4B by the viral protease is the key initiation event in the induction of membrane rearrangement and that the NS4A protein intermediate containing the uncleaved C-terminal transmembrane domain plays an essential role in these membrane rearrangements.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-10438855, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-10482557, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-10516064, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-10590087, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-11145899, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-11352669, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-11602720, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-12021330, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-12082996, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-12368353, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-12829824, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-1322651, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-1328486, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-14671099, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-14696328, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-15084397, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-1531368, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-15831953, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-15956546, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-1597508, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-16190978, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-1683727, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-2541547, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-2820130, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-2826659, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-2904446, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-3029292, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-7691276, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-8207832, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-8445732, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-8659120, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-8690769, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-8794292, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-8971020, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-9234944, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-9261387, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-9448689, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-9499070, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-9621059, http://linkedlifedata.com/resource/pubmed/commentcorrection/16611922-9636360
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0022-538X
pubmed:author
pubmed:issnType
Print
pubmed:volume
80
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4623-32
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
2006
pubmed:articleTitle
Regulated cleavages at the West Nile virus NS4A-2K-NS4B junctions play a major role in rearranging cytoplasmic membranes and Golgi trafficking of the NS4A protein.
pubmed:affiliation
School of Molecular and Microbial Sciences, University of Queensland, Coopers Road, St. Lucia, Brisbane, Queensland 4072, Australia.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't