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Journal of Virology, December 2001, p. 12058-12069, Vol. 75, No. 24
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.24.12058-12069.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
The Major Human Immunodeficiency Virus Type 2 (HIV-2) Packaging
Signal Is Present on All HIV-2 RNA Species: Cotranslational RNA
Encapsidation and Limitation of Gag Protein Confer
Specificity
Stephen D. C.
Griffin,
Jane F.
Allen,
and
Andrew M. L.
Lever*
Department of Medicine, University of
Cambridge, Addenbrooke's Hospital, Cambridge CB2 2QQ, United Kingdom
Received 23 March 2001/Accepted 3 August 2001
Deletion of a region of the human immunodeficiency virus type 2 (HIV-2) 5' leader RNA reduces genomic RNA encapsidation to about 5%
that of wild-type virus with no defect in viral protein production but
severely limits virus spread in Jurkat T cells, indicating that this
region contains a major cis-acting encapsidation signal,
or psi (
). Being upstream of the major splice donor, it is present
on all viral transcripts. We have shown that HIV-2 selects its genomic
RNA for encapsidation cotranslationally, rendering wild-type HIV-2
unable to encapsidate vector RNAs in trans . Virus with
deleted, however, encapsidates an HIV-2 vector, demonstrating competition for Gag protein. HIV-2 overcomes the lack of packaging signal location specificity by two novel mechanisms, cotranslational packaging and competition for limiting Gag polyprotein.
*
Corresponding author. Mailing address: Department of
Medicine, University of Cambridge, Level 5, Addenbrooke's Hospital,
Hills Rd., Cambridge CB2 2QQ, United Kingdom. Phone: 44-223 336747. Fax: 44-223 336846. E-mail:
amll1{at}mole.bio.cam.ac.uk.

Previously Jane F.
Kaye.
Journal of Virology, December 2001, p. 12058-12069, Vol. 75, No. 24
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.24.12058-12069.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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