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ABSTRACT Antisense RNA has proven a potent inhibitor of gene expression and has the potential to inhibit retroviral replication at a number of stages in the virus life cycle by targeting
both viral and cellular RNA sequences. Antisense RNA complementary to three target regions in the 5′ leader/LTR of human immunodeficiency virus type-1 (HIV-1), the TAR region, the primer
binding site and the splice donor (SD)-packaging signal (ψ) region were stably expressed from the CMV IE promoter in Jurkat cells, and expression confirmed by RT-PCR. When challenged with
HIV-1, cell lines expressing antisense RNA targeting the SD/ψ region showed significant inhibition of replication (at up to 106 TCID 50/ml). These sequences were also expressed in
lymphocytes after transduction using recombinant retroviruses and one sequence complementary to the SD/ψ region inhibited replication of HIV-1. A co-transfection assay using COS-1 cells was
also developed both to confirm the antiviral potential of these sequences, and to determine the predominant site of action of these molecules. Antisense RNAs targeting the ψ region and one
sequence complementary to the TAR region inhibited expression of viral protein; furthermore, analyses of relative levels of cellular and virion RNA from these assays suggest each of these
antisense molecules exerts its effect at an early stage in the transcription–translation pathway, while the longer of the sequences also inhibited packaging of virion RNA. These results
suggest that the packaging signal (ψ) of HIV-1 represents an attractive target for antisense RNA-based gene therapy, although the main mode of action of such molecules may well be through
antisense effects at an earlier stage of replication than packaging. Access through your institution Buy or subscribe This is a preview of subscription content, access via your institution
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about institutional subscriptions * Read our FAQs * Contact customer support SIMILAR CONTENT BEING VIEWED BY OTHERS EVIDENCE THAT TWO INSTEAD OF ONE DEFECTIVE INTERFERING RNA IN INFLUENZA A
VIRUS-DERIVED DEFECTIVE INTERFERING PARTICLES (DIPS) DOES NOT ENHANCE ANTIVIRAL ACTIVITY Article Open access 14 October 2021 CHEMOGENETIC ON AND OFF SWITCHES FOR RNA VIRUS REPLICATION
Article Open access 01 March 2021 1MΨ INFLUENCES THE PERFORMANCE OF VARIOUS POSITIVE-STRANDED RNA VIRUS-BASED REPLICONS Article Open access 31 July 2024 REFERENCES * Lever AML . Gene therapy
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supported by a MRC Clinical Training Fellowship (DC): G84/4391 and the Sykes Trust. AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Department of Medicine, University of Cambridge,
Addenbrooke's Hospital, Cambridge, CB2 2QQ, UK D R Chadwick & A M L Lever Authors * D R Chadwick View author publications You can also search for this author inPubMed Google Scholar
* A M L Lever View author publications You can also search for this author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE
Chadwick, D., Lever, A. Antisense RNA sequences targeting the 5′ leader packaging signal region of human immunodeficiency virus type-1 inhibits viral replication at post-transcriptional
stages of the life cycle. _Gene Ther_ 7, 1362–1368 (2000). https://doi.org/10.1038/sj.gt.3301254 Download citation * Received: 28 February 2000 * Accepted: 03 May 2000 * Published: 21 August
2000 * Issue Date: 01 August 2000 * DOI: https://doi.org/10.1038/sj.gt.3301254 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable
link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative KEYWORDS * HIV * antisense RNA
* post-transcriptional