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

被引:30
作者
Chadwick, DR [1 ]
Lever, AML [1 ]
机构
[1] Univ Cambridge, Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, England
基金
英国医学研究理事会;
关键词
HIV; antisense RNA; post-transcriptional;
D O I
10.1038/sj.gt.3301254
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 (psi) region were stably expressed from the CMV IE promoter in Jurkat cells, and expression confirmed by RT-PCR. When challenged with HIV-II cell lines expressing antisense RNA targeting the SD/psi region showed significant inhibition of replication (at up to 10(6) TCID 50/ml). These sequences were also expressed in lymphocytes after transduction using recombinant retroviruses and one sequence complementary to the SD/psi 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 psi 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 (psi) 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.
引用
收藏
页码:1362 / 1368
页数:7
相关论文
共 27 条
[11]   GENE-THERAPY FOR HIV-INFECTION [J].
LEVER, AML .
BRITISH MEDICAL BULLETIN, 1995, 51 (01) :149-166
[12]   The human immunodeficiency virus type 1 encapsidation site is a multipartite RNA element composed of functional hairpin structures [J].
McBride, MS ;
Panganiban, AT .
JOURNAL OF VIROLOGY, 1996, 70 (05) :2963-2973
[13]  
Morgan RA, 1997, CLIN EXP IMMUNOL, V107, P41
[14]   ADVANCED MAMMALIAN GENE-TRANSFER - HIGH TITER RETROVIRAL VECTORS WITH MULTIPLE-DRUG SELECTION MARKERS AND A COMPLEMENTARY HELPER-FREE PACKAGING CELL-LINE [J].
MORGENSTERN, JP ;
LAND, H .
NUCLEIC ACIDS RESEARCH, 1990, 18 (12) :3587-3596
[15]   Long-term protection against HIV-1 infection conferred by tat or rev antisense RNA was affected by the design of the retroviral vector [J].
Peng, HR ;
Callison, D ;
Li, P ;
Burrell, C .
VIROLOGY, 1996, 220 (02) :377-389
[16]   HELPER VIRUS-FREE TRANSFER OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 VECTORS [J].
RICHARDSON, JH ;
KAYE, JF ;
CHILD, LA ;
LEVER, AML .
JOURNAL OF GENERAL VIROLOGY, 1995, 76 :691-696
[17]   T-cell mediated rejection of gene-modified HIV-specific cytotoxic T lymphocytes in HIV-infected patients [J].
Riddell, SR ;
Elliott, M ;
Lewinsohn, DA ;
Gilbert, MJ ;
Wilson, L ;
Manley, SA ;
Lupton, SD ;
Overell, RW ;
Reynolds, TC ;
Corey, L ;
Greenberg, PD .
NATURE MEDICINE, 1996, 2 (02) :216-223
[18]   INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REPLICATION IN HUMAN T-CELLS STABLY EXPRESSING ANTISENSE RNA [J].
SCZAKIEL, G ;
PAWLITA, M .
JOURNAL OF VIROLOGY, 1991, 65 (01) :468-472
[19]  
STEFFENS DL, 1989, BIOTECHNIQUES, V7, P674
[20]   RESISTANCE TO HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INFECTION CONFERRED BY TRANSDUCTION OF HUMAN PERIPHERAL-BLOOD LYMPHOCYTES WITH RIBOZYME, ANTISENSE, OR POLYMERIC TRANSACTIVATION RESPONSE ELEMENT CONSTRUCTS [J].
SUN, LQ ;
PYATI, J ;
SMYTHE, J ;
WANG, L ;
MACPHERSON, J ;
GERLACH, W ;
SYMONDS, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7272-7276