אסיף מאגר המחקר החקלאי

Adeno-associated virus Rep protein inhibits human immunodeficiency virus type 1 production in human cells

Year:

1991

Source of publication :

Authors :

Volume :

65

Co-Authors:

Antoni, B.A., Lab. Molecular/Cellular Biol., National Inst. of Diabetes, and Digestive/Kidney Diseases, Bethesda, MD 20892, United States
Rabson, A.B., Lab. Molecular/Cellular Biol., National Inst. of Diabetes, and Digestive/Kidney Diseases, Bethesda, MD 20892, United States
Miller, I.L., Lab. Molecular/Cellular Biol., National Inst. of Diabetes, and Digestive/Kidney Diseases, Bethesda, MD 20892, United States
Trempe, J.P., Lab. Molecular/Cellular Biol., National Inst. of Diabetes, and Digestive/Kidney Diseases, Bethesda, MD 20892, United States
Chejanovsky, N., Lab. Molecular/Cellular Biol., National Inst. of Diabetes, and Digestive/Kidney Diseases, Bethesda, MD 20892, United States
Carter, B.J., Lab. Molecular/Cellular Biol., National Inst. of Diabetes, and Digestive/Kidney Diseases, Bethesda, MD 20892, United States

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Abstract:

The adeno-associated virus (AAV) rep gene encodes four proteins (Rep78, Rep68, Rep52, and Rep40) required for AAV DNA replication and AAV gene regulation. In addition, the Rep proteins may have pleiotropic regulatory effects in heterologous systems, and in particular Rep78 may mediate a negative regulatory effect. We analyzed the effects of the AAV rep gene on human immunodeficiency virus type 1 (HIV-1) gene expression. The rep gene proteins of AAV type 2 (AAV2) inhibited the trans-activating ability of HIV-1. Constructs containing the AAV2 rep gene (pHIVrep) or a CAT gene (pBennCAT) expressed from the 5, HIV-1 long terminal repeat were inducible for Rep78 and Rep68 or CAT expression, respectively, when cotransfected with a plasmid containing the HIV-1 tat gene (pARtat). When equivalent amounts of pHIVrep and pBennCAT were cotransfected with increasing amounts of pARtat, expression of CAT activity was decreased. The pHIVrep construct was more inhibitory than plasmids expressing rep from the wild-type AAV2 p5 transcription promoter. expression from pHIVrep almost completely inhibited the replication of an HIV-1 proviral clone as measured by reverse transcriptase activity and p24 protein levels. Inhibition of HIV-1 production by Rep protein was also seen at the transcriptional level in that all HIV-1 transcripts were decreased when pHIVrep was present. The inhibitory effects of pHIVrep appear to be mediated primarily by Rep78 and perhaps Rep68. These results suggest that a trans-acting protein from a heterologous virus might be used to inhibit HIV-1 growth.

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