Antoni B A, Rabson A B, Miller I L, Trempe J P, Chejanovsky N, Carter B J
Laboratory of Molecular and Cellular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
J Virol. 1991 Jan;65(1):396-404. doi: 10.1128/JVI.65.1.396-404.1991.
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. rep 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.
腺相关病毒(AAV)的rep基因编码AAV DNA复制和AAV基因调控所需的四种蛋白质(Rep78、Rep68、Rep52和Rep40)。此外,Rep蛋白可能在异源系统中具有多效性调节作用,特别是Rep78可能介导负调节作用。我们分析了AAV rep基因对1型人类免疫缺陷病毒(HIV-1)基因表达的影响。2型腺相关病毒(AAV2)的rep基因蛋白抑制了HIV-1的反式激活能力。当与含有HIV-1 tat基因的质粒(pARtat)共转染时,含有AAV2 rep基因(pHIVrep)或从5' HIV-1长末端重复序列表达的CAT基因(pBennCAT)的构建体分别可诱导Rep78和Rep68或CAT表达。当等量的pHIVrep和pBennCAT与越来越多的pARtat共转染时,CAT活性的表达降低。pHIVrep构建体比从野生型AAV2 p5转录启动子表达rep的质粒更具抑制性。通过逆转录酶活性和p24蛋白水平测量,pHIVrep中的rep表达几乎完全抑制了HIV-1前病毒克隆的复制。在转录水平也观察到Rep蛋白对HIV-1产生的抑制作用,即当存在pHIVrep时,所有HIV-1转录本均减少。pHIVrep的抑制作用似乎主要由Rep78介导,也许还有Rep68。这些结果表明,来自异源病毒的反式作用蛋白可能用于抑制HIV-1的生长。