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人类免疫缺陷病毒1型反式激活因子蛋白可增强人乳头瘤病毒16型的E2依赖性转录。

The HIV-1 tat protein enhances E2-dependent human papillomavirus 16 transcription.

作者信息

Vernon S D, Hart C E, Reeves W C, Icenogle J P

机构信息

Division of Viral and Rickettsial Diseases, Centers for Disease Control, Atlanta, GA 30333.

出版信息

Virus Res. 1993 Feb;27(2):133-45. doi: 10.1016/0168-1702(93)90077-z.

Abstract

Epidemiologic studies show an association between infection with human immunodeficiency virus type 1 (HIV-1) and human papillomavirus (HPV) associated anogenital disease. To investigate possible molecular mechanisms of HIV-1 modulation of HPV expression, we studied the effect of an HIV-1 regulatory protein, tat1, on gene expression directed by the upstream regulatory region (URR) of HPV type 16 (HPV 16). HPV 16 URR-directed chloramphenicol acetyltransferase (CAT) expression driven by the native HPV 16 promoter (P97) was increased in the presence of tat1 alone. Tat1 also reversed E2-mediated repression of P97-directed CAT expression. E2 mediated CAT expression with URR constructs containing the SV40 promoter was enhanced when tat1 and E2 were cotransfected. Using a cervical carcinoma cell line (SiHa), E2 enhancement of URR-directed gene expression was elevated in the presence of extracellular tat1 or during cocultivation with HIV-1-infected cells. These results show HIV can modulate HPV gene expression in cell culture and that the increased rate of HPV-associated cervical disease in asymptomatic HIV-seropositive women may result from HPV-HIV molecular interactions.

摘要

流行病学研究表明,1型人类免疫缺陷病毒(HIV-1)感染与人类乳头瘤病毒(HPV)相关的肛门生殖器疾病之间存在关联。为了研究HIV-1调节HPV表达的可能分子机制,我们研究了一种HIV-1调节蛋白tat1对16型HPV(HPV 16)上游调节区(URR)指导的基因表达的影响。在仅存在tat1的情况下,由天然HPV 16启动子(P97)驱动的HPV 16 URR指导的氯霉素乙酰转移酶(CAT)表达增加。Tat1还逆转了E2介导的对P97指导的CAT表达的抑制作用。当tat1和E2共转染时,E2与含有SV40启动子的URR构建体介导的CAT表达增强。使用宫颈癌细胞系(SiHa),在存在细胞外tat1的情况下或与HIV-1感染细胞共培养期间,E2对URR指导的基因表达的增强作用升高。这些结果表明,HIV可在细胞培养中调节HPV基因表达,无症状HIV血清阳性女性中HPV相关宫颈疾病发病率的增加可能是由HPV与HIV的分子相互作用所致。

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