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人类免疫缺陷病毒1型env基因序列对于鼠巨细胞病毒主要立即早期启动子的Tat蛋白进行不依赖TAR的反式激活的需求。

Requirement of the human immunodeficiency virus type 1 env gene sequence for TAR-independent trans activation by Tat from the major immediate-early promoter of murine cytomegalovirus.

作者信息

Kim Y S

机构信息

McArdle Laboratory for Cancer Research, University of Wisconsin, Madison, 53706.

出版信息

Biochem Biophys Res Commun. 1994 Sep 15;203(2):1152-9. doi: 10.1006/bbrc.1994.2303.

Abstract

Previously it has been demonstrated that the human immunodeficiency virus type 1 (HIV-1) Tat protein mediates induction of the HIV-1 env expression through a TAR-independent manner in heterologous and homologous promoter systems (Kim and Risser, 1993, J. Virol. 67, 239; Kim and Panganiban, 1993, J. Virol. 67, 3739). To further explore the transactivation of HIV-1 env gene, I examined expression of the env, the bacterial CAT, and the firefly luciferase genes from a heterologous promoter, the major immediate-early promoter (MIEP) of murine cytomegalovirus (MCMV). Here we show that Tat augments gene expression from the MCMV MIEP only when linked to the env gene. Surprisingly, in contrast to the expression from an HIV-1 LTR lacking the TAR element, TAR-independent transactivation of env gene expression from MCMV MIEP did not require the full length Tat protein. In addition, deletion of the previously identified cis-acting Tat-responsive element in env did not affect Tat transactivation of the env gene expression. Thus, there are multiple distinct elements that mediate Tat responsiveness in the absence TAR.

摘要

先前已证明,在异源和同源启动子系统中,人类免疫缺陷病毒1型(HIV-1)Tat蛋白通过不依赖TAR的方式介导HIV-1 env表达的诱导(Kim和Risser,1993年,《病毒学杂志》67卷,239页;Kim和Panganiban,1993年,《病毒学杂志》67卷,3739页)。为了进一步探究HIV-1 env基因的反式激活作用,我检测了来自异源启动子——鼠巨细胞病毒(MCMV)的主要立即早期启动子(MIEP)的env、细菌氯霉素乙酰转移酶(CAT)和萤火虫荧光素酶基因的表达。我们在此表明,Tat仅在与env基因相连时才增强来自MCMV MIEP的基因表达。令人惊讶的是,与缺乏TAR元件的HIV-1长末端重复序列(LTR)的表达相反,来自MCMV MIEP的env基因表达的不依赖TAR的反式激活并不需要全长Tat蛋白。此外,缺失env中先前鉴定的顺式作用Tat反应元件并不影响Tat对env基因表达的反式激活。因此,在没有TAR的情况下,有多个不同的元件介导Tat反应性。

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