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HIV genome transcription induced by polyoma virus middle T antigen through both enhancer- and promoter-dependent LTR activation.

作者信息

Jacqué J M, Vlach J, Virelizier J L, Garcia A

机构信息

Unité d'immunologie virale, Institut Pasteur, Paris, France.

出版信息

C R Acad Sci III. 1995 Dec;318(12):1227-32.

PMID:8745637
Abstract

In order to understand the regulation of HIV genome transcription induced by cell stimulation through transmembrane receptors, we have transfected cells with polyoma middle T antigen (PyMT) expression vectors, thus mimicking activated receptor-dependent cell stimulation. PyMT-expressing Cos7 cells provided an environment where transcription of an HIV provirus was activated. PyMT expression induced the activity of both enhancer- and promoter-dependent HIV-LTR luciferase vectors. Induction of the HIV promoter domain depended on Sp1-binding sites and could be blocked by Wortmannin, an inhibitor of phosphatidylinositol 3-kinase (PI3K). This indicates that PyMT-induced HIV transcription and replication are controlled by both the enhancer and promoter domains of the HIV-LTR. The latter, but not the former, was induced in a PI3K-dependent way. Thus at least 2 different transduction pathways appear to collaborate for induction of full HIV genome transcription in activated cells.

摘要

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