Affiliation:
1. INSERM U649, CHU Hôtel Dieu, Nantes, France
2. Etablissement Français du Sang des Pays de la Loire, Nantes, France
Abstract
ABSTRACT
The p5 promoter region of adeno-associated virus type 2 (AAV-2) is a multifunctional element involved in
rep
gene expression, Rep-dependent replication, and site-specific integration. We initially characterized a 350-bp p5 region by its ability to behave like a
cis
-acting replication element in the presence of Rep proteins and adenoviral factors. The objective of this study was to define the minimal elements within the p5 region required for Rep-dependent replication. Assays performed in transfected cells (in vivo) indicated that the minimal p5 element was composed by a 55-bp sequence (nucleotides 250 to 304 of wild-type AAV-2) containing the TATA box, the Rep binding site, the terminal resolution site present at the transcription initiation site (trs
+1
), and a downstream 17-bp region that could potentially form a hairpin structure localizing the trs
+1
at the top of the loop. Interestingly, the TATA box was absolutely required for in vivo but dispensable for in vitro, i.e., cell-free, replication. We also demonstrated that Rep binding and nicking at the trs
+1
was enhanced in the presence of the cellular TATA binding protein, and that overexpression of this cellular factor increased in vivo replication of the minimal p5 element. Together, these studies identified the minimal replication origin present within the AAV-2 p5 promoter region and demonstrated for the first time the involvement of the TATA box, in
cis
, and of the TATA binding protein, in
trans
, for Rep-dependent replication of this viral element.
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
Cited by
19 articles.
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