Abstract

Inside the adenovirus virion, the genome forms a chromatin-like structure with viral basic core proteins. Core protein VII is the major DNA binding protein and was shown to remain associated with viral genomes upon virus entry even after nuclear delivery. It has been suggested that protein VII plays a regulatory role in viral gene expression and is a functional component of viral chromatin complexes in host cells. As such, protein VII could be used as a maker to track adenoviral chromatin complexes in vivo. In this study, we characterize a new monoclonal antibody against protein VII that stains incoming viral chromatin complexes following nuclear import. Furthermore, we describe the development of a novel imaging system that uses Template Activating Factor-I (TAF-I/SET), a cellular chromatin protein tightly bound to protein VII upon infection. This setup allows us not only to rapidly visualize protein VII foci in fixed cells but also to monitor their movement in living cells. These powerful tools can provide novel insights into the spatio-temporal regulation of incoming adenoviral chromatin complexes.

Highlights

  • Adenovirus (Ad) is a non-enveloped virus with a linear double-stranded DNA genome

  • Protein VII is thought to largely remain associated with the viral genome, at least during the first hours of infection, how long this association lasts is subject to debate [3]

  • Genome association after nuclear import is supported by several biochemical assays [4], including chromatin immunoprecipitation (ChIP) assays [5,6,7,8], and microscopy

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Summary

Introduction

Adenovirus (Ad) is a non-enveloped virus with a linear double-stranded DNA genome. The Ad genome forms a chromatin-like structure with viral basic core proteins, protein V, VII, and polypeptide X/mu [1]. Protein VII is thought to largely remain associated with the viral genome, at least during the first hours of infection (including its nuclear import), how long this association lasts is subject to debate [3]. Genome association after nuclear import is supported by several biochemical assays [4], including chromatin immunoprecipitation (ChIP) assays [5,6,7,8], and microscopy (see below). We have reported using reconstituted protein VII-DNA complexes that

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