Identification of rep-associated factors in herpes simplex virus type 1-induced adeno-associated virus type 2 replication compartments

Autor: Lauriane Kuhn, Armel Nicolas, Anna Salvetti, Coline Biollay, Loredana Arata, Alberto L. Epstein, Nelly Jolinon, Sandra K. Weller, Anna Greco, Nathalie Alazard-Dany, Myriam Ferro
Přispěvatelé: Centre de génétique et de physiologie moléculaire et cellulaire (CGPhiMC), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon, Laboratoire de physiologie cellulaire végétale (LPCV), Université Joseph Fourier - Grenoble 1 (UJF)-Institut National de la Recherche Agronomique (INRA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Biologie à Grande Échelle (BGE - UMR S1038), Institut de Recherche Interdisciplinaire de Grenoble (IRIG), Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Grenoble Alpes (UGA), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Grenoble Alpes [2016-2019] (UGA [2016-2019])-Institut de Recherche Interdisciplinaire de Grenoble (IRIG), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Grenoble Alpes (UGA)-Institut de Recherche Interdisciplinaire de Grenoble (IRIG)
Jazyk: angličtina
Rok vydání: 2010
Předmět:
viruses
MESH: DNA Replication
MESH: Herpes Simplex
Herpesvirus 1
Human

MESH: Dependovirus
medicine.disease_cause
Virus Replication
Replication Protein A
Chlorocebus aethiops
Protein Interaction Mapping
MESH: Animals
Replication Protein C
Adeno-Associated Virus Type 2
0303 health sciences
biology
030302 biochemistry & molecular biology
Dependovirus
Genome Replication and Regulation of Viral Gene Expression
DNA-Binding Proteins
MESH: Herpesvirus 1
Human

Helper virus
DNA mismatch repair
Human
Protein Binding
DNA Replication
Immunology
MESH: Vero Cells
MESH: Parvoviridae Infections
Microbiology
Virus
Cercopithecus aethiops
Parvoviridae Infections
03 medical and health sciences
Viral Proteins
Virology
medicine
Animals
Humans
MESH: Protein Binding
MESH: Replication Protein C
[SDV.BBM]Life Sciences [q-bio]/Biochemistry
Molecular Biology

MESH: Replication Protein A
Vero Cells
030304 developmental biology
MESH: Humans
Herpesvirus 1
MESH: Protein Interaction Mapping
MESH: Virus Replication
DNA replication
Herpes Simplex
MESH: Cercopithecus aethiops
MESH: Viral Proteins
Proliferating cell nuclear antigen
Herpes simplex virus
Viral replication
Insect Science
MESH: HeLa Cells
biology.protein
MESH: DNA-Binding Proteins
HeLa Cells
Zdroj: Journal of Virology
Journal of Virology, American Society for Microbiology, 2010, 84 (17), pp.8871-87. ⟨10.1128/JVI.00725-10⟩
Journal of Virology, 2010, 84 (17), pp.8871-87. ⟨10.1128/JVI.00725-10⟩
ISSN: 0022-538X
1098-5514
DOI: 10.1128/JVI.00725-10⟩
Popis: Adeno-associated virus (AAV) is a human parvovirus that replicates only in cells coinfected with a helper virus, such as adenovirus or herpes simplex virus type 1 (HSV-1). We previously showed that nine HSV-1 factors are able to support AAV rep gene expression and genome replication. To elucidate the strategy of AAV replication in the presence of HSV-1, we undertook a proteomic analysis of cellular and HSV-1 factors associated with Rep proteins and thus potentially recruited within AAV replication compartments (AAV RCs). This study resulted in the identification of approximately 60 cellular proteins, among which factors involved in DNA and RNA metabolism represented the largest functional categories. Validation analyses indicated that the cellular DNA replication enzymes RPA, RFC, and PCNA were recruited within HSV-1-induced AAV RCs. Polymerase δ was not identified but subsequently was shown to colocalize with Rep within AAV RCs even in the presence of the HSV-1 polymerase complex. In addition, we found that AAV replication is associated with the recruitment of components of the Mre11/Rad50/Nbs1 complex, Ku70 and -86, and the mismatch repair proteins MSH2, -3, and -6. Finally, several HSV-1 factors were also found to be associated with Rep, including UL12. We demonstrated for the first time that this protein plays a role during AAV replication by enhancing the resolution of AAV replicative forms and AAV particle production. Altogether, these analyses provide the basis to understand how AAV adapts its replication strategy to the nuclear environment induced by the helper virus.
Databáze: OpenAIRE