Open chromatin structures regulate the efficiencies of pre-RC formation and replication initiation in Epstein-Barr virus

• Published in: The Journal of cell biology Vol. 198; no. 4; pp. 509 - 528
• Main Authors: Papior, Peer, Arteaga-Salas, José M, Günther, Thomas, Grundhoff, Adam, Schepers, Aloys
• Format: Journal Article
• Language: English
• Published: United States Rockefeller University Press 20-08-2012; The Rockefeller University Press
• Subjects: Binding sites; Burkitt Lymphoma - virology; Cell cycle; Cell Line, Tumor; Chromatin; Chromatin - physiology; Chromatin - virology; Deoxyribonucleic acid; DNA; Epstein-Barr virus; Epstein-Barr Virus Infections - virology; Genomics; Herpesvirus 4, Human - genetics; Herpesvirus 4, Human - growth & development; Humans; Origin Recognition Complex - genetics; Virus Replication - genetics; Viruses
• ISSN: 0021-9525; 1540-8140
• DOI: 10.1083/jcb.201109105

Whether or not metazoan replication initiates at random or specific but flexible sites is an unsolved question. The lack of sequence specificity in origin recognition complex (ORC) DNA binding complicates genome-scale chromatin immunoprecipitation (ChIP)-based studies. Epstein-Barr virus (EBV) persists as chromatinized minichromosomes that are replicated by the host replication machinery. We used EBV to investigate the link between zones of pre-replication complex (pre-RC) assembly, replication initiation, and micrococcal nuclease (MNase) sensitivity at different cell cycle stages in a genome-wide fashion. The dyad symmetry element (DS) of EBV's latent origin, a well-established and very efficient pre-RC assembly region, served as an internal control. We identified 64 pre-RC zones that correlate spatially with 57 short nascent strand (SNS) zones. MNase experiments revealed that pre-RC and SNS zones were linked to regions of increased MNase sensitivity, which is a marker of origin strength. Interestingly, although spatially correlated, pre-RC and SNS zones were characterized by different features. We propose that pre-RCs are formed at flexible but distinct sites, from which only a few are activated per single genome and cell cycle.