Genetic requirements for the episomal maintenance of oncogenic herpesvirus genomes.

Adv Cancer Res

Department of Medical Microbiology and Immunology and the H. Lee Moffitt Cancer Center, University of South Florida, Tampa 33612-4799, USA.

Published: August 2002

AI Article Synopsis

  • Herpesviruses are large double-stranded DNA viruses that can remain latent in the body for life.
  • Epstein-Barr virus (EBV), Kaposi's sarcoma-associated herpesvirus (KSHV), and simian herpesvirus saimiri (HVS) are linked to serious illnesses like malignant lymphoproliferative diseases.
  • During latency, these viruses express few genes and their DNA exists as a stable, circular episome that integrates with host chromosomes, ensuring the virus's long-term survival.

Article Abstract

Herpesviruses are large double-stranded DNA viruses that are characterized by lifelong latency. Epstein-Barr virus (EBV), the recently discovered Kaposi's sarcoma associated herpesvirus (KSHV), also referred to as human herpesvirus-8 (HHV-8), and the simian Herpesvirus saimiri (HVS) are associated with malignant lymphoproliferative diseases. These viruses establish latent infection in lymphoid cells. During latency only a few viral genes are expressed and the viral genome persists as a multicopy circular episome. The episome contains repetitive sequences that serve as multiple cooperative binding sites for the viral DNA binding proteins Epstein-Barr virus nuclear antigen 1 (EBNA-1) of EBV and latency-associated nuclear antigen (LANA1) of KSHV and HVS, which are expressed during latency. The oligomerized proteins associate with the viral genome and tether it to host chromosomes, assuring continual lifelong persistence of the virus.

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Source
http://dx.doi.org/10.1016/s0065-230x(02)84005-2DOI Listing

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