Transforming activities of JC virus early proteins.
Journal
  Advances in experimental medicine and biology.
Citation
  Adv Exp Med Biol. 577:288-309
Publication date
  2006
Authors
  Frisque RJ
Hofstetter C
Tyagarajan SK
Investigators
  Richard Frisque
Grant agencies
  National Institute of Neurological Disorders and Stroke
Grants
  NINDS NS41833
Abstract
  Polyomaviruses, as their name indicates, are viruses capable of inducing a variety of tumors in vivo. Members of this family, including the human JC and BK viruses (JCV, BKV), and the better characterized mouse polyomavirus and simian virus 40 (SV40), are small DNA viruses that commandeer a cell's molecular machinery to reproduce themselves. Studies of these virus-host interactions have greatly enhanced our understanding of a wide range of phenomena from cellular processes (e.g., DNA replication and transcription) to viral oncogenesis. The current chapter will focus upon the five known JCV early proteins and the contributions each makes to the oncogenic process (transformation) when expressed in cultured cells. Where appropriate, gaps in our understanding of JCV protein function will be supplanted with information obtained from the study of SV40 and BKV.
Medline ID
  102921915