Natural Biology of Polyomavirus Middle T Antigen
Open Access
- 1 June 2001
- journal article
- review article
- Published by American Society for Microbiology in Microbiology and Molecular Biology Reviews
- Vol. 65 (2), 288-318
- https://doi.org/10.1128/mmbr.65.2.288-318.2001
Abstract
“It has been commented by someone that ‘polyoma’ is an adjective composed of a prefix and suffix, with no root between—a meatless linguistic sandwich” (C. J. Dawe). The very name “polyomavirus” is a vague mantel: a name given before our understanding of these viral agents was clear but implying a clear tumor life-style, as noted by the late C. J. Dawe. However, polyomavirus are not by nature tumor-inducing agents. Since it is the purpose of this review to consider the natural function of middle T antigen (MT), encoded by one of the seemingly crucial transforming genes of polyomavirus, we will reconsider and redefine the virus and its MT gene in the context of its natural biology and function. This review was motivated by our recent in vivo analysis of MT function. Using intranasal inoculation of adult SCID mice, we have shown that polyomavirus can replicate with an MT lacking all functions associated with transformation to similar levels to wild-type virus. These observations, along with an almost indistinguishable replication of all MT mutants with respect to wild-type viruses in adult competent mice, illustrate that MT can have a play subtle role in acute replication and persistence. The most notable effect of MT mutants was in infections of newborns, indicating that polyomavirus may be highly adapted to replication in newborn lungs. It is from this context that our current understanding of this well-studied virus and gene is presented.Keywords
This publication has 422 references indexed in Scilit:
- Ribosomal S6 Kinase Signaling and the Control of TranslationExperimental Cell Research, 1999
- Stimulation of Membrane Ruffling and MAP Kinase Activation by Distinct Effectors of RASScience, 1996
- Activation and Nuclear Translocation of Mitogen-activated Protein Kinases by Polyomavirus Middle-T or Serum Depend on Phosphatidylinositol 3-KinasePublished by Elsevier ,1995
- Transcriptional Regulation of the PCNA Promoter by p53Biochemical and Biophysical Research Communications, 1994
- Phosphatidylinositol-3-OH kinase direct target of RasNature, 1994
- Endothelial cell transformation by polyomavirus middle T antigen in mice lacking Src-related kinasesCurrent Biology, 1994
- The murine p53 protein blocks replication of SV40 DNA in vitro by inhibiting the initiation functions of SV40 large T antigenCell, 1989
- Endothelial cell tumors develop in transgenic mice carrying polyoma virus middle T oncogeneCell, 1987
- An 81 kd protein complexed with middle T antigen and pp60c-src: A possible phosphatidylinositol kinaseCell, 1987
- Enhancement of cellular src gene product associated tyrosyl kinase activity following polyoma virus infection and transformationCell, 1984