Complex formation of human papillomavirus E7 proteins with the retinoblastoma tumor suppressor gene product - PubMed (original) (raw)
Comparative Study
Complex formation of human papillomavirus E7 proteins with the retinoblastoma tumor suppressor gene product
K Münger et al. EMBO J. 1989.
Abstract
The E7 proteins encoded by the human papillomaviruses (HPVs) associated with anogenital lesions share significant amino acid sequence homology. The E7 proteins of these different HPVs were assessed for their ability to form complexes with the retinoblastoma tumor suppressor gene product (p105-RB). Similar to the E7 protein of HPV-16, the E7 proteins of HPV-18, HBV-6b and HPV-11 were found to associate with p105-RB in vitro. The E7 proteins of HPV types associated with a high risk of malignant progression (HPV-16 and HPV-18) formed complexes with p105-RB with equal affinities. The E7 proteins encoded by HPV types 6b and 11, which are associated with clinical lesions with a lower risk for progression, bound to p105-RB with lower affinities. The E7 protein of the bovine papillomavirus type 1 (BPV-1), which does not share structural similarity in the amino terminal region with the HPV E7 proteins, was unable to form a detectable complex with p105-RB. The amino acid sequences of the HPV-16 E7 protein involved in complex formation with p105-RB in vitro have been mapped. Only a portion of the sequences that are conserved between the HPV E7 proteins and AdE1A were necessary for association with p105-RB. Furthermore, the HPV-16 E7-p105-RB complex was detected in an HPV-16-transformed human keratinocyte cell line.
Similar articles
- The E7 proteins of the nononcogenic human papillomavirus type 6b (HPV-6b) and of the oncogenic HPV-16 differ in retinoblastoma protein binding and other properties.
Gage JR, Meyers C, Wettstein FO. Gage JR, et al. J Virol. 1990 Feb;64(2):723-30. doi: 10.1128/JVI.64.2.723-730.1990. J Virol. 1990. PMID: 2153238 Free PMC article. - The human papilloma virus-16 E7 oncoprotein is able to bind to the retinoblastoma gene product.
Dyson N, Howley PM, Münger K, Harlow E. Dyson N, et al. Science. 1989 Feb 17;243(4893):934-7. doi: 10.1126/science.2537532. Science. 1989. PMID: 2537532 - Molecular mechanisms of transformation by the human papillomaviruses.
Howley PM, Münger K, Werness BA, Phelps WC, Schlegel R. Howley PM, et al. Princess Takamatsu Symp. 1989;20:199-206. Princess Takamatsu Symp. 1989. PMID: 2562182 Review. - Cellular targets of the oncoproteins encoded by the cancer associated human papillomaviruses.
Howley PM, Münger K, Romanczuk H, Scheffner M, Huibregtse JM. Howley PM, et al. Princess Takamatsu Symp. 1991;22:239-48. Princess Takamatsu Symp. 1991. PMID: 1668886 Review.
Cited by
- The Hallmarks of Cervical Cancer: Molecular Mechanisms Induced by Human Papillomavirus.
Rosendo-Chalma P, Antonio-Véjar V, Ortiz Tejedor JG, Ortiz Segarra J, Vega Crespo B, Bigoni-Ordóñez GD. Rosendo-Chalma P, et al. Biology (Basel). 2024 Jan 27;13(2):77. doi: 10.3390/biology13020077. Biology (Basel). 2024. PMID: 38392296 Free PMC article. Review. - A cellular protein mediates association of p53 with the E6 oncoprotein of human papillomavirus types 16 or 18.
Huibregtse JM, Scheffner M, Howley PM. Huibregtse JM, et al. EMBO J. 1991 Dec;10(13):4129-35. doi: 10.1002/j.1460-2075.1991.tb04990.x. EMBO J. 1991. PMID: 1661671 Free PMC article. - Modulation of immortalizing properties of human papillomavirus type 16 E7 by p53 expression.
Crook T, Fisher C, Vousden KH. Crook T, et al. J Virol. 1991 Jan;65(1):505-10. doi: 10.1128/JVI.65.1.505-510.1991. J Virol. 1991. PMID: 1845904 Free PMC article. - Murine coronavirus nonstructural protein p28 arrests cell cycle in G0/G1 phase.
Chen CJ, Sugiyama K, Kubo H, Huang C, Makino S. Chen CJ, et al. J Virol. 2004 Oct;78(19):10410-9. doi: 10.1128/JVI.78.19.10410-10419.2004. J Virol. 2004. PMID: 15367607 Free PMC article. - Degradation of p53, not telomerase activation, by E6 is required for bypass of crisis and immortalization by human papillomavirus type 16 E6/E7.
McMurray HR, McCance DJ. McMurray HR, et al. J Virol. 2004 Jun;78(11):5698-706. doi: 10.1128/JVI.78.11.5698-5706.2004. J Virol. 2004. PMID: 15140967 Free PMC article.
References
- Nature. 1979 Mar 15;278(5701):261-3 - PubMed
- Virology. 1984 Nov;139(1):109-37 - PubMed
- J Virol. 1980 Apr;34(1):213-24 - PubMed
- J Virol. 1981 Sep;39(3):861-9 - PubMed
- Cell. 1982 Feb;28(2):387-94 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical