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Intranuclear localization of human papillomavirus 16 E7 during transformation and preferential binding of E7 to the Rb family member p130
Abstract
To study intracellular pathways by which the human papillomavirus 16 oncogene E7 participates in carcinogenesis, we expressed an inducible chimera of E7 by fusion to the hormone-binding domain of the estrogen receptor. The chimeric protein (E7ER) transformed rodent fibroblast cell lines and induced DNA synthesis on addition of estradiol. In coimmunoprecipitation experiments, E7ER preferentially bound p130 when compared to p107 and pRb. After estradiol addition, E7ER localization changed to a more intense intranuclear staining. Induction of E7 function was not correlated with binding to p130 or pRb but rather with intranuclear localization and modest induction of binding to p107.
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“HPV-16 E7 was shown to be a cytoplasmic phosphoprotein as early as 1987 [72]; however, nuclear pools have also been reported [73,74,75,76]”
From The Not-So-Good, the Bad and the Ugly: HPV E5, E6 and E7 Oncoproteins in the Orchestration of Carcinogenesis (2021) · cites this paper as [76]
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Cited by
Targeted disruption of the three Rb-related genes leads to loss of G 1 control and immortalization
Sage, J., Mulligan, G. J., Attardi, L. D., Miller, A., Chen, S., Williams, B., Theodorou, E., & Jacks, T. (2000) · Genes & Development · doi:10.1101/gad.843200 · Cited by 582
Basukala, O., & Banks, L. (2021) · Viruses · doi:10.3390/v13101892 · Cited by 137
Metadata
- Authors
- Smith-McCune, K., Kalman, D., Robbins, C., Shivakumar, S., Yuschenkoff, L., & Bishop, J. M.
- Affiliations
- Department of Obstetrics, Gynecology, and Reproductive Sciences, Cancer Research Institute, and Reproductive Endocrinology Center, and G. W. Hooper Foundation and Department of Microbiology and Immunology, University of California, San Francisco CA 94115
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1999-06-08
- Volume
- 96
- Issue
- 12
- Pages
- 6999-7004
- ISSN
- 0027-8424
- 1091-6490
- Cited by
- 49
- References
- 0
- Language
- en
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