Abstract
Rat thyroid differentiated cells (PC Cl 3) are an excellent model system with which to study the interaction between differentiation and cell transformation. We previously demonstrated that PC Cl 3 cells expressing the adenovirus E1A gene no longer depend on thyrotropin for growth and do not express thyroid differentiation markers. Here we show that an E1A mutant unable to bind the RB protein failed to transform the PC Cl 3 cells. Conversely, mutations in the E1A p300 interacting region did not affect its transforming ability. The pivotal role of RB family proteins in the thyroid cell transformation is supported by the thyrotropin independence induced by the E7 gene of human papilloma virus type 16, but not by a mutated form in the RB-binding region.
Copyright 2000 Academic Press.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adenovirus E1A Proteins / genetics*
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Animals
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Carrier Proteins*
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Cell Cycle Proteins*
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Cell Differentiation
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Cell Division
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Cell Line
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Cell Transformation, Neoplastic*
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DNA-Binding Proteins*
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E2F Transcription Factors
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Flow Cytometry / methods
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Humans
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Oncogene Proteins, Viral / genetics
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Papillomaviridae / genetics
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Papillomavirus E7 Proteins
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Phenotype
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Rats
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Rats, Inbred F344
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Retinoblastoma Protein / metabolism*
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Retinoblastoma-Binding Protein 1
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Thyroid Gland / cytology
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Thyrotropin / metabolism
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Transcription Factor DP1
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Transcription Factors / genetics
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Transcription Factors / physiology
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Transfection
Substances
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Adenovirus E1A Proteins
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Carrier Proteins
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Cell Cycle Proteins
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DNA-Binding Proteins
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E2F Transcription Factors
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Oncogene Proteins, Viral
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Papillomavirus E7 Proteins
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Retinoblastoma Protein
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Retinoblastoma-Binding Protein 1
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Transcription Factor DP1
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Transcription Factors
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oncogene protein E7, Human papillomavirus type 16
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Thyrotropin