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Essential role for p53-mediated transcription in E1A-induced apoptosis.

Open access
Sabbatini, P, Lin, J, Levine, A J, White, E·1995·Genes & Development

Abstract

Baby rat kidney (BRK) cell lines transformed by E1A and a temperature-sensitive p53 [tsp53(val135)] undergo rapid apoptosis when p53 assumes the wild-type conformation at the permissive temperature. Wild-type p53 function is therefore required for induction of apoptosis in response to growth deregulation by E1A. BRK cells transformed by E1A and a transcriptionally defective temperature-sensitive p53 [tsp53(22-23val135)] are dramatically impaired for the ability to mediate E1A-induced apoptosis at the permissive temperature. The tsp53(22-23val135), however, still retains some ability to suppress cell growth. Thus, the activity of p53 as a transcription factor is directly correlated with the ability of E1A to induce apoptosis. In addition, there may exist at least two different mechanisms by which p53 can suppress cell-cycle progression, only one of which is dependent on p53-mediated transcription.

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Metadata

Authors
Sabbatini, P., Lin, J., Levine, A. J., & White, E.
Venue
Genes & Development
Published
1995-09-01
Volume
9
Issue
17
Pages
2184-2192
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W1972376460
Cited by
215
References
4
Type
posted content
Language
en
Open access
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CoChat. (2026). Citation check: Essential role for p53-mediated transcription in E1A-induced apoptosis. https://app.cochat.ai/papers/10.1101/gad.9.17.2184
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Sabbatini, P., Lin, J., Levine, A. J., & White, E. (1995). Essential role for p53-mediated transcription in E1A-induced apoptosis. Genes & Development. https://doi.org/10.1101/gad.9.17.2184

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