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Cited by 342

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

Identification of a minimal transforming domain of p53: negative dominance through abrogation of sequence-specific DNA binding.

Open access
Shaulian, E, Zauberman, A, Ginsberg, D, Oren, M·1992·Molecular and Cellular Biology

Abstract

Mutations in the p53 gene are most frequent in cancer. Many p53 mutants possess transforming activity in vitro. In cells transformed by such mutants, the mutant protein is oligomerized with endogenous cell p53. To determine the relevance of oligomerization for transformation, miniproteins containing C-terminal portions of p53 were generated. These miniproteins, although carrying no point mutation, transformed at least as efficiently as full-length mutant p53. Transforming activity was coupled with the ability to oligomerize with wild-type p53, as well as with the ability to abrogate sequence-specific DNA binding by coexpressed wild-type p53. These findings suggest that p53-mediated transformation may operate through a dominant negative mechanism, involving the generation of DNA binding-incompetent oligomers.

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Metadata

Authors
Shaulian, E., Zauberman, A., Ginsberg, D., & Oren, M.
Venue
Molecular and Cellular Biology
Published
1992-12
Volume
12
Issue
12
Pages
5581-5592
ISSN
  • 0270-7306 (ISSN-L)
  • 1098-5549
OpenAlex
W2124380422
Cited by
342
References
5
FWCI
7.34
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Identification of a minimal transforming domain of p53: negative dominance through abrogation of sequence-specific DNA binding. https://app.cochat.ai/papers/10.1128/mcb.12.12.5581
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Shaulian, E., Zauberman, A., Ginsberg, D., & Oren, M. (1992). Identification of a minimal transforming domain of p53: negative dominance through abrogation of sequence-specific DNA binding. Molecular and Cellular Biology. https://doi.org/10.1128/mcb.12.12.5581

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