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Cited by 341

The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

JNK targets p53 ubiquitination and degradation in nonstressed cells

Open access
Fuchs, Serge Y., Adler, Victor, Buschmann, Thomas, Yin, Zhimin, Wu, Xiangwei, Jones, Stephen N., Ronai, Ze’ev·1998·Genes & Development

Abstract

In this study we elucidated the role of nonactive JNK in regulating p53 stability. The amount of p53–JNK complex was inversely correlated with p53 level. A peptide corresponding to the JNK binding site on p53 efficiently blocked ubiquitination of p53. Similarly, p53 lacking the JNK binding site exhibits a longer half-life than p53 wt. Outcompeting JNK association with p53 increased the level of p53, whereas overexpression of a phosphorylation mutant form of JNK inhibited p53 accumulation. JNK–p53 and Mdm2–p53 complexes were preferentially found in G 0/G 1 and S/G 2 M phases of the cell cycle, respectively. Altogether, these data indicate that JNK is an Mdm2-independent regulator of p53 stability in nonstressed cells.

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Metadata

Authors
Fuchs, S. Y., Adler, V., Buschmann, T., Yin, Z., Wu, X., Jones, S. N., & Ronai, Z.
Venue
Genes & Development
Published
1998-09-01
Volume
12
Issue
17
Pages
2658-2663
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W2113070607
Cited by
341
References
6
Type
posted content
Language
en
Open access
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CoChat. (2026). Citation check: JNK targets p53 ubiquitination and degradation in nonstressed cells. https://app.cochat.ai/papers/10.1101/gad.12.17.2658
The paper
Fuchs, S. Y., Adler, V., Buschmann, T., Yin, Z., Wu, X., Jones, S. N., & Ronai, Z. (1998). JNK targets p53 ubiquitination and degradation in nonstressed cells. Genes & Development. https://doi.org/10.1101/gad.12.17.2658

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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