Cited by 455Cancer-related Molecular PathwaysCell death mechanisms and regulationHeat shock proteins research

Cyclin G is a transcriptional target of the p53 tumor suppressor protein.

Open access
Okamoto, K., Beach, D.·1994·The EMBO Journal

Abstract

Through a PCR-based differential screening method, cyclin G was identified as a novel transcriptional target of the p53 tumor suppressor gene product. In both a mouse p53 temperature-sensitive leukemic cell line and mouse embryonic fibroblasts (MEF) after gamma-irradiation, cyclin G mRNA was rapidly induced. MEF from a p53-deficient mouse expressed cyclin G at a level > 10-fold lower than that from a wild-type mouse. Using a DNA binding assay, a specific p53 binding site was identified upstream from the cyclin G gene, which functioned as a p53-dependent cis-acting element in a transient transfection assay. These results suggest that cyclin G might participate in a p53-mediated pathway to prevent tumorigenesis.

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Crossref · 10.1002/j.1460-2075.1994.tb06807.x

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  • MDM2 function is supported through cyclin G1, which activates MDM2 through dephosphorylation, and CCNG1 is a p53 target itself.

    “MDM2 function is supported through cyclin G1, which activates MDM2 through dephosphorylation218 and CCNG1 is a p53 target itself.219”

    From Census and evaluation of p53 target genes (2017) · cites this paper as [219]

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1 of the 40 references couldn’t be matched to a known paper.

Research works printed but not linked: 1

  1. Sambrook,J., Fritsch,E.F. and Maniatis,T. (1989) Molecular Cloning. A Laboratorv Manual. 2nd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.

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Authors
Okamoto, K., & Beach, D.
Affiliations
Howard Hughes Medical Institute (US)
Venue
The EMBO Journal
Published
1994-10-01
Volume
13
Issue
20
Pages
4816-4822
ISSN
  • 0261-4189 (ISSN-L)
  • 1460-2075
OpenAlex
W1823168351
Cited by
455
References
40
Citations by year
2026: 1 · 2025: 3 · 2024: 1 · 2023: 7 · 2022: 2 · 2021: 3 · 2020: 5 · 2019: 5 · 2018: 5 · 2017: 7 · 2016: 3 · 2015: 11 · 2014: 6 · 2013: 10 · 2012: 11
FWCI
15.16
Type
journal article
Language
en
Open access
Locations
  • The EMBO Journal (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
  • Institutional Repositories DataBase (IRDB) (submittedVersion)
Funders
  • Howard Hughes Medical Institute
  • National Institutes of Health
  • National Institute of General Medical Sciences (GM 396 20-06)
Topics
  • Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heat shock proteins research
Keywords
cyclin G, p53, transcription factor target genes, tumor suppressor, p53 binding sites, cis-regulatory elements, gamma irradiation, carcinogenesis, mouse embryonic fibroblasts, leukemia cell lines
MeSH terms
Amino Acid Sequence, Animals, Base Sequence, Cells, Cultured, Molecular Sequence Data, Protein Binding, Transcription Factors, Tumor Cells, Cultured, Transcriptional Activation, Tumor Suppressor Protein p53, Cyclins, Mice, Cyclin G, Cyclin G1

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