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Characterisation of human cyclin G1 and G2: DNA damage inducible genes

S Bates1, S Rowan, K H Vousden

  • 1ABL-Basic Research Program, NCI-FCRDC, Frederick, Maryland 21702-1201, USA.

Oncogene
|September 5, 1996
PubMed

Insights

Researchers identified human cyclin G1 and cyclin G2, finding both are induced by DNA damage. Cyclin G1

Area of Science:

  • Molecular Biology
  • Cell Cycle Regulation
  • Cancer Genetics

Background:

  • The p53 tumor suppressor protein regulates transcriptional targets.
  • Rodent cyclin G is a known p53-responsive gene.
  • The role of cyclin G in human p53-mediated functions requires elucidation.

Purpose of the Study:

  • To isolate and characterize human cyclin G1 and a related gene, cyclin G2.
  • To investigate the role of human G-cyclins in p53-mediated cellular responses.
  • To determine the p53 dependency of human cyclin G1 and G2 gene expression.

Main Methods:

  • Isolation of full-length human cyclin G1 and identification of cyclin G2.
  • Treatment of human cells with the DNA damaging agent actinomycin-D.
  • Analysis of cyclin G1 and G2 gene expression in response to DNA damage and p53 status.

Main Results:

  • Both human cyclin G1 and cyclin G2 were isolated.
  • Both G-cyclins are induced by actinomycin-D, a DNA damaging agent.
  • Cyclin G1 induction is p53-dependent, while cyclin G2 induction occurs independently of p53.

Conclusions:

  • Human cyclin G1 and G2 represent a distinct subgroup of cyclins.
  • Cyclin G1 acts as a p53-dependent gene, while cyclin G2 is induced independently of p53.
  • These findings suggest differential regulation and potential distinct roles for G-cyclins in cellular processes.

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