Skip NavigationSkip to Content

Association of Cdk2/Cyclin E and Nf-Kappa-B Complexes At G1/S Phase

  1. Author:
    Chen, E. Y.
    Li, C. C. H.
  2. Author Address

    Li CCH NCI FREDERICK CANC RES & DEV CTR SAIC FREDERICK INTRAMURAL RES SUPPORT PROGRAM FREDERICK, MD 21702 USA NCI FREDERICK CANC RES & DEV CTR SAIC FREDERICK INTRAMURAL RES SUPPORT PROGRAM FREDERICK, MD 21702 USA
    1. Year: 1998
  1. Journal: Biochemical and Biophysical Research Communications
    1. 249
    2. 3
    3. Pages: 728-734
  2. Type of Article: Article
  1. Abstract:

    NF-kappa B/Rel family plays a pivotal role in a wide variety of cellular functions including growth, development, apoptosis and stress responses. Recent studies indicated that NF-kappa B is also involved in the cell cycle regulation, and high expression of c-Rel results in a cell cycle arrest at the G1/S-phase transition (Bash, J., Zong, W.-X., and Gelinas, C. (1997) Mel. Cell. Biol. 17, 6526-6536). Here we report the detection of Cdk2, a critical kinase responsible for the G1/S-phase transition, in immune complexes precipitated by the NF-kappa B antisera. Cdk2 and NF-kappa B association was detected by co-precipitation in the nuclear lysates of the G1/S-phase cells, and was found in cultured cell lines and in T cells purified from human peripheral blood. Using an affinity column containing the C-terminal peptide of human c-Rel, we isolated cyclin E, the regulatory subunit of the Cdk2 complex, as a c-Rel-binding protein. These findings support and provide physical basis for the involvement of NF-kappa B in the G1/S-phase cell cycle control, and suggest an important role played by the C-terminal sequence of c-Rel. [References: 35]

    See More

External Sources

  1. No sources found.

Library Notes

  1. No notes added.
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel