Regular Article
The Central Region of Gadd45 Is Required for Its Interaction with p21/WAF1

https://doi.org/10.1006/excr.2000.4906Get rights and content

Abstract

Cell cycle arrest represents an important response to genotoxic stress and the tumor suppressor p53 has been described to act as a critical effector in this biological event. Upon stress, p53 becomes transcriptionally active and up-regulates the transcription of downstream effector genes, which contain p53 recognition sites in their regulatory regions. Among the genes activated are p21 and GADD45, each of which independently exhibits growth-suppressive activity. The Gadd45 protein has been described to form a complex with p21, and thus, work was undertaken to map the regions of Gadd45 involved in this interaction and to examine the roles of those two proteins in growth suppression. In this report, a Gadd45 overlapping peptide library and a series of Gadd45 deletion mutants were used to define the domains of Gadd45 involved in the association with p21. Results using both in vitro and in vivo methods have shown that the interaction of Gadd45 with p21 involves a central region of Gadd45. Interestingly, the p21-binding domain of Gadd45 also encodes the Cdc2-binding activity, indicating that the central region of Gadd45 may serve as an important “core,” through which Gadd45 protein is able to present cross-talk with other cell cycle regulators. In addition, GADD45 inhibition of Cdc2 kinase activity was compared with Myd118 and CR6, two other members of the GADD45 family. GADD45 was shown to generate the strongest inhibitory effect on Cdc2 activity. Finally, results from short-term survival assays further demonstrated that p21 and GADD45 act upon different cellular pathways to exert their growth-suppressive function.

References (43)

  • M.B Kastan et al.

    Cell

    (1992)
  • W.S el-Deiry et al.

    Cell

    (1993)
  • F Carrier et al.

    J. Biol. Chem.

    (1994)
  • M Takekawa et al.

    Cell

    (1998)
  • J Bartek et al.

    Curr. Opin. Cell Biol.

    (1996)
  • C Beadling et al.

    Semin. Immunol.

    (1993)
  • D.E Fisher

    Cell

    (1994)
  • L.H Hartwell et al.

    Science

    (1994)
  • S.J Kuerbitz et al.

    Proc. Natl. Acad. Sci. USA

    (1992)
  • Q Zhan et al.

    Cancer Res.

    (1994)
  • X Wu et al.

    Genes Dev.

    (1993)
  • T Miyashita et al.

    Cell

    (1995)
  • A.J Fornace et al.

    Proc. Natl. Acad. Sci. USA

    (1988)
  • M.A Papathanasiou et al.

    Mol. Cell. Biol.

    (1991)
  • Q Zhan et al.

    DNA Cell Biol.

    (1996)
  • Q Zhan et al.

    Mol. Cell. Biol.

    (1998)
  • Q Zhan et al.

    Mol. Cell. Biol.

    (1994)
  • M.L Smith et al.

    Science

    (1994)
  • Q Zhan et al.

    Oncogene

    (1999)
  • J.M Kearsey et al.

    Oncogene

    (1995)
  • J.W Harper et al.

    Cell

    (1993)
  • Cited by (57)

    • Correlation between the radiation responses of fibroblasts cultured from individual patients and the risk of late reaction after breast radiotherapy

      2016, Cancer Letters
      Citation Excerpt :

      However, expression of the endogenous cdk inhibitor p21/CDKN1A, which is a major transcriptional target of p53 and part of the stress-induced G1/S cell-cycle checkpoint, was not associated with late reaction. Instead, we speculate that another p53 transcriptional target GADD45, which plays important roles in genomic stability and differentiation [55–57], might be involved, in which case it might target the G2/M rather than the G1/S checkpoint [58]. In conclusion, we have found a small but significant increase in the number of residual DSBs and a consistently higher fraction of p53-positive cells without irradiation, as well as 2 h and 6 d after in vitro irradiation of fibroblasts from RT-sensitive versus RT-resistant patients.

    • Inhibitory effect of isoamericanol A from Jatropha curcas seeds on the growth of MCF-7 human breast cancer cell line by G2/M cell cycle arrest

      2016, Heliyon
      Citation Excerpt :

      In human breast cancer cell lines, such as MDA-MB-231 or MCF-7, BTG2 mRNA expression is generally undetectably low [24], and it is one of the tumor suppressor genes that inactivates the cyclin B1/CDK1 complex [25, 26]. GADD45A and p21 bind to CDK1, resulting in dissociation of the cyclin B/CDK1 complex and eventually induction of cell cycle arrest at G2/M [18, 27, 28]. As clearly shown in our data of cell cycle analysis (Fig. 3), western blot analysis (Fig. 5) and real-time PCR (Fig. 6), IAA treatment initiated G2/M arrest on MCF-7 by the increased expression of BTG2, p21, and GADD45A.

    • Gadd45 proteins: Relevance to aging, longevity and age-related pathologies

      2012, Ageing Research Reviews
      Citation Excerpt :

      This important regulator of cell cycle is deeply involved in cellular senescence, cancer, atherosclerosis, and diabetes (Chang et al., 2000). Its interaction with Gadd45 was shown to inhibit cell growth and as such, could be part of p21-mediated tumor suppressor activity (Zhao et al., 2000). Apart from direct protein–protein interactions, there are numerous regulatory links between Gadd45 and well known players in ARDs, such as p53, p38, JNK, FOXO, SIRT1, HDAC, and others (see previous sections and Fig. 3).

    • GADD45A: With or without you

      2024, Medicinal Research Reviews
    View all citing articles on Scopus
    1

    To whom correspondence and reprint requests should be addressed. Fax: (412)-624-0295. E-mail: [email protected].

    View full text