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PMID: 7478510 Published · ppublish English Comparative Study Journal Article

Direct interaction of Gadd45 with PCNA and evidence for competitive interaction of Gadd45 and p21Waf1/Cip1 with PCNA.

Oncogene ·Vol. 11 ·No. 10 ·1995-11-16 ·Pages 1931-7

Chen IT, Smith ML, O'Connor PM, Fornace AJ

Abstract

We have previously shown (Smith et al., 1994) that antibodies raised against the growth arrest and DNA damage inducible protein Gadd45 co-precipitate proliferating cell nuclear antigen (PCNA), a protein involved in DNA replication and repair. Here we demonstrate that Gadd45 can directly bind to PCNA using a Far-western blotting approach. In this assay, a Gadd45 bacterial expression vector was modified to allow synthesis of purified 32P-labeled Gadd45 fusion protein. This protein was used to detect filter bound PCNA protein, while filter bound Gadd45 protein could also be detected by free PCNA molecules. Using recombinant proteins in conjunction with immunoprecipitation and immunoblotting, we show that Gadd45 competes with p21 for binding to PCNA and conversely, p21 blocks the ability of Gadd45 to bind PCNA. In addition, p21 appears to disrupt PCNA trimers whereas Gadd45 has a lesser effect. PCNA trimer disruption was also observed in UV-irradiated cells but not in repair-defective xeroderma pigmentosum group A (XP-A) cells.

MeSH Terms
Base Sequence Binding, Competitive Blotting, Western/methods Colonic Neoplasms/metabolism Cyclin-Dependent Kinase Inhibitor p21 Cyclins/metabolism,pharmacology DNA Damage Drug Interactions Fibroblasts/metabolism,radiation effects Humans Intracellular Signaling Peptides and Proteins Lung Neoplasms/metabolism Macromolecular Substances Molecular Sequence Data Proliferating Cell Nuclear Antigen/drug effects,metabolism Proteins/metabolism,pharmacology Recombinant Proteins/metabolism Tumor Cells, Cultured/radiation effects Ultraviolet Rays
Chemicals
CDKN1A protein, human Cyclin-Dependent Kinase Inhibitor p21 Cyclins GADD45 protein Intracellular Signaling Peptides and Proteins Macromolecular Substances Proliferating Cell Nuclear Antigen Proteins Recombinant Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Chen I T
Laboratory of Molecular Pharmacology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Smith M L
O'Connor P M
Fornace A J
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1995-11-16
Pages
1931-7
Language
English
Region
England
NLM ID
8711562
Subset
IM
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