Abstract
p63 is a member of the p53 tumor suppressor family that is critical for epithelial differentiation and also has an important role in cancer progression. Currently, the molecular mechanisms governing regulation of p63 function remain largely unclear. This study identifies a unique E3 ubiquitin ligase for p63, SCF(betaTrCP1). SCF(betaTrCP1) is able to bind p63gamma isoforms, with a higher affinity for the TAp63gamma isoform. Strikingly, co-expression of TAp63gamma and betaTrCP1 leads to the stabilization of TAp63gamma. This stabilization of TAp63gamma leads to up-regulation of p21 at the mRNA and protein level by increased binding of TAp63gamma at the p21 promoter. The up-regulation of p21 causes a subsequent increase in G(1) phase cell cycle arrest. Last, SCF(betaTrCP1) is able to ubiquitylate TAp63gamma, and this ubiquitylation, as well as the increased activity of TAp63gamma, is ablated with the expression of a ubiquitin-deficient mutant of betaTrCP1 (DeltaFbetaTrCP1). Therefore, our study reveals that SCF(betaTrCP1) is an E3 ligase that activates p63 through ubiquitylation.
MeSH Terms
Animals
Blotting, Western
Cell Line
Cell Line, Tumor
DNA-Binding Proteins/genetics,metabolism
Humans
Immunoprecipitation
Models, Biological
Promoter Regions, Genetic/genetics
Protein Binding
Protein Isoforms/genetics,metabolism
RNA, Small Interfering/genetics
Reverse Transcriptase Polymerase Chain Reaction
Signal Transduction
Trans-Activators/genetics,metabolism
Transcription Factors
Transfection
Tumor Suppressor Proteins/genetics,metabolism
Ubiquitin-Protein Ligases/genetics,metabolism
Ubiquitination
Up-Regulation
Chemicals
DNA-Binding Proteins
Protein Isoforms
RNA, Small Interfering
TP63 protein, human
Trans-Activators
Transcription Factors
Tumor Suppressor Proteins
Ubiquitin-Protein Ligases
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Gallegos Jayme R
Department of Biochemistry and Molecular Biology, Oregon Health and Science University, Portland, Oregon 97239.
Litersky Joel
Department of Biochemistry and Molecular Biology, Oregon Health and Science University, Portland, Oregon 97239.
Lee Hunjoo
Department of Biochemistry and Molecular Biology, Oregon Health and Science University, Portland, Oregon 97239.
Sun Yi
Department of Radiation Oncology, University of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan 48109.
Nakayama Keiichi
Department of Molecular and Cellular Biology, Medical Institute of Bioregulation, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, Fukuoka 812-8582, Japan; CREST, Japan Science and Technology Agency, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan.
Nakayama Keiko
Department of Molecular and Cellular Biology, Medical Institute of Bioregulation, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, Fukuoka 812-8582, Japan; Department of Developmental Biology, Center for Translational and Advanced Animal Research, Graduate School of Medicine, Tohoku University, 2-1 Seiryo, Aoba-ku, Sendai 980-8575, Japan.
Lu Hua
Department of Biochemistry and Molecular Biology, Oregon Health and Science University, Portland, Oregon 97239; Department of Biochemistry and Molecular Biology, University of Indiana, Indianapolis, Indiana 46202. Electronic address: hualu@iupui.edu.