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ZBTB2, a novel master regulator of the p53 pathway

Authors
 Bu-Nam Jeon  ;  Won-Il Choi  ;  Mi-Young Yu  ;  A-Rum Yoon  ;  Myung-Hwa Kim  ;  Chae-Ok Yun  ;  Man-Wook Hur 
Citation
 JOURNAL OF BIOLOGICAL CHEMISTRY, Vol.284(27) : 17935-17946, 2009 
Journal Title
 JOURNAL OF BIOLOGICAL CHEMISTRY 
ISSN
 0021-9258 
Issue Date
2009
MeSH
ADP-Ribosylation Factor 1/genetics ; ADP-Ribosylation Factor 1/metabolism ; Acetylation ; Animals ; Binding, Competitive/physiology ; Cell Division/physiology ; Cyclin-Dependent Kinase Inhibitor p21/genetics ; Cyclin-Dependent Kinase Inhibitor p21/metabolism ; DNA-Binding Proteins/chemistry ; DNA-Binding Proteins/genetics* ; DNA-Binding Proteins/metabolism* ; Drosophila ; HeLa Cells ; Histones/genetics ; Histones/metabolism ; Humans ; Kidney/cytology ; Mice ; Mice, Inbred Strains ; Promoter Regions, Genetic/physiology ; Protein Structure, Tertiary ; Proto-Oncogene Proteins c-mdm2/genetics ; Proto-Oncogene Proteins c-mdm2/metabolism ; RNA, Messenger/metabolism ; Repressor Proteins/chemistry ; Repressor Proteins/genetics* ; Repressor Proteins/metabolism* ; S Phase/physiology ; Sp1 Transcription Factor/metabolism ; Transcription Factors/chemistry ; Transcription Factors/genetics ; Transcription Factors/metabolism ; Transcription, Genetic/physiology ; Tumor Suppressor Protein p53/genetics* ; Tumor Suppressor Protein p53/metabolism* ; Two-Hybrid System Techniques
Abstract
We found that ZBTB2, a POK family transcription factor, is a potent repressor of the ARF-HDM2-p53-p21 pathway important in cell cycle regulation. ZBTB2 repressed transcription of the ARF, p53, and p21 genes, but activated the HDM2 gene. In particular, ZBTB2 repressed transcription of the p21 gene by acting on the two distal p53 binding elements and the proximal Sp1 binding GC-box 5/6 elements. ZBTB2 directly interacted with Sp1 via its POZ domain and zinc fingers, which was important in the repression of transcription activation by Sp1. ZBTB2 and Sp1 competed with each other in binding to the GC-box 5/6 elements and the two p53 binding elements. ZBTB2 directly interacted with p53 via its zinc fingers, inhibiting p53 binding and repressing transcription activation by p53. The POZ domain, required for transcription repression, interacted with corepressors such as BCoR, NCoR, and SMRT. The interactions deacetylated histones Ac-H3 and -H4 at the proximal promoter. Although ectopic ZBTB2 stimulated cell proliferation, knock-down of ZBTB2 expression decreased cell proliferation and DNA synthesis. Overall, our data suggest that ZBTB2 is a potential proto-oncogenic master control gene of the p53 pathway and, in particular, is a potent transcription repressor of the cell cycle arrest gene p21 by inhibiting p53 and Sp1.
Files in This Item:
T200901295.pdf Download
DOI
10.1074/jbc.M809559200
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
5. Research Institutes (연구소) > Institute for Cancer Research (암연구소) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Biochemistry and Molecular Biology (생화학-분자생물학교실) > 1. Journal Papers
Yonsei Authors
Kim, Myung Hwa(김명화)
Yu, Mi Young(유미영)
Yoon, A Rum(윤아름)
Yun, Chae Ok(윤채옥)
Jeon, Bu Nam(전부남)
Choi, Won Il(최원일)
Hur, Man Wook(허만욱) ORCID logo https://orcid.org/0000-0002-3416-1334
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/103889
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