4.6 Article

ZBTB2, a Novel Master Regulator of the p53 Pathway

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 284, Issue 27, Pages 17935-17946

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M809559200

Keywords

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Funding

  1. National Research Laboratory Research [ROA-2003-000-10318-0, M10416130002-04N1613-00210, R15-2004-024-02001-0]
  2. Medical Research Center
  3. Korean Science and Engineering Foundation of the Korean Ministry of Science and Technology [R13-2002-054-05002-0]
  4. Korean Ministry for Health, Welfare and Family Affairs [00001561]
  5. National Research Foundation of Korea [R13-2002-054-05002-0] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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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, knockdown 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.

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