Abstract

The human POZ domain and Krüppel-like zinc finger (POK) family proteins play important roles in the regulation of apoptosis, cell proliferation, differentiation, development, oncogenesis, and tumor suppression. A novel POK family transcription factor, BTB/POZ and zinc finger domains factor on chromosome 1 (BOZF-1; also called ZBTB8A), contains a POZ domain and two C2H2-type Krüppel-like zinc fingers and is localized at nuclear speckles. Compared with paired normal tissues, BOZF1 expression is increased in cancer tissues of the prostate, breast, and cervix. BOZF1 repressed the transcription of p21WAF/CDKN1A by acting on the proximal promoter concentrated with Sp1-binding GC boxes. BOZF1 competed with Sp1 in binding to GC boxes 1-5/6 of the CDKN1A proximal promoter. In addition, BOZF1 interacted with p53 and decreased the acetylation of p53 by p300, which reduced the DNA binding activity of p53 at the far distal p53-binding element. BOZF1 blocked the two major molecular events that are important in both constitutive and inducible transcription activation of CDKN1A. BOZF1 is unique in that it bound to all the proximal GC boxes to repress transcription, and it inhibited p53 acetylation without affecting p53 stability. BOZF1 might be a novel proto-oncoprotein that stimulates cell proliferation.

Highlights

  • The POZ domain and Krüppel-like zinc finger (POK) proteins play roles in the regulation of the cell cycle, oncogenesis, and tumor suppression

  • Analysis of HEK293 cell growth showed that ectopic BOZF1 increased cell proliferation by 1.5-fold at day 6, and the knockdown of BOZF1 expression decreased cell proliferation by 1.6-fold (Fig. 1B). 3-(4,5Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assays showed that ectopic BOZF1 increased cell growth by 1.4fold at day 4 compared with the control, and the siRNAmediated knockdown of BOZF1 expression decreased cell growth by 1.8-fold

  • Some POK family proteins have been shown to be important in cell differentiation, development, and oncogenesis

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Summary

Background

The POK proteins play roles in the regulation of the cell cycle, oncogenesis, and tumor suppression. The human POZ domain and Krüppel-like zinc finger (POK) family proteins play important roles in the regulation of apoptosis, cell proliferation, differentiation, development, oncogenesis, and tumor suppression. In addition to inducible p53, Sp1 transcription factor activates CDKN1A transcription through binding at the six Sp1binding elements (GC boxes 1– 6) and plays an important role in the basal expression of p21 [30, 31]. The acetylation of p53 at Lys-373 and Lys-382 increases the stability, site-specific DNA binding, and p53 target gene expression (e.g. CDKN1A) [38, 39]. We found that BOZF1 increased cell proliferation by repressing CDKN1A expression through a molecular mechanism that involved the inhibition of p53 and Sp1 activity

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