1. Academic Validation
  2. Human Kruppel-related 3 (HKR3) is a novel transcription activator of alternate reading frame (ARF) gene

Human Kruppel-related 3 (HKR3) is a novel transcription activator of alternate reading frame (ARF) gene

  • J Biol Chem. 2014 Feb 14;289(7):4018-31. doi: 10.1074/jbc.M113.526855.
Jae-Hyeon Yoon 1 Won-Il Choi Bu-Nam Jeon Dong-In Koh Min-Kyeong Kim Myung-Hwa Kim Jungho Kim Sujin Susanne Hur Kyung-Sup Kim Man-Wook Hur
Affiliations

Affiliation

  • 1 From the Department of Biochemistry and Molecular Biology, Brain Korea 21 PLUS Project for Medical Science, Severance Biomedical Science Institute, Yonsei University School of Medicine, 50 Yonsei-Ro, SeoDaeMun-Gu, Seoul 120-752, Korea.
Abstract

HKR3 (Human Krüppel-related 3) is a novel POK (POZ-domain Krüppel-like zinc-finger) family transcription factor. Recently, some of the POK (POZ-domain Krüppel-like zinc finger) family proteins have been shown to play roles in cell cycle arrest, Apoptosis, cell proliferation, and oncogenesis. We investigated whether HKR3, an inhibitor of cell proliferation and an uncharacterized POK family protein, could regulate the cell cycle by controlling expression of genes within the p53 pathway (ARF-MDM2-TP53-p21WAF/CDKN1A). HKR3 potently activated the transcription of the tumor suppressor gene ARF by acting on the proximal promoter region (bp, -149∼+53), which contains Sp1 and FBI-1 binding elements (FREs). HKR3 interacted with the co-activator p300 to activate ARF transcription, which increased the acetylation of histones H3 and H4 within the proximal promoter. Oligonucleotide pull-down assays and ChIP assays revealed that HKR3 interferes with the binding of the proto-oncogenic transcription repressor FBI-1 to proximal FREs, thus derepressing ARF transcription.

Keywords

ARF; Cell Cycle; Cell Proliferation; FBI-1; HKR3; POZ; Transcription; p300; p53.

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