1. Academic Validation
  2. p29ING4 and p28ING5 bind to p53 and p300, and enhance p53 activity

p29ING4 and p28ING5 bind to p53 and p300, and enhance p53 activity

  • Cancer Res. 2003 May 15;63(10):2373-8.
Masayuki Shiseki 1 Makoto Nagashima Remy M Pedeux Mariko Kitahama-Shiseki Koh Miura Shu Okamura Hitoshi Onogi Yuichiro Higashimoto Ettore Appella Jun Yokota Curtis C Harris
Affiliations

Affiliation

  • 1 Laboratories of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland 20892-4255, USA.
PMID: 12750254
Abstract

We identified and characterized two new ING family genes, p29ING4 and p28ING5,coding for two proteins of 249 and 240 Amino acids, respectively. Both p29ING4 and p28ING5 proteins have a plant homeodomain finger motif also found in other ING proteins, and which is common in proteins involved in chromatin remodeling. p29ING4 or p28ING5 overexpression resulted in a diminished colony-forming efficiency, a decreased cell population in S phase, and the induction of Apoptosis in a p53-dependent manner. Both p29ING4 and p28ING5 activate the p21/waf1 promoter, and induce p21/WAF1 expression. p29ING4 and p28ING5 enhance p53 acetylation at Lys-382 residues, and physically interact with p300, a member of histone acetyl transferase complexes, and p53 in vivo. These results indicate that p29ING4 and p28ING5 may be significant modulators of p53 function.

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