1. Academic Validation
  2. DNA damage-inducible gene p33ING2 negatively regulates cell proliferation through acetylation of p53

DNA damage-inducible gene p33ING2 negatively regulates cell proliferation through acetylation of p53

  • Proc Natl Acad Sci U S A. 2001 Aug 14;98(17):9671-6. doi: 10.1073/pnas.161151798.
M Nagashima 1 M Shiseki K Miura K Hagiwara S P Linke R Pedeux X W Wang J Yokota K Riabowol C C Harris
Affiliations

Affiliation

  • 1 Laboratory of Human Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Abstract

The p33ING1 protein is a regulator of cell cycle, senescence, and Apoptosis. Three alternatively spliced transcripts of p33ING1 encode p47ING1a, p33ING1b, and p24ING1c. We cloned an additional ING family member, p33ING2/ING1L. Unlike p33ING1b, p33ING2 is induced by the DNA-damaging agents etoposide and neocarzinostatin. p33ING1b and p33ING2 negatively regulate cell growth and survival in a p53-dependent manner through induction of G(1)-phase cell-cycle arrest and Apoptosis. p33ING2 strongly enhances the transcriptional-transactivation activity of p53. Furthermore, p33ING2 expression increases the acetylation of p53 at Lys-382. Taken together, p33ING2 is a DNA damage-inducible gene that negatively regulates cell proliferation through activation of p53 by enhancing its acetylation.

Figures