Cancer Research Translational Cancer Medicine 2008: Cancer Clinical Trials and Personalized Medicine  Joint Metastasis Research Society-AACR Conference on Metastasis
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[Cancer Research 63, 2373-2378, May 15, 2003]
© 2003 American Association for Cancer Research


Advances in Brief

p29ING4 and p28ING5 Bind to p53 and p300, and Enhance p53 Activity

Masayuki Shiseki, Makoto Nagashima, Remy M. Pedeux, Mariko Kitahama-Shiseki, Koh Miura, Shu Okamura, Hitoshi Onogi, Yuichiro Higashimoto, Ettore Appella, Jun Yokota and Curtis C. Harris1

Laboratories of Human Carcinogenesis [M. S., M. N., R. M. P., M. K-S., K. M., S. O., H. O., C. C. H.] and Cell Biology [Y. H., E. A.], Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland 20892-4255, and Biology Division, National Cancer Center Research Institute, Tokyo 104, Japan [J. Y.]

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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