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New molecular bridge between RelA/p65 and NF-?B target genes via histone acetyltransferase TIP60 cofactor.


ABSTRACT: The nuclear factor-?B (NF-?B) family is involved in the expressions of numerous genes, in development, apoptosis, inflammatory responses, and oncogenesis. In this study we identified four NF-?B target genes that are modulated by TIP60. We also found that TIP60 interacts with the NF-?B RelA/p65 subunit and increases its transcriptional activity through protein-protein interaction. Although TIP60 binds with RelA/p65 using its histone acetyltransferase domain, TIP60 does not directly acetylate RelA/p65. However, TIP60 maintained acetylated Lys-310 RelA/p65 levels in the TNF-?-dependent NF-?B signaling pathway. In chromatin immunoprecipitation assay, TIP60 was primarily recruited to the IL-6, IL-8, C-IAP1, and XIAP promoters in TNF-? stimulation followed by acetylation of histones H3 and H4. Chromatin remodeling by TIP60 involved the sequential recruitment of acetyl-Lys-310 RelA/p65 to its target gene promoters. Furthermore, we showed that up-regulated TIP60 expression was correlated with acetyl-Lys-310 RelA/p65 expressions in hepatocarcinoma tissues. Taken together these results suggest that TIP60 is involved in the NF-?B pathway through protein interaction with RelA/p65 and that it modulates the transcriptional activity of RelA/p65 in NF-?B-dependent gene expression.

SUBMITTER: Kim JW 

PROVIDER: S-EPMC3293591 | biostudies-literature | 2012 Mar

REPOSITORIES: biostudies-literature

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New molecular bridge between RelA/p65 and NF-κB target genes via histone acetyltransferase TIP60 cofactor.

Kim Jung-Woong JW   Jang Sang-Min SM   Kim Chul-Hong CH   An Joo-Hee JH   Kang Eun-Jin EJ   Choi Kyung-Hee KH  

The Journal of biological chemistry 20120116 10


The nuclear factor-κB (NF-κB) family is involved in the expressions of numerous genes, in development, apoptosis, inflammatory responses, and oncogenesis. In this study we identified four NF-κB target genes that are modulated by TIP60. We also found that TIP60 interacts with the NF-κB RelA/p65 subunit and increases its transcriptional activity through protein-protein interaction. Although TIP60 binds with RelA/p65 using its histone acetyltransferase domain, TIP60 does not directly acetylate RelA  ...[more]

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