Abstract

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/p65. However, TIP60 maintained acetylated Lys-310 RelA/p65 levels in the TNF-α-dependent NF-κB signaling pathway. In chromatin immunoprecipitation assay, TIP60 was primarily recruited to the IL-6, IL-8, C-IAP1, and XIAP promoters in TNF-α 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-κB pathway through protein interaction with RelA/p65 and that it modulates the transcriptional activity of RelA/p65 in NF-κB-dependent gene expression.

Highlights

  • TIP60 is involved in transcriptional regulation acting as a coactivator or corepressor

  • To confirm TIP60-mediated transcriptional enhancement on nuclear factor-␬B (NF-␬B) target genes, HEK 293 cells were transfected with the FLAG-TIP60 plasmid, and the mRNA expression was analyzed by semiquantitative RT-polymerase chain reaction (PCR)

  • Growing evidence suggests that TIP60 plays an important role in the transcriptional regulation of transcription factors acting as coactivator or corepressor, TIP60-mediated gene expression regulation is not well determined

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Summary

Background

TIP60 is involved in transcriptional regulation acting as a coactivator or corepressor. Chromatin remodeling by TIP60 involved the sequential recruitment of acetyl-Lys-310 RelA/p65 to its target gene promoters. 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. Transcriptional activation of NF-␬B involves the association of NF-␬B with various cofactors including histone acetyltransferase (HAT) p300/CBP and the nuclear receptor coactivators SRC3/Rac and SRC1/N-CoA1 (18 –21). It is generally accepted that TFs primarily bind to specific promoters and trigger a recruitment cascade of coactivator complexes, interestingly, we found that TIP60 appeared and bound earlier to the NF-␬B target promoters than RelA/65, and it simultaneously promoted the acetylation of histones. Site-specific early association of TIP60 could serve as the platform for transcription factor RelA/p65 binding sites to promote NF-␬B-mediated gene expression

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