Modulation of p300/CBP acetylation of nucleosomes by bromodomain ligand I-CBP112

BE Zucconi, B Luef, W Xu, RA Henry, IM Nodelman… - Biochemistry, 2016 - ACS Publications
BE Zucconi, B Luef, W Xu, RA Henry, IM Nodelman, GD Bowman, AJ Andrews, PA Cole
Biochemistry, 2016ACS Publications
The histone acetyltransferase (HAT) enzymes p300 and CBP are closely related paralogs
that serve as transcriptional coactivators and have been found to be dysregulated in cancer
and other diseases. p300/CBP is a multidomain protein and possesses a highly conserved
bromodomain that has been shown to bind acetylated Lys residues in both proteins and
various small molecules, including I-CBP112 and CBP30. Here we show that the ligand I-
CBP112 can stimulate nucleosome acetylation up to 3-fold while CBP30 does not. Activation …
The histone acetyltransferase (HAT) enzymes p300 and CBP are closely related paralogs that serve as transcriptional coactivators and have been found to be dysregulated in cancer and other diseases. p300/CBP is a multidomain protein and possesses a highly conserved bromodomain that has been shown to bind acetylated Lys residues in both proteins and various small molecules, including I-CBP112 and CBP30. Here we show that the ligand I-CBP112 can stimulate nucleosome acetylation up to 3-fold while CBP30 does not. Activation of p300/CBP by I-CBP112 is not observed with the isolated histone H3 substrate but requires a nucleosome substrate. I-CBP112 does not impact nucleosome acetylation by the isolated p300 HAT domain, and the effects of I-CBP112 on p300/CBP can be neutralized by CBP30, suggesting that I-CBP112 likely allosterically activates p300/CBP through bromodomain interactions. Using mass spectrometry and Western blots, we have found that I-CBP112 particularly stimulates acetylation of Lys18 of histone H3 (H3K18) in nucleosomes, an established in vivo site of p300/CBP. In addition, we show that I-CBP112 enhances H3K18 acetylation in acute leukemia and prostate cancer cells in a concentration range commensurate with its antiproliferative effects. Our findings extend the known pharmacology of bromodomain ligands in the regulation of p300/CBP and suggest a novel approach to modulating histone acetylation in cancer.
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