Structural mechanism of the bromodomain of the coactivator CBP in p53 transcriptional activation

S Mujtaba, Y He, L Zeng, S Yan, O Plotnikova… - Molecular cell, 2004 - cell.com
S Mujtaba, Y He, L Zeng, S Yan, O Plotnikova, R Sanchez, NJ Zeleznik-Le, Z Ronai
Molecular cell, 2004cell.com
Lysine acetylation of the tumor suppressor protein p53 in response to a wide variety of
cellular stress signals is required for its activation as a transcription factor that regulates cell
cycle arrest, senescence, or apoptosis. Here, we report that the conserved bromo-domain of
the transcriptional coactivator CBP (CREB binding protein) binds specifically to p53 at the C-
terminal acetylated lysine 382. This bromodomain/acetyl-lysine binding is responsible for
p53 acetylation-dependent coactivator recruitment after DNA damage, a step essential for …
Abstract
Lysine acetylation of the tumor suppressor protein p53 in response to a wide variety of cellular stress signals is required for its activation as a transcription factor that regulates cell cycle arrest, senescence, or apoptosis. Here, we report that the conserved bromo-domain of the transcriptional coactivator CBP (CREB binding protein) binds specifically to p53 at the C-terminal acetylated lysine 382. This bromodomain/acetyl-lysine binding is responsible for p53 acetylation-dependent coactivator recruitment after DNA damage, a step essential for p53-induced transcriptional activation of the cyclin-dependent kinase inhibitor p21 in G1 cell cycle arrest. We further present the three-dimensional nuclear magnetic resonance structure of the CBP bromodomain in complex with a lysine 382-acetylated p53 peptide. Using structural and biochemical analyses, we define the molecular determinants for the specificity of this molecular recognition.
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