Histone recognition and large-scale structural analysis of the human bromodomain family.

Article Details

Citation

Filippakopoulos P, Picaud S, Mangos M, Keates T, Lambert JP, Barsyte-Lovejoy D, Felletar I, Volkmer R, Muller S, Pawson T, Gingras AC, Arrowsmith CH, Knapp S

Histone recognition and large-scale structural analysis of the human bromodomain family.

Cell. 2012 Mar 30;149(1):214-31. doi: 10.1016/j.cell.2012.02.013.

PubMed ID
22464331 [ View in PubMed
]
Abstract

Bromodomains (BRDs) are protein interaction modules that specifically recognize epsilon-N-lysine acetylation motifs, a key event in the reading process of epigenetic marks. The 61 BRDs in the human genome cluster into eight families based on structure/sequence similarity. Here, we present 29 high-resolution crystal structures, covering all BRD families. Comprehensive crossfamily structural analysis identifies conserved and family-specific structural features that are necessary for specific acetylation-dependent substrate recognition. Screening of more than 30 representative BRDs against systematic histone-peptide arrays identifies new BRD substrates and reveals a strong influence of flanking posttranslational modifications, such as acetylation and phosphorylation, suggesting that BRDs recognize combinations of marks rather than singly acetylated sequences. We further uncovered a structural mechanism for the simultaneous binding and recognition of diverse diacetyl-containing peptides by BRD4. These data provide a foundation for structure-based drug design of specific inhibitors for this emerging target family.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Histone acetyltransferase KAT2BQ92831Details
CREB-binding proteinQ92793Details
Histone acetyltransferase KAT2AQ92830Details
Histone acetyltransferase p300Q09472Details