Journal Article

Structural insights into the π-π-π stacking mechanism and DNA-binding activity of the YEATS domain

Beloglazkina, Anastasia A., Shi, Xiaobing, Andrews, Forest H., Zhang, Jibo, Li, Yuanyuan, Kutateladze, Andrei G., Zhang, Yi, Liu, Wenshe R., Wang, Wesley W., Strahl, Brian D., Kutateladze, Tatiana G., Mi, Wenyi, Vann, Kendra R., Klein, Brianna J., Li, Haitao

2018

Overview

The YEATS domain has been identified as a reader of histone acylation and more recently emerged as a promising anti-cancer therapeutic target. Here, we detail the structural mechanisms for π-π-π stacking involving the YEATS domains of yeast Taf14 and human AF9 and acylated histone H3 peptides and explore DNA-binding activities of these domains. Taf14-YEATS selects for crotonyllysine, forming π stacking with both the crotonyl amide and the alkene moiety, whereas AF9-YEATS exhibits comparable affinities to saturated and unsaturated acyllysines, engaging them through π stacking with the acyl amide. Importantly, AF9-YEATS is capable of binding to DNA, whereas Taf14-YEATS is not. Using a structure-guided approach, we engineered a mutant of Taf14-YEATS that engages crotonyllysine through the aromatic-aliphatic-aromatic π stacking and shows high selectivity for the crotonyl H3K9 modification. Our findings shed light on the molecular principles underlying recognition of acyllysine marks and reveal a previously unidentified DNA-binding activity of AF9-YEATS. YEATS domains are histone acylation readers that recognize crotonyllysine and acetyllysine. Here the authors provide structural insights into how YEATS domains recognize acetyllysines and further show that the human AF9 YEATS domain also binds DNA.

• Publisher: Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
• Subject: 101/6 / 140/131 / 631/337/176 / 631/45/2783 / 631/535/1266 / 82/80 / Acetylation / Acylation / Aliphatic compounds / Binding / Cancer / Crystallography, X-Ray / Deoxyribonucleic acid / DNA / DNA - metabolism / DNA - ultrastructure / Domains / Histone Code / Histone H3 / Humanities and Social Sciences / Humans / Lysine - metabolism / multidisciplinary / Mutation / Nuclear Proteins - chemistry / Nuclear Proteins - metabolism / Nuclear Proteins - ultrastructure / Peptides / Protein Binding / Protein Domains / Saccharomyces cerevisiae Proteins - chemistry / Saccharomyces cerevisiae Proteins - genetics / Saccharomyces cerevisiae Proteins - metabolism / Saccharomyces cerevisiae Proteins - ultrastructure / Science / Science (multidisciplinary) / Selectivity / Stacking / Therapeutic applications / Transcription Factor TFIID - chemistry / Transcription Factor TFIID - genetics / Transcription Factor TFIID - metabolism / Transcription Factor TFIID - ultrastructure / Yeast