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一个隐秘的Tudor结构域将BRWD2/PHIP与COMPASS介导的组蛋白H3K4甲基化联系起来。

A cryptic Tudor domain links BRWD2/PHIP to COMPASS-mediated histone H3K4 methylation.

作者信息

Morgan Marc A J, Rickels Ryan A, Collings Clayton K, He Xiaolin, Cao Kaixiang, Herz Hans-Martin, Cozzolino Kira A, Abshiru Nebiyu A, Marshall Stacy A, Rendleman Emily J, Sze Christie C, Piunti Andrea, Kelleher Neil L, Savas Jeffrey N, Shilatifard Ali

机构信息

Department of Biochemistry and Molecular Genetics, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA.

Department of Cell and Molecular Biology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.

出版信息

Genes Dev. 2017 Oct 1;31(19):2003-2014. doi: 10.1101/gad.305201.117.

Abstract

Histone H3 Lys4 (H3K4) methylation is a chromatin feature enriched at gene -regulatory sequences such as promoters and enhancers. Here we identify an evolutionarily conserved factor, BRWD2/PHIP, which colocalizes with histone H3K4 methylation genome-wide in human cells, mouse embryonic stem cells, and Biochemical analysis of BRWD2 demonstrated an association with the Cullin-4-RING ubiquitin E3 ligase-4 (CRL4) complex, nucleosomes, and chromatin remodelers. BRWD2/PHIP binds directly to H3K4 methylation through a previously unidentified chromatin-binding module related to Royal Family Tudor domains, which we named the CryptoTudor domain. Using CRISPR-Cas9 genetic knockouts, we demonstrate that COMPASS H3K4 methyltransferase family members differentially regulate BRWD2/PHIP chromatin occupancy. Finally, we demonstrate that depletion of the single homolog dBRWD3 results in altered gene expression and aberrant patterns of histone H3 Lys27 acetylation at enhancers and promoters, suggesting a cross-talk between these chromatin modifications and transcription through the BRWD protein family.

摘要

组蛋白H3赖氨酸4(H3K4)甲基化是一种在基因调控序列(如启动子和增强子)中富集的染色质特征。在此,我们鉴定出一种进化上保守的因子BRWD2/PHIP,它在人类细胞、小鼠胚胎干细胞中与全基因组范围内的组蛋白H3K4甲基化共定位。对BRWD2的生化分析表明,它与Cullin-4-RING泛素E3连接酶4(CRL4)复合物、核小体和染色质重塑因子相关。BRWD2/PHIP通过一个与皇家家族 Tudor 结构域相关的先前未鉴定的染色质结合模块直接结合H3K4甲基化,我们将其命名为CryptoTudor结构域。使用CRISPR-Cas9基因敲除技术,我们证明COMPASS H3K4甲基转移酶家族成员对BRWD2/PHIP的染色质占据有不同的调节作用。最后,我们证明单个同源物dBRWD3的缺失会导致基因表达改变以及增强子和启动子处组蛋白H3赖氨酸27乙酰化模式异常,这表明这些染色质修饰与通过BRWD蛋白家族进行的转录之间存在相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4cab/5710144/a42831df1a72/2003f01.jpg

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