Tremblay Véronique, Zhang Pamela, Chaturvedi Chandra-Prakash, Thornton Janet, Brunzelle Joseph S, Skiniotis Georgios, Shilatifard Ali, Brand Marjorie, Couture Jean-François
Ottawa Institute of Systems Biology, Department of Biochemistry, Microbiology and Immunology, University of Ottawa, 451 Smyth Road, Ottawa, ON K1H 8M5, Canada.
The Sprott Center for Stem Cell Research, Regenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, ON K1H 8L6, Canada; Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON K1H 8L6, Canada.
Structure. 2014 Dec 2;22(12):1821-1830. doi: 10.1016/j.str.2014.10.002. Epub 2014 Nov 20.
DPY-30 is a subunit of mammalian COMPASS-like complexes (complex of proteins associated with Set1) and regulates global histone H3 Lys-4 trimethylation. Here we report structural evidence showing that the incorporation of DPY-30 into COMPASS-like complexes is mediated by several hydrophobic interactions between an amphipathic α helix located on the C terminus of COMPASS subunit ASH2L and the inner surface of the DPY-30 dimerization/docking (D/D) module. Mutations impairing the interaction between ASH2L and DPY-30 result in a loss of histone H3K4me3 at the β locus control region and cause a delay in erythroid cell terminal differentiation. Using overlay assays, we defined a consensus sequence for DPY-30 binding proteins and found that DPY-30 interacts with BAP18, a subunit of the nucleosome remodeling factor complex. Overall, our results indicate that the ASH2L/DPY-30 complex is important for cell differentiation and provide insights into the ability of DPY-30 to associate with functionally divergent multisubunit complexes.
DPY-30是哺乳动物类COMPASS复合物(与Set1相关的蛋白质复合物)的一个亚基,可调节整体组蛋白H3赖氨酸-4三甲基化。在此我们报告结构证据,表明DPY-30纳入类COMPASS复合物是由COMPASS亚基ASH2L C末端的一个两亲性α螺旋与DPY-30二聚化/对接(D/D)模块的内表面之间的几种疏水相互作用介导的。破坏ASH2L与DPY-30之间相互作用的突变导致β基因座控制区组蛋白H3K4me3缺失,并导致红系细胞终末分化延迟。通过覆盖分析,我们确定了DPY-30结合蛋白的共有序列,并发现DPY-30与核小体重塑因子复合物的一个亚基BAP18相互作用。总体而言,我们的结果表明ASH2L/DPY-30复合物对细胞分化很重要,并为DPY-30与功能不同的多亚基复合物结合的能力提供了见解。