Kim Daegeun, Setiaputra Dheva, Jung Taeyang, Chung Jaehee, Leitner Alexander, Yoon Jungmin, Aebersold Ruedi, Hebert Hans, Yip Calvin K, Song Ji-Joon
Department of Biological Sciences, KAIST Institute for the BioCentury, Cancer Metastasis Control Center, KAIST, 291 Daehakro Yuseong Daejeon, 34141, Korea.
Department of Biochemistry and Molecular Biology, The University of British Columbia, Vancouver, British Columbia, V6T 1Z3, Canada.
Sci Rep. 2016 May 25;6:26702. doi: 10.1038/srep26702.
Chromatin Assembly Complex 1 (CAF-1) is a major histone chaperone involved in deposition of histone H3 and H4 into nucleosome. CAF-1 is composed of three subunits; p150, p60 and p48 for human and Cac1, Cac2 and Cac3 for yeast. Despite of its central role in chromatin formation, structural features of the full CAF-1 in complex with histones and other chaperones have not been well characterized. Here, we dissect molecular architecture of yeast CAF-1 (yCAF-1) by cross-linking mass spectrometry (XL-MS) and negative stain single-particle electron microscopy (EM). Our work revealed that Cac1, the largest subunit of yCAF-1, might serve as a major histone binding platform linking Cac2 and Cac3. In addition, EM analysis showed that yCAF-1 adopts a bilobal shape and Cac1 connecting Cac2 and Cac3 to generate a platform for binding histones. This study provides the first structural glimpse of the full CAF-1 complex and a structural framework to understand histone chaperoning processes.
染色质组装复合体1(CAF-1)是一种主要的组蛋白伴侣,参与组蛋白H3和H4沉积到核小体中。CAF-1由三个亚基组成;人类的p150、p60和p48,以及酵母的Cac1、Cac2和Cac3。尽管CAF-1在染色质形成中起核心作用,但其与组蛋白和其他伴侣蛋白形成复合物时的完整结构特征尚未得到充分表征。在这里,我们通过交联质谱(XL-MS)和负染单颗粒电子显微镜(EM)剖析酵母CAF-1(yCAF-1)的分子结构。我们的工作表明,yCAF-1的最大亚基Cac1可能作为连接Cac2和Cac3的主要组蛋白结合平台。此外,EM分析表明yCAF-1呈双叶形状,Cac1连接Cac2和Cac3以形成一个结合组蛋白的平台。这项研究首次揭示了完整CAF-1复合物的结构,并提供了一个理解组蛋白伴侣过程的结构框架。