Department of Biochemistry and Molecular Biology, Center for Eukaryotic Gene Regulation, The Pennsylvania State University, University Park, PA 16802, USA.
Cell. 2012 Jun 22;149(7):1461-73. doi: 10.1016/j.cell.2012.04.036.
How chromatin remodelers cooperate to organize nucleosomes around the start and end of genes is not known. We determined the genome-wide binding of remodeler complexes SWI/SNF, RSC, ISW1a, ISW1b, ISW2, and INO80 to individual nucleosomes in Saccharomyces, and determined their functional contributions to nucleosome positioning through deletion analysis. We applied ultra-high-resolution ChIP-exo mapping to Isw2 to determine its subnucleosomal orientation and organization on a genomic scale. Remodelers interacted with selected nucleosome positions relative to the start and end of genes and produced net directionality in moving nucleosomes either away or toward nucleosome-free regions at the 5' and 3' ends of genes. Isw2 possessed a subnucleosomal organization in accord with biochemical and crystallographic-based models that place its linker binding region within promoters and abutted against Reb1-bound locations. Together, these findings reveal a coordinated position-specific approach taken by remodelers to organize genic nucleosomes into arrays.
染色质重塑复合物如何合作,将核小体组织在基因的起始和结束处尚不清楚。我们确定了重塑复合物 SWI/SNF、RSC、ISW1a、ISW1b、ISW2 和 INO80 在单个核小体上的全基因组结合,通过缺失分析确定了它们对核小体定位的功能贡献。我们应用超高分辨率 ChIP-exo 作图来确定 Isw2 的亚核小体取向和在基因组范围内的组织。重塑复合物与基因起始和结束处的选定核小体位置相互作用,并在基因 5' 和 3' 端的无核小体区域产生将核小体移出或移向的净方向性。Isw2 具有亚核小体组织,与基于生化和晶体学的模型一致,该模型将其连接子结合区域置于启动子内,并与 Reb1 结合的位置相邻。总之,这些发现揭示了重塑复合物以协调的位置特异性方法将基因核小体组织成阵列。