McGinty Robert K, Tan Song
Center for Eukaryotic Gene Regulation, Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA 16802, USA.
Center for Eukaryotic Gene Regulation, Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA 16802, USA.
Curr Opin Struct Biol. 2016 Apr;37:54-61. doi: 10.1016/j.sbi.2015.11.014. Epub 2016 Jan 5.
Dynamic expression of the genome requires coordinated binding of chromatin factors and enzymes that carry out genome-templated processes. Until recently, the molecular mechanisms governing how these factors and enzymes recognize and act on the fundamental unit of chromatin, the nucleosome core particle, have remained a mystery. A small, yet growing set of structures of the nucleosome in complex with chromatin factors and enzymes highlights the importance of multivalency in defining nucleosome binding and specificity. Many such interactions include an arginine anchor motif, which targets a unique acidic patch on the nucleosome surface. These emerging paradigms for chromatin recognition will be discussed, focusing on several recent structural breakthroughs.
基因组的动态表达需要染色质因子和执行基因组模板化过程的酶的协同结合。直到最近,控制这些因子和酶如何识别染色质基本单位核小体核心颗粒并对其起作用的分子机制仍是个谜。与染色质因子和酶形成复合物的核小体的一小部分且数量不断增加的结构,突出了多价性在定义核小体结合和特异性方面的重要性。许多这样的相互作用包括一个精氨酸锚定基序,它靶向核小体表面一个独特的酸性区域。将讨论这些新兴的染色质识别范式,重点关注最近的几个结构突破。