Ramachandran Srinivas, Henikoff Steven
a Basic Sciences Division, Fred Hutchinson Cancer Research Center , Seattle , WA , USA.
b Howard Hughes Medical Institute , Seattle , WA , USA.
Nucleus. 2016;7(1):20-6. doi: 10.1080/19491034.2016.1149666. Epub 2016 Mar 2.
Precise positioning of nucleosomes around regulatory sites is achieved by the action of chromatin remodelers, which use the energy of ATP to slide, evict or change the composition of nucleosomes. Chromatin remodelers act to bind nucleosomes, disrupt histone-DNA interactions and translocate the DNA around the histone core to reposition nucleosomes. Hence, remodeling is expected to involve nucleosomal intermediates with a structural organization that is distinct from intact nucleosomes. We describe the identification of a partially unwrapped nucleosome structure using methods that map histone-DNA contacts genome-wide. This alternative nucleosome structure is likely formed as an intermediate or by-product during nucleosome remodeling by the RSC complex. Identification of the loss of histone-DNA contacts during chromatin remodeling by RSC in vivo has implications for the regulation of transcriptional initiation.
染色质重塑因子通过利用ATP的能量来滑动、驱逐或改变核小体的组成,从而实现核小体在调控位点周围的精确定位。染色质重塑因子作用于结合核小体,破坏组蛋白与DNA的相互作用,并使DNA围绕组蛋白核心移位以重新定位核小体。因此,重塑预计涉及具有与完整核小体不同结构组织的核小体中间体。我们描述了使用全基因组绘制组蛋白-DNA接触位点的方法鉴定一种部分解旋的核小体结构。这种替代性核小体结构可能是在RSC复合物进行核小体重塑过程中作为中间体或副产物形成的。在体内RSC进行染色质重塑过程中组蛋白-DNA接触位点丧失的鉴定对转录起始的调控具有重要意义。