Li Gu, Levitus Marcia, Bustamante Carlos, Widom Jonathan
Department of Biochemistry, Molecular Biology, and Cell Biology, Northwestern University, Evanston, Illinois 60208-3500, USA.
Nat Struct Mol Biol. 2005 Jan;12(1):46-53. doi: 10.1038/nsmb869. Epub 2004 Dec 5.
DNA wrapped in nucleosomes is sterically occluded, creating obstacles for proteins that must bind it. How proteins gain access to DNA buried inside nucleosomes is not known. Here we report measurements of the rates of spontaneous nucleosome conformational changes in which a stretch of DNA transiently unwraps off the histone surface, starting from one end of the nucleosome, and then rewraps. The rates are rapid. Nucleosomal DNA remains fully wrapped for only approximately 250 ms before spontaneously unwrapping; unwrapped DNA rewraps within approximately 10-50 ms. Spontaneous unwrapping of nucleosomal DNA allows any protein rapid access even to buried stretches of the DNA. Our results explain how remodeling factors can be recruited to particular nucleosomes on a biologically relevant timescale, and they imply that the major impediment to entry of RNA polymerase into a nucleosome is rewrapping of nucleosomal DNA, not unwrapping.
包裹在核小体中的DNA在空间上被遮挡,这为必须与之结合的蛋白质制造了障碍。蛋白质如何接触到埋在核小体内部的DNA尚不清楚。在这里,我们报告了对核小体构象自发变化速率的测量结果,其中一段DNA从核小体的一端开始短暂地从组蛋白表面解开,然后重新包裹。这些速率很快。核小体DNA在自发解开之前仅完全包裹约250毫秒;解开的DNA在约10 - 50毫秒内重新包裹。核小体DNA的自发解开使任何蛋白质都能快速接触到即使是被掩埋的DNA片段。我们的结果解释了重塑因子如何在生物学相关的时间尺度上被招募到特定的核小体上,并且暗示RNA聚合酶进入核小体的主要障碍是核小体DNA的重新包裹,而不是解开。