Buning Ruth, Kropff Wietske, Martens Kirsten, van Noort John
Huygens-Kamerlingh Onnes Laboratory, Leiden University, Niels Bohrweg 2, 2333 CA Leiden, The Netherlands.
J Phys Condens Matter. 2015 Feb 18;27(6):064103. doi: 10.1088/0953-8984/27/6/064103. Epub 2015 Jan 7.
Chromatin, the structure in which DNA is compacted in eukaryotic cells, plays a key role in regulating DNA accessibility. FRET experiments on single nucleosomes, the basic units in chromatin, have revealed a dynamic nucleosome where spontaneous DNA unwrapping from the ends provides access to the nucleosomal DNA. Here we investigated how this DNA breathing is affected by extension of the linker DNA and by the presence of a neighboring nucleosome. We found that both electrostatic interactions between the entering and exiting linker DNA and nucleosome-nucleosome interactions increase unwrapping. Interactions between neighboring nucleosomes are more likely in dinucleosomes spaced by 55 bp of linker DNA than in dinucleosomes spaced by 50 bp of linker DNA. Such increased unwrapping may not only increase the accessibility of nucleosomal DNA in chromatin fibers, it may also be key to folding of nucleosomes into higher order structures.
染色质是真核细胞中DNA压缩形成的结构,在调节DNA可及性方面发挥关键作用。对染色质基本单位单核小体进行的荧光共振能量转移实验揭示了一种动态核小体,其中DNA从末端自发解旋可使核小体DNA得以暴露。在此,我们研究了连接DNA的延长以及相邻核小体的存在如何影响这种DNA呼吸作用。我们发现,进入和离开的连接DNA之间的静电相互作用以及核小体-核小体相互作用都会增加解旋。与由50 bp连接DNA隔开的双核小体相比,由55 bp连接DNA隔开的双核小体中相邻核小体之间的相互作用更有可能发生。这种增加的解旋不仅可能增加染色质纤维中核小体DNA的可及性,还可能是核小体折叠成更高阶结构的关键。