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沿特定DNA序列组装的核小体核心的原子力显微镜测量。

Atomic force microscope measurements of nucleosome cores assembled along defined DNA sequences.

作者信息

Allen M J, Dong X F, O'Neill T E, Yau P, Kowalczykowski S C, Gatewood J, Balhorn R, Bradbury E M

机构信息

Department of Biological Chemistry, School of Medicine, University of California, Davis 95616.

出版信息

Biochemistry. 1993 Aug 24;32(33):8390-6. doi: 10.1021/bi00084a002.

Abstract

We have found that the atomic force microscope (AFM) can be used to image the "beads-on-a-string" chromatin structure in a normal air environment following adsorption onto a cover glass substrate. Individual nucleosome cores and linker DNA could be resolved clearly along chromatin fibers that were reconstituted using histone octamers and a tandemly repeated 208-bp nucleosome positioning DNA sequence (208-18). AFM measurements showed that the compaction of the 3780-bp DNA by different loadings of histone octamers was consistent with 146 bp of DNA wrapped 1.75 turns about the histone octamer to form the 11-nm nucleosome core. Precise internucleosome core spacing measurements could be performed along the chromatin fiber axis. In other experiments, AFM images of chromatin reconstituted using closed circular DNA showed highly tangled beaded fibers, as expected. These images and measurements demonstrate that AFM can provide useful high-resolution structural information about chromatin that can be used to complement other more established techniques such as electron microscopy.

摘要

我们发现,原子力显微镜(AFM)可用于在吸附到盖玻片底物上后,在正常空气环境中对“串珠”染色质结构进行成像。沿着使用组蛋白八聚体和串联重复的208 bp核小体定位DNA序列(208 - 18)重构的染色质纤维,可以清晰分辨出单个核小体核心和连接DNA。原子力显微镜测量表明,不同加载量的组蛋白八聚体对3780 bp DNA的压缩与146 bp DNA围绕组蛋白八聚体缠绕1.75圈形成11 nm核小体核心的情况一致。可以沿着染色质纤维轴进行精确的核小体核心间距测量。在其他实验中,使用闭环DNA重构的染色质的原子力显微镜图像显示出高度缠结的珠状纤维,正如预期的那样。这些图像和测量结果表明,原子力显微镜可以提供有关染色质的有用高分辨率结构信息,可用于补充其他更成熟的技术,如电子显微镜。

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