Graduate School of Human Development and Environment, Kobe University, Kobe, 657-8501, Japan.
Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka, 565-0871, Japan.
Chromosome Res. 2021 Mar;29(1):81-94. doi: 10.1007/s10577-021-09649-2. Epub 2021 Feb 22.
The chromosome compaction of chromatin fibers results in the formation of the nucleosome, which consists of a DNA unit coiled around a core of histone molecules associated with linker histone. The compaction of chromatin fibers has been a topic of controversy since the discovery of chromosomes in the 19th century. Although chromatin fibers were first identified using electron microscopy, the chromatin fibers on the surface of chromosome structures in plants remain unclear due to shrinking and breaking caused by prior chromosome isolation or preparation with alcohol and acid fixation, and critical point drying occurred into dehydration and denatured chromosomal proteins. This study aimed to develop a high-quality procedure for the isolation and preparation of plant chromosomes, maintaining the native chromosome structure, to elucidate the organization of chromatin fibers on the surface of plant chromosomes by electron microscopy. A simple technique to isolate intact barley (Hordeum vulgare) chromosomes with a high yield was developed, allowing chromosomes to be observed with a high-resolution scanning ion microscopy and helium ion microscopy (HIM) imaging technology, based on a scanning helium ion beam. HIM images from the surface chromatin fibers were analyzed to determine the size and alignment of the chromatin fibers. The unit size of the chromatin fibers was 11.6 ± 3.5 nm and was closely aligned to the chromatin network model. Our findings indicate that compacting the surface structure of barley via a chromatin network and observation via HIM are powerful tools for investigating the structure of chromatin.
染色质纤维的染色体紧缩导致核小体的形成,核小体由缠绕在与连接组蛋白相关的核心组蛋白分子周围的 DNA 单位组成。自 19 世纪发现染色体以来,染色质纤维的紧缩一直是一个有争议的话题。尽管最初使用电子显微镜鉴定染色质纤维,但由于先前的染色体分离或用酒精和酸固定剂进行的准备导致的收缩和断裂,以及临界点干燥导致脱水和变性的染色体蛋白,植物染色体结构表面的染色质纤维仍然不清楚。本研究旨在开发一种高质量的植物染色体分离和制备程序,保持天然染色体结构,通过电子显微镜阐明植物染色体表面染色质纤维的组织。开发了一种简单的技术来分离完整的大麦(Hordeum vulgare)染色体,产量高,允许使用高分辨率扫描离子显微镜和氦离子显微镜(HIM)成像技术观察染色体,基于扫描氦离子束。对来自表面染色质纤维的 HIM 图像进行了分析,以确定染色质纤维的大小和排列。染色质纤维的单元大小为 11.6 ± 3.5nm,与染色质网络模型紧密排列。我们的研究结果表明,通过染色质网络对大麦的表面结构进行紧缩,并通过 HIM 进行观察,是研究染色质结构的有力工具。