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人类G1期和中期染色质的纳米级原位分析。

Nanoscale analysis of human G1 and metaphase chromatin in situ.

作者信息

Chen Jon Ken, Liu Tingsheng, Cai Shujun, Ruan Weimei, Ng Cai Tong, Shi Jian, Surana Uttam, Gan Lu

机构信息

Department of Biological Sciences and Centre for BioImaging Sciences, National University of Singapore, Singapore, 117543, Singapore.

Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA, 22903, USA.

出版信息

EMBO J. 2025 May;44(9):2658-2694. doi: 10.1038/s44318-025-00407-2. Epub 2025 Mar 17.

Abstract

The structure of chromatin at the nucleosome level inside cells is still incompletely understood. Here we present in situ electron cryotomography analyses of chromatin in both G1 and metaphase RPE-1 cells. G1 nucleosomes are concentrated in globular chromatin domains, and metaphase nucleosomes are concentrated in the chromatids. Classification analysis reveals that canonical mononucleosomes, and in some conditions ordered stacked dinucleosomes and mononucleosomes with a disordered gyre-proximal density, are abundant in both cell-cycle states. We do not detect class averages that have more than two stacked nucleosomes or side-by-side dinucleosomes, suggesting that groups of more than two nucleosomes are heterogeneous. Large multi-megadalton structures are abundant in G1 nucleoplasm, but not found in G1 chromatin domains and metaphase chromatin. The macromolecular phenotypes studied here represent a starting point for the comparative analysis of compaction in normal vs. unhealthy human cells, in other cell-cycle states, other organisms, and in vitro chromatin assemblies.

摘要

细胞内核小体水平的染色质结构仍未完全明晰。在此,我们展示了对处于G1期和中期的RPE-1细胞中染色质的原位电子冷冻断层扫描分析。G1期核小体集中于球状染色质结构域,中期核小体集中于染色单体。分类分析表明,在两种细胞周期状态下,典型单核小体以及在某些条件下有序堆叠的双核小体和具有无序螺旋近端密度的单核小体都很丰富。我们未检测到具有超过两个堆叠核小体或并排双核小体的类平均值,这表明超过两个核小体的群体是异质性的。大的多兆道尔顿结构在G1期核质中丰富,但在G1期染色质结构域和中期染色质中未发现。此处研究的大分子表型代表了对正常与不健康人类细胞、其他细胞周期状态、其他生物体以及体外染色质组装体中的压缩进行比较分析的起点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88d2/12048539/dfe907986b43/44318_2025_407_Fig1_HTML.jpg

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