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软X射线断层扫描揭示了体内神经发生过程中染色质的逐渐压缩和重组。

Soft X-Ray Tomography Reveals Gradual Chromatin Compaction and Reorganization during Neurogenesis In Vivo.

作者信息

Le Gros Mark A, Clowney E Josephine, Magklara Angeliki, Yen Angela, Markenscoff-Papadimitriou Eirene, Colquitt Bradley, Myllys Markko, Kellis Manolis, Lomvardas Stavros, Larabell Carolyn A

机构信息

Department of Anatomy, University of California San Francisco, San Francisco, CA 94158, USA; Physical Biosciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA; National Center for X-Ray Tomography, University of California San Francisco, San Francisco, CA 94158, USA; Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

Program in Biomedical Sciences, University of California San Francisco, San Francisco, CA 94158, USA.

出版信息

Cell Rep. 2016 Nov 15;17(8):2125-2136. doi: 10.1016/j.celrep.2016.10.060.

Abstract

The realization that nuclear distribution of DNA, RNA, and proteins differs between cell types and developmental stages suggests that nuclear organization serves regulatory functions. Understanding the logic of nuclear architecture and how it contributes to differentiation and cell fate commitment remains challenging. Here, we use soft X-ray tomography (SXT) to image chromatin organization, distribution, and biophysical properties during neurogenesis in vivo. Our analyses reveal that chromatin with similar biophysical properties forms an elaborate connected network throughout the entire nucleus. Although this interconnectivity is present in every developmental stage, differentiation proceeds with concomitant increase in chromatin compaction and re-distribution of condensed chromatin toward the nuclear core. HP1β, but not nucleosome spacing or phasing, regulates chromatin rearrangements because it governs both the compaction of chromatin and its interactions with the nuclear envelope. Our experiments introduce SXT as a powerful imaging technology for nuclear architecture.

摘要

DNA、RNA和蛋白质在细胞核中的分布因细胞类型和发育阶段而异,这表明细胞核组织具有调节功能。理解核结构的逻辑及其如何促进细胞分化和细胞命运决定仍然具有挑战性。在这里,我们使用软X射线断层扫描(SXT)对体内神经发生过程中的染色质组织、分布和生物物理特性进行成像。我们的分析表明,具有相似生物物理特性的染色质在整个细胞核中形成了一个复杂的连接网络。尽管这种相互连接性在每个发育阶段都存在,但随着染色质压缩的增加以及浓缩染色质向核核心的重新分布,细胞分化仍在进行。HP1β而非核小体间距或相位调节染色质重排,因为它既控制染色质的压缩,也控制其与核膜的相互作用。我们的实验将SXT引入为一种用于研究核结构的强大成像技术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09d0/5135017/11fabdf95da8/nihms827347f1.jpg

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