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对活染色体中转录环的动态进行成像。

Imaging the dynamics of transcription loops in living chromosomes.

作者信息

Morgan Garry T

机构信息

School of Life Sciences, University of Nottingham, Queens Medical Centre, Nottingham, NG7 2UH, UK.

出版信息

Chromosoma. 2018 Sep;127(3):361-374. doi: 10.1007/s00412-018-0667-8. Epub 2018 Apr 3.

Abstract

When in the lampbrush configuration, chromosomes display thousands of visible DNA loops that are transcribed at exceptionally high rates by RNA polymerase II (pol II). These transcription loops provide unique opportunities to investigate not only the detailed architecture of pol II transcription sites but also the structural dynamics of chromosome looping, which is receiving fresh attention as the organizational principle underpinning the higher-order structure of all chromosome states. The approach described here allows for extended imaging of individual transcription loops and transcription units under conditions in which loop RNA synthesis continues. In intact nuclei from lampbrush-stage Xenopus oocytes isolated under mineral oil, highly specific targeting of fluorescent fusions of the RNA-binding protein CELF1 to nascent transcripts allowed functional transcription loops to be observed and their longevity assessed over time. Some individual loops remained extended and essentially static structures over time courses of up to an hour. However, others were less stable and shrank markedly over periods of 30-60 min in a manner that suggested that loop extension requires continued dense coverage with nascent transcripts. In stable loops and loop-derived structures, the molecular dynamics of the visible nascent RNP component were addressed using photokinetic approaches. The results suggested that CELF1 exchanges freely between the accumulated nascent RNP and the surrounding nucleoplasm, and that it exits RNP with similar kinetics to its entrance. Overall, it appears that on transcription loops, nascent transcripts contribute to a dynamic self-organizing structure that exemplifies a phase-separated nuclear compartment.

摘要

在灯刷染色体构型下,染色体呈现出数千个可见的DNA环,这些环由RNA聚合酶II(pol II)以极高的速率转录。这些转录环不仅为研究pol II转录位点的详细结构提供了独特的机会,也为研究染色体环化的结构动力学提供了机会,而染色体环化作为支撑所有染色体状态高阶结构的组织原则正受到新的关注。本文所述方法允许在环RNA合成持续的条件下对单个转录环和转录单元进行长时间成像。在矿物油下分离的灯刷期非洲爪蟾卵母细胞的完整细胞核中,将RNA结合蛋白CELF1的荧光融合物高度特异性地靶向新生转录本,使得功能性转录环得以观察,并能随时间评估其寿命。一些单个的环在长达一小时的时间进程中保持伸展且基本为静态结构。然而,其他一些环则不太稳定,在30 - 60分钟内明显收缩,这表明环的伸展需要新生转录本持续密集覆盖。在稳定的环和源自环的结构中,使用光动力学方法研究了可见新生核糖核蛋白(RNP)组分的分子动力学。结果表明,CELF1在积累的新生RNP和周围核质之间自由交换,并且它离开RNP的动力学与其进入时相似。总体而言,在转录环上,新生转录本似乎促成了一种动态的自组织结构,该结构例证了一个相分离的核区室。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77e2/6096578/026f8ef0fe8c/412_2018_667_Fig1_HTML.jpg

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