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对内源性非重复基因组位点进行稳健的荧光标记和追踪。

Robust fluorescent labeling and tracking of endogenous non-repetitive genomic loci.

作者信息

Raterink Alex, Ghosh Rajarshi P, Yang Linfeng, Shi Quanming, Nguyen Minh Khue, Hilton Isaac B, Liphardt Jan T, Gustavsson Anna-Karin

出版信息

bioRxiv. 2025 Aug 27:2025.08.22.671818. doi: 10.1101/2025.08.22.671818.

Abstract

The spatial organization and dynamics of a genome are central to gene regulation. While a comprehensive understanding of chromatin organization in the human nucleus has been achieved using fixed-cell methods, measuring the dynamics of specific genomic regions over extended periods in individual living cells remains challenging. Here, we present a robust and fully genetically encoded system for fluorescent labeling and long-term tracking of any accessible non-repetitive genomic locus in live human cells using fluorogenic and replenishable nanobody array fusions of the dCas9, and compact polycistronic single guide (sg)RNAs. First, we characterize the selectivity and photostability of our probes, enabling genome-wide visualization of chromatin dynamics at locally repetitive elements. Next, through multiplexed expression of 8-10 sgRNAs from polycistronic cassettes, we demonstrate efficient and sustained labeling of non-repetitive loci, enabling high-fidelity tracking of gene-proximal regions at exceptional spatial and temporal resolution. Finally, by correlating chromatin mobility with transcriptional activity at multiple genes, we find that local chromatin dynamics at 20 Hz are gene-specific and not necessarily dependent on transcription. Our approach is versatile, minimally invasive, and scalable, enabling multiplexed imaging of regulatory element dynamics involved in gene control, with broad applicability across diverse biological systems and disease contexts.

摘要

基因组的空间组织和动态变化是基因调控的核心。虽然利用固定细胞方法已全面了解人类细胞核中的染色质组织,但在单个活细胞中长时间测量特定基因组区域的动态变化仍然具有挑战性。在此,我们展示了一种强大的、完全基于基因编码的系统,该系统利用dCas9的荧光生成和可补充纳米抗体阵列融合体以及紧凑的多顺反子单向导RNA(sgRNA),对活的人类细胞中任何可及的非重复基因组位点进行荧光标记和长期追踪。首先,我们表征了我们的探针的选择性和光稳定性,从而能够在全基因组范围内可视化局部重复元件处的染色质动态变化。接下来,通过从多顺反子盒中多路复用表达8 - 10个sgRNA,我们展示了对非重复位点的高效且持续的标记,从而能够以极高的空间和时间分辨率对基因近端区域进行高保真追踪。最后,通过将多个基因处的染色质迁移率与转录活性相关联,我们发现20赫兹的局部染色质动态变化是基因特异性的,不一定依赖于转录。我们的方法具有通用性、微创性且可扩展,能够对参与基因控制的调控元件动态变化进行多路复用成像,在各种生物系统和疾病背景中具有广泛的适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b58/12407769/1560d5f04146/nihpp-2025.08.22.671818v1-f0001.jpg

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