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SiCLAT:活细胞中染色质环和活性转录的同步成像

SiCLAT: simultaneous imaging of chromatin loops and active transcription in living cells.

作者信息

Wan Xin, Kong Jie, Hu Xiaodi, Liu Lulu, Yang Yuanping, Li Hu, Liu Gaoao, Niu Xingchen, Chen Fengling, Zhang Dan, Zhu Dahai, Zhang Yong

机构信息

State Key Laboratory for Complex, Severe, and Rare Diseases, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and School of Basic Medicine, Peking Union Medical College, Beijing, China.

Center for Biomedical Technology of National Infrastructures for Translational Medicine, State Key Laboratory of Complex, Severe, and Rare Diseases in Peking Union Medical College Hospital, Beijing, China.

出版信息

Genome Biol. 2025 Jan 2;26(1):1. doi: 10.1186/s13059-024-03463-9.

Abstract

We present SiCLAT, which introduces a dCas9-dCas13d cassette into the mouse genome. This model enables the stable expression of both dCas9 and dCas13 proteins in diverse cell populations, facilitating concurrent labeling of DNA and RNA across various cell types. Using SiCLAT, we accurately labeled chromatin loop anchor interactions and associated gene transcription during myogenic differentiation. This imaging system offers a novel means of directly observing cis-element interactions and the corresponding gene transcription in living primary cells, thus providing real-time imaging for comprehensive mechanistic investigations of dynamic enhancer-promoter or enhancer-enhancer interactions in regulating transcription activation within living cells.

摘要

我们展示了SiCLAT,它将dCas9-dCas13d盒式结构引入小鼠基因组。该模型能够在不同细胞群体中稳定表达dCas9和dCas13蛋白,便于在各种细胞类型中同时标记DNA和RNA。利用SiCLAT,我们在成肌分化过程中准确标记了染色质环锚定相互作用和相关基因转录。该成像系统提供了一种直接观察活原代细胞中顺式元件相互作用和相应基因转录的新方法,从而为全面深入研究活细胞中动态增强子-启动子或增强子-增强子相互作用调控转录激活的机制提供实时成像。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b25/11694377/3b5f4443f9d4/13059_2024_3463_Fig1_HTML.jpg

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