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单细胞 DNA 表观遗传标记的成对邻近差异可视化。

Pairwise Proximity-Differentiated Visualization of Single-Cell DNA Epigenetic Marks.

机构信息

Institute of Analytical Chemistry and Instrument for Life Science, The Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Xi'an Jiaotong University, Xianning West Road, Xi'an, Shaanxi, 710049, China.

Institute of Molecular Medicine, Renji Hospital, School of Medicine and School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, 200127, China.

出版信息

Angew Chem Int Ed Engl. 2021 Feb 15;60(7):3428-3432. doi: 10.1002/anie.202011172. Epub 2020 Dec 21.

Abstract

Spatial positioning and proximity of relevant biomolecules such as DNA epigenetic marks are fundamental to a deeper understanding of life. However, it remains poorly explored and technically challenging. Here we report the pairwise proximity-differentiated visualization of single-cell 5-formylcytosine (5fC) and 5-hydroxymethylcytosine (5hmC). These two marks on chromatin in fixed cells are successively labeled and crosslinked with their DNA primer probes via click chemistry. Based on a pairwise proximity-differentiated mechanism, proximal 5fC/5hmC sites and residual 5fC or 5hmC sites are encoded with respective circularized barcodes. These barcodes are simultaneously amplified for multiplexed single-molecule imaging. We thus demonstrate the differentiated visualization of 5fC or 5hmC spatial positioning and their pairwise proximity in single cells. Such multi-level subcellular information may provide insights into regulation functions and mechanisms of chromatin modifications, and the spatial proximity can expose the potential crosstalk or interaction between their reader proteins.

摘要

空间定位和相关生物分子(如 DNA 表观遗传标记)的接近程度是深入了解生命的基础。然而,这方面的研究还很不深入,技术上也具有挑战性。在这里,我们报告了单细胞 5-甲酰胞嘧啶(5fC)和 5-羟甲基胞嘧啶(5hmC)的成对近邻差异化可视化。这两种在固定细胞染色质上的标记物通过点击化学与它们的 DNA 引物探针相继标记和交联。基于成对近邻差异化机制,近邻 5fC/5hmC 位点和残留的 5fC 或 5hmC 位点被各自的环状条形码编码。这些条形码被同时扩增,用于多重单细胞成像。因此,我们在单个细胞中演示了 5fC 或 5hmC 空间定位及其近邻的差异化可视化。这种多层次的亚细胞信息可能为研究染色质修饰的调控功能和机制提供新的思路,并且空间接近程度可以揭示它们的读取器蛋白之间潜在的串扰或相互作用。

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