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Cut-C:在束缚核酸酶下的切割用于构象捕获。

Cut-C: cleavage under tethered nuclease for conformational capture.

机构信息

Department of Stem Cell Therapy Science, Graduate School of Medicine, Osaka University, Suita, Osaka, 5650871, Japan.

StemRIM Co., Ltd., Ibaraki, Osaka, 5670085, Japan.

出版信息

BMC Genomics. 2019 Jul 29;20(1):614. doi: 10.1186/s12864-019-5989-2.

Abstract

BACKGROUND

Deciphering the 3D structure of the genome is essential for elucidating the regulatory mechanisms of gene expression in detail. Existing methods, such as chromosome conformation capture (3C) and Hi-C have enabled the identification of novel aspects of chromatin structure. Further identification of protein-centric chromatin conformation is enabled by coupling the Hi-C procedure with a conventional chromatin immunoprecipitation assay. However, these methods are time-consuming and require independent methods for validation.

RESULTS

To simultaneously identify protein-centric chromatin conformation and target protein localization, we have developed Cut-C, a method that combines antibody-mediated cleavage by tethered nuclease with chromosome conformation capture to identify chromatin interactions mediated by a protein of interest. Applying Cut-C to H3K4me3, a histone modification enriched at active gene promoters, we have successfully identified chromatin loops mediated by H3K4me3 along with the genome-wide distribution of H3K4me3. Cut-C also identified chromatin loops mediated by CTCF, validating the general applicability of the method.

CONCLUSIONS

Cut-C identifies protein-centric chromatin conformations along with the genome-wide distribution of target proteins using simple procedures. The simplified protocol will improve the efficiency of analysing chromatin conformation using precious materials, such as clinical samples.

摘要

背景

解析基因组的 3D 结构对于详细阐明基因表达的调控机制至关重要。现有的方法,如染色体构象捕获(3C)和 Hi-C,已经能够识别染色质结构的新方面。通过将 Hi-C 程序与传统的染色质免疫沉淀分析相结合,可以进一步识别以蛋白质为中心的染色质构象。然而,这些方法既耗时又需要独立的方法进行验证。

结果

为了同时鉴定以蛋白质为中心的染色质构象和靶蛋白定位,我们开发了 Cut-C 方法,该方法将连接的核酸酶介导的抗体切割与染色体构象捕获相结合,以鉴定由感兴趣的蛋白质介导的染色质相互作用。将 Cut-C 应用于 H3K4me3,一种在活性基因启动子处富集的组蛋白修饰,我们成功地鉴定了 H3K4me3 介导的染色质环以及 H3K4me3 的全基因组分布。Cut-C 还鉴定了 CTCF 介导的染色质环,验证了该方法的通用性。

结论

Cut-C 使用简单的程序鉴定以蛋白质为中心的染色质构象以及靶蛋白的全基因组分布。简化的方案将提高使用珍贵材料(如临床样本)分析染色质构象的效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ade4/6664727/2d756535d614/12864_2019_5989_Fig1_HTML.jpg

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