DNA O-MAP uncovers the molecular neighborhoods associated with specific genomic loci

Yuzhen Liu, Christopher D McGann, Mary Krebs, Thomas A Perkins, Rose Fields, Conor K Camplisson, Chris Hsu, Shayan Avanessian, Ashley F Tsue, Evan E Kania, David M Shechner, Brian J Beliveau, Devin K. Schweppe
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Abstract

The accuracy of crucial nuclear processes such as transcription, replication, and repair, depends on the local composition of chromatin and the regulatory proteins that reside there. Understanding these DNA-protein interactions at the level of specific genomic loci has remained challenging due to technical limitations. Here, we introduce a method termed "DNA O-MAP", which uses programmable peroxidase-conjugated oligonucleotide probes to biotinylate nearby proteins. We show that DNA O-MAP can be coupled with sample multiplexed quantitative proteomics and next-generation sequencing to quantify DNA-protein and DNA-DNA interactions at specific genomic loci.
DNA O-MAP 发现与特定基因组位点相关的分子邻域
转录、复制和修复等关键核过程的准确性取决于染色质的局部组成和其中的调控蛋白。由于技术上的限制,在特定基因组位点水平上理解这些 DNA 蛋白相互作用仍然具有挑战性。在这里,我们介绍了一种被称为 "DNA O-MAP "的方法,它使用可编程过氧化物酶连接的寡核苷酸探针对附近的蛋白质进行生物素化。我们的研究表明,DNA O-MAP可与样本多重定量蛋白质组学和下一代测序相结合,对特定基因组位点的DNA-蛋白质和DNA-DNA相互作用进行定量分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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