Profiling large-scale protein occupancy on bacterial genomes using IPOD-HR.

IF 16 1区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Rebecca L Hurto, Jeremy W Schroeder, Julian Trouillon, Uwe Sauer, Lydia Freddolino
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引用次数: 0

Abstract

Identifying genomic regions bound by individual proteins such as transcription factors is essential to understanding bacterial gene regulation; however, comprehensive understanding of the effect of protein occupancy on gene regulation would be prohibitively laborious and expensive to achieve using methods such as chromatin immunoprecipitation with sequencing (ChIP-seq) and ChIP with exonuclease treatment (ChIP-exo) for every protein and condition of interest. Here we describe a protocol for performing in vivo protein occupancy display-high resolution (IPOD-HR), a powerful method for genome-wide profiling of protein-bound DNA in prokaryotic systems. Although assay for transposase-accessible chromatin with sequencing (ATAC-seq) is the method of choice for assaying general protein occupancy in eukaryotic systems, bacterial nucleoid-associated proteins can affect ATAC-seq, rendering it unsuitable for use in bacteria. In contrast, IPOD-HR can be used to identify regions of bacterial genomes that are highly bound by proteins, regardless of the identity of the proteins bound, allowing the identification of condition- and genotype-dependent changes in protein occupancy associated with changes in gene regulation. The technique is coupled to RNA polymerase ChIP, followed by sequencing of the extracted samples and downstream analysis using open-source, automated software that we provide and actively maintain. Once cross-linked samples are obtained, the core DNA selection portion of the IPOD-HR protocol takes 3 calendar days to perform. The resulting DNA extracts are subjected to high-throughput sequencing, resulting in sequencing data that are analyzed, which typically requires a few additional days, depending on the number of samples and computing resources. The IPOD-HR experimental method requires familiarity with standard molecular biology techniques suitable for preparing Illumina sequencing inputs, and the computational post-processing pipeline requires basic knowledge of the Linux command line environment.

利用IPOD-HR分析细菌基因组上的大规模蛋白质占用。
鉴定由转录因子等单个蛋白质结合的基因组区域对于理解细菌基因调控至关重要;然而,要全面了解蛋白质占用对基因调控的影响,使用染色质免疫沉淀测序(ChIP-seq)和ChIP外切酶处理(ChIP-exo)等方法对每个蛋白质和感兴趣的条件进行测序是非常费力和昂贵的。在这里,我们描述了一种执行体内蛋白质占用显示高分辨率(IPOD-HR)的方案,这是一种在原核系统中对蛋白质结合DNA进行全基因组分析的强大方法。虽然转座酶可及染色质测序法(ATAC-seq)是测定真核系统中一般蛋白质占用率的首选方法,但细菌核相关蛋白会影响ATAC-seq,使其不适合用于细菌。相比之下,IPOD-HR可用于鉴定细菌基因组中与蛋白质高度结合的区域,而不考虑结合蛋白质的身份,从而鉴定与基因调控变化相关的蛋白质占用的条件和基因型依赖性变化。该技术与RNA聚合酶ChIP相结合,然后使用我们提供并积极维护的开源自动化软件对提取的样品进行测序和下游分析。一旦获得交联样本,IPOD-HR协议的核心DNA选择部分需要3个日历天才能完成。所得到的DNA提取物要进行高通量测序,从而分析测序数据,这通常需要几天的额外时间,具体取决于样品的数量和计算资源。IPOD-HR实验方法需要熟悉适用于制备Illumina测序输入的标准分子生物学技术,计算后处理管道需要Linux命令行环境的基本知识。
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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来源期刊
Nature Protocols
Nature Protocols 生物-生化研究方法
CiteScore
29.10
自引率
0.70%
发文量
128
审稿时长
4 months
期刊介绍: Nature Protocols focuses on publishing protocols used to address significant biological and biomedical science research questions, including methods grounded in physics and chemistry with practical applications to biological problems. The journal caters to a primary audience of research scientists and, as such, exclusively publishes protocols with research applications. Protocols primarily aimed at influencing patient management and treatment decisions are not featured. The specific techniques covered encompass a wide range, including but not limited to: Biochemistry, Cell biology, Cell culture, Chemical modification, Computational biology, Developmental biology, Epigenomics, Genetic analysis, Genetic modification, Genomics, Imaging, Immunology, Isolation, purification, and separation, Lipidomics, Metabolomics, Microbiology, Model organisms, Nanotechnology, Neuroscience, Nucleic-acid-based molecular biology, Pharmacology, Plant biology, Protein analysis, Proteomics, Spectroscopy, Structural biology, Synthetic chemistry, Tissue culture, Toxicology, and Virology.
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