Multiplexed chromatin immunoprecipitation sequencing for quantitative study of histone modifications and chromatin factors.

IF 13.1 1区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Banushree Kumar, Carmen Navarro, Philip Yuk Kwong Yung, Jing Lyu, Angelo Salazar Mantero, Anna-Maria Katsori, Hannah Schwämmle, Marcel Martin, Simon J Elsässer
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引用次数: 0

Abstract

ChIP-seq is a widely used technique for studying histone post-translational modifications and DNA-binding proteins. DNA fragments associated with a specific protein or histone modification epitope are captured by using antibodies, sequenced and mapped to a reference genome. Albeit versatile and popular, performing many parallel ChIP-seq experiments to compare different conditions, replicates and epitopes is laborious, is prone to experimental variation and does not allow quantitative comparisons unless adequate spike-in chromatin is included. We present a detailed protocol for performing and analyzing a multiplexed quantitative chromatin immunoprecipitation-sequencing experiment (MINUTE-ChIP), in which multiple samples are profiled against multiple epitopes in a single workflow. Multiplexing not only dramatically increases the throughput of ChIP-seq experiments (e.g., profiling 12 samples against multiple histone modifications or DNA-binding proteins in a single experiment), but also enables accurate quantitative comparisons. The protocol consists of four parts: sample preparation (i.e., lysis, chromatin fragmentation and barcoding of native or formaldehyde-fixed material), pooling and splitting of the barcoded chromatin into parallel immunoprecipitation reactions, preparation of next-generation sequencing libraries from input and immunoprecipitated DNA and data analysis using our dedicated analysis pipeline. This pipeline autonomously generates quantitatively scaled ChIP-seq tracks for downstream analysis and visualization, alongside necessary quality control indicators. The entire workflow requires basic knowledge in molecular biology and bioinformatics and can be completed in 1 week. MINUTE-ChIP empowers biologists to perform every ChIP-seq experiment with an appropriate number of replicates and control conditions, delivering more statistically robust, exquisitely quantitative and biologically meaningful results.

用于组蛋白修饰和染色质因子定量研究的多重染色质免疫沉淀测序。
ChIP-seq 是一种广泛用于研究组蛋白翻译后修饰和 DNA 结合蛋白的技术。使用抗体捕获与特定蛋白质或组蛋白修饰表位相关的DNA片段,进行测序并映射到参考基因组。尽管ChIP-seq实验用途广泛且广受欢迎,但进行许多平行的ChIP-seq实验以比较不同的条件、复制和表位却很费力,而且容易出现实验变异,除非加入足够的染色质尖峰,否则无法进行定量比较。我们介绍了执行和分析多重染色质免疫沉淀-测序定量实验(MINUTE-ChIP)的详细方案,在该方案中,多个样品在一个工作流程中针对多个表位进行分析。多重化不仅能显著提高 ChIP-seq 实验的通量(例如,在一次实验中针对多种组蛋白修饰或 DNA 结合蛋白对 12 个样本进行分析),还能进行精确的定量比较。该方案由四部分组成:样品制备(即原生或甲醛固定材料的裂解、染色质片段化和条形码)、将条形码染色质汇集并分割成平行的免疫沉淀反应、从输入和免疫沉淀 DNA 中制备下一代测序文库,以及使用我们的专用分析管道进行数据分析。该流水线可自主生成定量的 ChIP-seq 轨道,用于下游分析和可视化,并提供必要的质量控制指标。整个工作流程需要具备分子生物学和生物信息学的基本知识,可在一周内完成。MINUTE-ChIP 使生物学家能够以适当的重复次数和控制条件进行每一次 ChIP-seq 实验,从而获得统计上更可靠、定量上更精确、生物学上更有意义的结果。
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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