Histone Acid Extraction and High Throughput Mass Spectrometry to Profile Histone Modifications in Arabidopsis thaliana

组蛋白 染色质免疫沉淀 染色质 拟南芥 拟南芥 计算生物学 组蛋白甲基转移酶 组蛋白密码 生物 化学 核小体 生物化学 突变体 DNA 基因 基因表达 发起人
作者
Ray N. Scheid,James A. Dowell,Dean Sanders,Jianjun Jiang,John M. Denu,Xuehua Zhong
出处
期刊:Current protocols [Wiley]
卷期号:2 (8): e527-e527 被引量:10
标识
DOI:10.1002/cpz1.527
摘要

Abstract Histone post‐translational modifications (PTMs) play important roles in many biological processes, including gene regulation and chromatin dynamics, and are thus of high interest across many fields of biological research. Chromatin immunoprecipitation coupled with sequencing (ChIP‐seq) is a powerful tool to profile histone PTMs in vivo . This method, however, is largely dependent on the specificity and availability of suitable commercial antibodies. While mass spectrometry (MS)–based proteomic approaches to quantitatively measure histone PTMs have been developed in mammals and several other model organisms, such methods are currently not readily available in plants. One major challenge for the implementation of such methods in plants has been the difficulty in isolating sufficient amounts of pure, high‐quality histones, a step rendered difficult by the presence of the cell wall. Here, we developed a high‐yielding histone extraction and purification method optimized for Arabidopsis thaliana that can be used to obtain high‐quality histones for MS. In contrast to other methods used in plants, this approach is relatively simple, and does not require membranes or additional specialized steps, such as gel excision or chromatography, to extract highly purified histones. We also describe methods for producing MS‐ready histone peptides through chemical labeling and digestion. Finally, we describe an optimized method to quantify and analyze the resulting histone PTM data using a modified version of EpiProfile 2.0 for Arabidopsis. In all, the workflow described here can be used to measure changes to histone PTMs resulting from various treatments, stresses, and time courses, as well as in different mutant lines. © 2022 Wiley Periodicals LLC. Basic Protocol 1 : Nuclear isolation and histone acid extraction Basic Protocol 2 : Peptide labeling, digestion, and desalting Basic Protocol 3 : Histone HPLC‐MS/MS and data analysis
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