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拟南芥中组蛋白变体和翻译后修饰的串联质谱定量分析。

Quantitative Profiling of Histone Variants and Posttranslational Modifications by Tandem Mass Spectrometry in Arabidopsis.

机构信息

Grenoble Alpes University-CNRS-INRAE-CEA, Plant and Cell Physiology Lab (LPCV), IRIG-DBSCI, Grenoble, France.

University Grenoble Alpes, CEA, INSERM, UA13 BGE, CNRS, CEA, FR2048, Grenoble, France.

出版信息

Methods Mol Biol. 2025;2873:19-38. doi: 10.1007/978-1-0716-4228-3_2.

Abstract

Histone dynamics constitute an important layer of gene regulations associated with development and growth in multicellular eukaryotes. They also stand as key determinants of plant responses to environmental changes. Histone dynamics include the exchange of histone variants as well as post-translational modifications of their amino acid residues (such as acetylation and mono/di/trimethylation), commonly referred to as histone marks. Investigating histone dynamics with a focus on combinatorial changes occurring at their residues will greatly help unravel how plants achieve phenotypic plasticity.Mass spectrometry (MS) analysis offers unequaled resolution of the abundance of histone variants and of their marks. Indeed, relative to other techniques such as western blot or genome-wide profiling, this powerful technique allows quantifying the relative abundances of histone forms, as well as revealing coexisting marks on the same histone molecule. Yet, while MS-based histone analysis has proven efficient in several animals and other model organisms, this method stands out as more challenging in plants. One major challenge is the isolation of sufficient amounts of pure, high-quality histones, likely rendered difficult by the presence of the cell wall, for sufficiently deep and resolutive identification of histone species.In this chapter, we describe a straightforward MS-based proteomic method, implemented to characterize histone marks from Arabidopsis thaliana seedling tissues and cell culture suspensions. After acid extraction of histones, in vitro propionylation of free lysine residues, and digestion with trypsin, a treatment at highly basic pH allows obtaining sharp spectral signals of biologically relevant histone peptide forms.The method workflow described here shall be used to measure changes in histone marks between Arabidopsis thaliana genotypes, along developmental time-courses, or upon various stresses and treatments.

摘要

组蛋白动力学构成了与多细胞真核生物发育和生长相关的基因调控的重要层次。它们也是植物对环境变化响应的关键决定因素。组蛋白动力学包括组蛋白变体的交换以及其氨基酸残基的翻译后修饰(如乙酰化和单/二/三甲基化),通常称为组蛋白标记。重点研究组蛋白动力学及其残基上发生的组合变化,将极大地帮助我们了解植物如何实现表型可塑性。

质谱 (MS) 分析提供了无与伦比的分辨率,可用于研究组蛋白变体及其标记的丰度。事实上,与其他技术(如 Western blot 或全基因组分析)相比,这种强大的技术不仅可以定量组蛋白形式的相对丰度,还可以揭示同一组蛋白分子上共存的标记。然而,虽然基于 MS 的组蛋白分析已在几种动物和其他模式生物中得到证实,但该方法在植物中更具挑战性。一个主要的挑战是分离足够数量的纯、高质量的组蛋白,由于细胞壁的存在,这可能使组蛋白形式的充分深入和分辨率识别变得困难。

在本章中,我们描述了一种直接的基于 MS 的蛋白质组学方法,用于鉴定拟南芥幼苗组织和细胞培养悬浮液中的组蛋白标记。组蛋白经酸提取、体外赖氨酸残基丙酰化和胰蛋白酶消化后,在高碱性 pH 值下处理可获得生物相关组蛋白肽形式的尖锐光谱信号。

此处描述的方法工作流程将用于测量拟南芥不同基因型、发育时间过程或各种胁迫和处理之间组蛋白标记的变化。

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