Waterborg Jakob H
School of Biological Sciences, University of Missouri, Kansas City, MO 64110, USA.
Biochim Biophys Acta. 2011 Aug;1809(8):353-9. doi: 10.1016/j.bbagrm.2011.02.005.
The study of histone acetylation in plants started with protein purification and sequencing, with gel analysis and the use of radioactive tracers. In alfalfa, acid urea Triton gel electrophoresis and in vivo labeling with tritated acetate and lysine quantified dynamic acetylation of core histones and identified the replication-coupled and -independent expression patterns of the histone H3.1 and H3.2 variants. Pulse-chase analyses demonstrated protein turnover of newly synthesized histone H3.2 and thereby identified the replacement H3 histones of plants which maintain the nucleosome density of transcribed chromatin. Sequence analysis of histone H4 revealed acetylation of lysine 20, a site typically methylated in animals and yeasts. Histone deacetylase inhibitors butyrate and trichostatin A are metabolized in alfalfa, but loss of TSA is slow, allowing its use to induce transient hyperacetylation of histones H2B, H4 and H3. This article is part of a Special Issue entitled: Epigenetic Control of cellular and developmental processes in plants.
植物中组蛋白乙酰化的研究始于蛋白质纯化与测序、凝胶分析以及放射性示踪剂的使用。在苜蓿中,酸性尿素Triton凝胶电泳以及用氚化乙酸盐和赖氨酸进行体内标记,对核心组蛋白的动态乙酰化进行了定量,并确定了组蛋白H3.1和H3.2变体的复制偶联和非偶联表达模式。脉冲追踪分析证明了新合成的组蛋白H3.2的蛋白质周转,从而确定了维持转录染色质核小体密度的植物替代H3组蛋白。组蛋白H4的序列分析揭示了赖氨酸20的乙酰化,该位点在动物和酵母中通常被甲基化。组蛋白脱乙酰酶抑制剂丁酸盐和曲古抑菌素A在苜蓿中被代谢,但曲古抑菌素A的损失较慢,使其能够用于诱导组蛋白H2B、H4和H3的瞬时超乙酰化。本文是名为:植物细胞和发育过程的表观遗传控制的特刊的一部分。