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野生型和组蛋白去乙酰化酶 1 突变体粗糙脉孢菌中组蛋白 H2B 的广泛而多样的修饰。

Extensive and varied modifications in histone H2B of wild-type and histone deacetylase 1 mutant Neurospora crassa.

机构信息

Institute of Molecular Biology, University of Oregon, Eugene, Oregon 97403, USA.

出版信息

Biochemistry. 2010 Jun 29;49(25):5244-57. doi: 10.1021/bi100391w.

Abstract

DNA methylation is deficient in a histone deacetylase 1 (HDA1) mutant (hda-1) strain of Neurospora crassa with inactivated histone deacetylase 1. Difference two-dimensional (2D) gels identified the primary histone deacetylase 1 target as histone H2B. Acetylation was identified by LC-MS/MS at five different lysines in wild-type H2B and at 11 lysines in hda-1 H2B, suggesting Neurospora H2B is a complex combination of different acetylated species. Individual 2D gel spots were shifted by single lysine acetylations. FTICR MS-observed methylation ladders identify an ensemble of 20-25 or more modified forms for each 2D gel spot. Twelve different lysines or arginines were methylated in H2B from the wild type or hda-1; only two were in the N-terminal tail. Arginines were modified by monomethylation, dimethylation, or deimination. H2B from wild-type and hda-1 ensembles may thus differ by acetylation at multiple sites, and by additional modifications. Combined with asymmetry-generated diversity in H2B structural states in nucleosome core particles, the extensive modifications identified here can create substantial histone-generated structural diversity in nucleosome core particles.

摘要

DNA 甲基化在烟曲霉组蛋白去乙酰化酶 1(HDA1)突变体(hda-1)中缺失,该突变体中组蛋白去乙酰化酶 1 失活。差异二维(2D)凝胶鉴定出主要的组蛋白去乙酰化酶 1 靶标是组蛋白 H2B。通过 LC-MS/MS 在野生型 H2B 的五个不同赖氨酸和 hda-1 H2B 的 11 个赖氨酸上鉴定出乙酰化,这表明 Neurospora H2B 是不同乙酰化物种的复杂组合。单个 2D 凝胶斑点通过单个赖氨酸乙酰化发生位移。FTICR MS 观察到的甲基化梯可以识别每个 2D 凝胶斑点的 20-25 种或更多修饰形式的组合。野生型或 hda-1 的 H2B 中有 12 个不同的赖氨酸或精氨酸被甲基化;只有两个位于 N 端尾部。精氨酸被单甲基化、二甲基化或去氨基化修饰。因此,来自野生型和 hda-1 集合的 H2B 可能在多个位点发生乙酰化,并且具有其他修饰。与核小体核心颗粒中 H2B 结构状态产生的不对称多样性相结合,这里鉴定的广泛修饰可以在核小体核心颗粒中产生大量组蛋白产生的结构多样性。

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