Extensive and Varied Modifications in Histone H2B of Wild-Type and Histone Deacetylase 1 Mutant Neurospora crassa

被引:8
|
作者
Anderson, D. C. [1 ]
Green, George R. [2 ]
Smith, Kristina [1 ]
Selker, Eric U. [1 ]
机构
[1] Univ Oregon, Inst Mol Biol, Eugene, OR 97403 USA
[2] Mercer Univ, Coll Pharm & Hlth Sci, Atlanta, GA 30341 USA
关键词
VECTOR MACHINE CLASSIFICATION; DNA METHYLATION; POSTTRANSLATIONAL MODIFICATIONS; ARGININE METHYLATION; MASS-SPECTROMETRY; PEPTIDYLARGININE DEIMINASE; H3; METHYLTRANSFERASE; PROTEIN; IDENTIFICATION; PHOSPHORYLATION;
D O I
10.1021/bi100391w
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA methylation is deficient in a histone deacetylase 1 (HDA1) mutant (hda-1) strain of Neurospora crassa with inactivated histone deacetylase I. Difference two-dimensional (2D) eels 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 eel 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.
引用
收藏
页码:5244 / 5257
页数:14
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