Abstract
Covalent modifications of histone-tail amino acid residues communicate information via a specific 'histone code'. Here, we report histone H3-tail lysine methylation profiles of several Arabidopsis genes in correlation with their transcriptional activity and the input of the epigenetic factor ARABIDOPSIS HOMOLOG OF TRITHORAX (ATX1) at ATX1-regulated loci. By chromatin immunoprecipitation (ChIP) assays, we compared modification patterns of a constitutively expressed housekeeping gene, of a tissue-specific gene, and among genes that differed in degrees of transcriptional activity. Our results suggest that the di-methylated isoform of histone H3-lysine4 (m2K4/H3) provide a general mark for gene-related sequences distinguishing them from non-transcribed regions. Lys-4 (K4/H3), lys-9 (K9/H3) and lys-27 (K27/H3) nucleosome methylation patterns of plant genes may be gene-, tissue- or development-regulated. Absence of nucleosomes from the LTP-promotor was not sufficient to provoke robust transcription in mutant atx1-leaf chromatin, suggesting that the mechanism repositioning nucleosomes at transition to flowering functioned independently of ATX1.
MeSH Terms
Arabidopsis/genetics,metabolism
Arabidopsis Proteins/genetics,physiology
Chromatin/metabolism
Gene Expression Regulation, Plant
Histone-Lysine N-Methyltransferase
Histones/chemistry,metabolism
Lysine/metabolism
Methylation
Mutation
Nucleosomes/metabolism
Plant Leaves/genetics,metabolism
Promoter Regions, Genetic
Transcription Factors/genetics,physiology
Transcription, Genetic
Chemicals
Arabidopsis Proteins
Chromatin
Histones
Nucleosomes
Transcription Factors
At2g31650 protein, Arabidopsis
Histone-Lysine N-Methyltransferase
Lysine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Alvarez-Venegas Raul
School of Biological Sciences, UNL, Lincoln, NE 68588-011, USA.
Avramova Zoya
References (28)
28 references, click to expand
-
Targeted recruitment of Set1 histone methylase by elongating Pol II provides a localized mark and memory of recent transcriptional activity.
Mol Cell. 2003 Mar;11(3):709-19
PMID: 12667453
-
ATX-1, an Arabidopsis homolog of trithorax, activates flower homeotic genes.
Curr Biol. 2003 Apr 15;13(8):627-37
PMID: 12699618
-
Histone lysine methylation: a signature for chromatin function.
Trends Genet. 2003 Nov;19(11):629-39
PMID: 14585615
-
Methylation of histone H3 K4 mediates association of the Isw1p ATPase with chromatin.
Mol Cell. 2003 Nov;12(5):1325-32
PMID: 14636589
-
Histone H3 lysine 4 methylation patterns in higher eukaryotic genes.
Nat Cell Biol. 2004 Jan;6(1):73-7
PMID: 14661024
-
Vernalization in Arabidopsis thaliana is mediated by the PHD finger protein VIN3.
Nature. 2004 Jan 8;427(6970):159-64
PMID: 14712276
-
Vernalization requires epigenetic silencing of FLC by histone methylation.
Nature. 2004 Jan 8;427(6970):164-7
PMID: 14712277
-
Dimethylation of histone H3 lysine 9 is a critical mark for DNA methylation and gene silencing in Arabidopsis thaliana.
Chromosoma. 2004 Mar;112(6):308-15
PMID: 15014946
-
A plant dialect of the histone language.
Trends Plant Sci. 2004 Feb;9(2):84-90
PMID: 15102374
-
Distinct localization of histone H3 acetylation and H3-K4 methylation to the transcription start sites in the human genome.
Proc Natl Acad Sci U S A. 2004 May 11;101(19):7357-62
PMID: 15123803
-
DNA and histone methylation in plants.
Trends Genet. 2004 Jun;20(6):244-51
PMID: 15145577
-
The histone modification pattern of active genes revealed through genome-wide chromatin analysis of a higher eukaryote.
Genes Dev. 2004 Jun 1;18(11):1263-71
PMID: 15175259
-
Role of transposable elements in heterochromatin and epigenetic control.
Nature. 2004 Jul 22;430(6998):471-6
PMID: 15269773
-
Dual histone H3 methylation marks at lysines 9 and 27 required for interaction with CHROMOMETHYLASE3.
EMBO J. 2004 Oct 27;23(21):4286-96
PMID: 15457214
-
A DNA methyltransferase homolog with a chromodomain exists in multiple polymorphic forms in Arabidopsis.
Genetics. 1998 May;149(1):307-18
PMID: 9584105
-
Plant defense peptides.
Biopolymers. 1998;47(6):479-91
PMID: 10333739
-
Mass spectrometry analysis of Arabidopsis histone H3 reveals distinct combinations of post-translational modifications.
Nucleic Acids Res. 2004;32(22):6511-8
PMID: 15598823
-
Histone modifications defining active genes persist after transcriptional and mitotic inactivation.
EMBO J. 2005 Jan 26;24(2):347-57
PMID: 15616580
-
Profiling histone modification patterns in plants using genomic tiling microarrays.
Nat Methods. 2005 Mar;2(3):213-8
PMID: 16163802
-
The language of covalent histone modifications.
Nature. 2000 Jan 6;403(6765):41-5
PMID: 10638745
-
Transitions in distinct histone H3 methylation patterns at the heterochromatin domain boundaries.
Science. 2001 Aug 10;293(5532):1150-5
PMID: 11498594
-
The Arabidopsis thaliana genome contains at least 29 active genes encoding SET domain proteins that can be assigned to four evolutionarily conserved classes.
Nucleic Acids Res. 2001 Nov 1;29(21):4319-33
PMID: 11691919
-
Heterochromatin in animals and plants. Similarities and differences.
Plant Physiol. 2002 May;129(1):40-9
PMID: 12011336
-
SET-domain proteins of the Su(var)3-9, E(z) and trithorax families.
Gene. 2002 Feb 20;285(1-2):25-37
PMID: 12039029
-
Methylation of histone H3 Lys 4 in coding regions of active genes.
Proc Natl Acad Sci U S A. 2002 Jun 25;99(13):8695-700
PMID: 12060701
-
Interplay between two epigenetic marks. DNA methylation and histone H3 lysine 9 methylation.
Curr Biol. 2002 Aug 20;12(16):1360-7
PMID: 12194816
-
Active genes are tri-methylated at K4 of histone H3.
Nature. 2002 Sep 26;419(6905):407-11
PMID: 12353038
-
Histone modifications in Arabidopsis- high methylation of H3 lysine 9 is dispensable for constitutive heterochromatin.
Plant J. 2003 Feb;33(3):471-80
PMID: 12581305