Dynamic changes in genome-wide histone H3 lysine 4 methylation patterns in response to dehydration stress in Arabidopsis thaliana

被引:158
|
作者
van Dijk, Karin [1 ,5 ]
Ding, Yong [1 ]
Malkaram, Sridhar [1 ]
Riethoven, Jean-Jack M. [1 ,2 ]
Liu, Rong [1 ,6 ]
Yang, Jingyi [1 ,7 ]
Laczko, Peter [1 ]
Chen, Han [1 ]
Xia, Yuannan [1 ]
Ladunga, Istvan [1 ,3 ]
Avramova, Zoya [2 ]
Fromm, Michael [1 ,4 ]
机构
[1] Univ Nebraska, Ctr Biotechnol, Lincoln, NE 68588 USA
[2] Univ Nebraska, Sch Biol Sci, Lincoln, NE 68588 USA
[3] Univ Nebraska, Dept Stat, Lincoln, NE 68588 USA
[4] Univ Nebraska, Dept Agron & Hort, Lincoln, NE 68583 USA
[5] Creighton Univ, Dept Biol, Omaha, NE 68178 USA
[6] Univ Calif Los Angeles, Dept Biomed Engn, Los Angeles, CA 90095 USA
[7] Microsoft Corp, Redmond, WA 98052 USA
来源
BMC PLANT BIOLOGY | 2010年 / 10卷
基金
美国国家科学基金会;
关键词
GENE-EXPRESSION; CHROMATIN MODIFICATIONS; DNA METHYLATION; INDUCIBLE GENES; PROMOTERS; PROTEIN; ROLES; IDENTIFICATION; ACETYLATION; DATABASE;
D O I
10.1186/1471-2229-10-238
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: The molecular mechanisms of genome reprogramming during transcriptional responses to stress are associated with specific chromatin modifications. Available data, however, describe histone modifications only at individual plant genes induced by stress. We have no knowledge of chromatin modifications taking place at genes whose transcription has been down-regulated or on the genome-wide chromatin modification patterns that occur during the plant's response to dehydration stress. Results: Using chromatin immunoprecipitation and deep sequencing (ChIP-Seq) we established the whole-genome distribution patterns of histone H3 lysine 4 mono-, di-, and tri-methylation (H3K4me1, H3K4me2, and H3K4me3, respectively) in Arabidopsis thaliana during watered and dehydration stress conditions. In contrast to the relatively even distribution of H3 throughout the genome, the H3K4me1, H3K4me2, and H3K4me3 marks are predominantly located on genes. About 90% of annotated genes carry one or more of the H3K4 methylation marks. The H3K4me1 and H3K4me2 marks are more widely distributed (80% and 84%, respectively) than the H3K4me3 marks (62%), but the H3K4me2 and H3K4me1 levels changed only modestly during dehydration stress. By contrast, the H3K4me3 abundance changed robustly when transcripts levels from responding genes increased or decreased. In contrast to the prominent H3K4me3 peaks present at the 5'-ends of most transcribed genes, genes inducible by dehydration and ABA displayed atypically broader H3K4me3 distribution profiles that were present before and after the stress. Conclusions: A higher number (90%) of annotated Arabidopsis genes carry one or more types of H3K4me marks than previously reported. During the response to dehydration stress the changes in H3K4me1, H3K4me2, and H3K4me3 patterns show different dynamics and specific patterns at up-regulated, down-regulated, and unaffected genes. The different behavior of each methylation mark during the response process illustrates that they have distinct roles in the transcriptional response of implicated genes. The broad H3K4me3 distribution profiles on nucleosomes of stress-induced genes uncovered a specific chromatin pattern associated with many of the genes involved in the dehydration stress response.
引用
收藏
页数:12
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