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Genome-wide profiling of histone H3 lysine 9 acetylation and dimethylation in Arabidopsis reveals correlation between multiple histone marks and gene expression

机译:拟南芥中组蛋白H3赖氨酸9乙酰化和二甲基化的全基因组分析揭示了多个组蛋白标记与基因表达之间的相关性

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Lysine residue 9 of histone H3 can either be acetylated or mono-, di-, or tri-methylated. These epigenetic states have a diverse impact on regulating gene transcriptional activity and chromatin organization. H3K9ac is invariably correlated with transcriptional activation, whereas H3K9me2 has been reported to be mainly located in constitutive heterochromatin in Arabidopsis. Here, we present epigenetic landscapes for histone H3 lysine 9 acetylation (H3K9ac) and dimethylation (H3K9me2) in Arabidopsis seedlings. The results show that H3K9ac targeted 5,206 non-transposable element (non-TE) genes and 321 transposable elements (TEs), whereas H3K9me2 targeted 2,281 TEs and 1,112 non-TE genes. H3K9ac was biased towards the 5' end of genes and peaked at the ATG position, while H3K9me2 tended to span the entire gene body. H3K9ac correlated with high gene expression, while H3K9me2 correlated with low expression. Analyses of H3K9ac and H3K9me2 with the available datasets of H3K27me3 and DNA methylation revealed a correlation between the occurrence of multiple epigenetic modifications and gene expression. Genes with H3K9ac alone were actively transcribed, while genes that were also modified by either H3K27me3 or DNA methylation showed a lower expression level, suggesting that a combination of repressive marks weakened the positive regulatory effect of H3K9ac. Furthermore, we observed a significant increase of the H3K9ac modification level of selected target genes in hda19 (histone deacetylase 19) mutant seedlings, which indicated that HDA19 plays an important role in regulating the level of H3K9ac and thereby influencing the transcriptional activity in young seedlings.
机译:组蛋白H3的赖氨酸残基9可以被乙酰化或被单,二或三甲基化。这些表观遗传状态对调节基因转录活性和染色质组织具有不同的影响。 H3K9ac总是与转录激活相关,而据报道,H3K9me2主要位于拟南芥中的组成型异染色质中。在这里,我们介绍拟南芥幼苗中组蛋白H3赖氨酸9乙酰化(H3K9ac)和二甲基化(H3K9me2)的表观遗传景观。结果表明,H3K9ac靶向5,206个非转座元件(non-TE)基因和321个转座元件(TEs),而H3K9me2靶向2,281个TEs和1,112个非TE基因。 H3K9ac偏向基因的5'端并在ATG位置达到峰值,而H3K9me2则倾向于跨越整个基因体。 H3K9ac与高基因表达相关,而H3K9me2与低基因表达相关。使用可用的H3K27me3和DNA甲基化数据集对H3K9ac和H3K9me2进行分析,揭示了多种表观遗传修饰的发生与基因表达之间的相关性。单独转录具有H3K9ac的基因,同时也被H3K27me3或DNA甲基化修饰的基因显示较低的表达水平,表明抑制标记的组合削弱了H3K9ac的正调控作用。此外,我们观察到hda19(组蛋白去乙酰化酶19)突变苗中选定目标基因的H3K9ac修饰水平显着增加,这表明HDA19在调节H3K9ac的水平方面具有重要作用,从而影响幼苗的转录活性。

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