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Global Involvement of Lysine Crotonylation in Protein Modification and Transcription Regulation in Rice

机译:赖氨酸巴豆酰化在水稻蛋白质修饰和转录调控中的全球参与

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摘要

Lysine crotonylation (Kcr) is a newly discovered posttranslational modification (PTM) existing in mammals. A global crotonylome analysis was undertaken in rice (Oryza sativa L. japonica) using high accuracy nano-LC-MS/MS in combination with crotonylated peptide enrichment. A total of 1,265 lysine crotonylation sites were identified on 690 proteins in rice seedlings. Subcellular localization analysis revealed that 51% of the crotonylated proteins identified were localized in chloroplasts. The photosynthesis-associated proteins were also mostly enriched in total crotonylated proteins. In addition, a genomic localization analysis of histone Kcr by ChIP-seq was performed to assess the relevance between histone Kcr and the genome. Of the 10,923 identified peak regions, the majority (86.7%) of the enriched peaks were located in gene body, especially exons. Furthermore, the degree of histone Kcr modification was positively correlated with gene expression in genic regions. Compared with other published histone modification data, the Kcr was co-located with the active histone modifications. Interestingly, histone Kcr-facilitated expression of genes with existing active histone modifications. In addition, 77% of histone Kcr modifications overlapped with DNase hypersensitive sites (DHSs) in intergenic regions of the rice genome and might mark other cis-regulatory DNA elements that are different from IPA1, a transcription activator in rice seedlings. Overall, our results provide a comprehensive understanding of the biological functions of the crotonylome and new active histone modification in transcriptional regulation in plants.
机译:赖氨酸巴豆酰化(Kcr)是哺乳动物中新发现的翻译后修饰(PTM)。使用高精度纳米LC-MS / MS和巴豆酰化肽富集相结合的方法对水稻(Oryza sativa L. japonica)进行了全球巴豆酰化组分析。在水稻幼苗中,在690种蛋白质上共鉴定出1,265个赖氨酸巴豆酰化位点。亚细胞定位分析表明,鉴定出的巴豆酰化蛋白中有51%位于叶绿体中。与光合作用相关的蛋白质也大部分富含总的巴豆酰化蛋白质。另外,通过ChIP-seq进行了组蛋白Kcr的基因组定位分析,以评估组蛋白Kcr与基因组之间的相关性。在确定的10,923个峰区域中,大部分富集峰(86.7%)位于基因体中,尤其是外显子。此外,组蛋白Kcr修饰的程度与基因区域的基因表达呈正相关。与其他已发布的组蛋白修饰数据相比,Kcr与有效的组蛋白修饰位于同一位置。有趣的是,组蛋白Kcr促进了具有现有活性组蛋白修饰的基因的表达。此外,77%的组蛋白Kcr修饰与水稻基因组间区域中的DNase超敏位点(DHS)重叠,并可能标记了与水稻幼苗中的转录激活因子IPA1不同的其他顺式调控DNA元素。总的来说,我们的结果提供了对巴豆的基因组生物学功能和植物转录调控中新的活性组蛋白修饰的全面理解。

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