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赖氨酸修饰的串扰的特异性系统分析。

Site-Specific Systematic Analysis of Lysine Modification Crosstalk.

机构信息

Department of Chemistry, Nanchang University, No. 999 Xuefu Road, Nanchang, Honggutan New District, Jiangxi Province, 330031, P. R. China.

Department of Materials and Chemical Engineering, Pingxiang University, Pingxiang, P. R. China.

出版信息

Proteomics. 2018 May;18(9):e1700292. doi: 10.1002/pmic.201700292. Epub 2018 Apr 16.

DOI:10.1002/pmic.201700292
PMID:29520963
Abstract

Research has revealed that post-translational modifications (PTMs) that occur at lysine (PLMs) can cooperatively regulate various biological processes by crosstalk. However, the trend of the crosstalk between multiple PLMs and the properties of PLM crosstalk require additional investigation. Here, the crosstalk among acetylation, succinylation, and SUMOylation is systematically studied in a site-specific waz. First, crosstalk between SUMOylation is detected and succinylation is found to be underexpressed, whereas succinylation tends to crosstalk with acetylation and SUMOylation on the same lysine residue while PLM crosstalk is tissue-specific across different species. Further analysis reveals that different PLMs tend to occur crosstalk at diverse subcellular compartments and structural regions, and they participate in distinct biological processes and functions. Additionally, short-term evolutionary analysis shows that there is no additional evolutionary pressure on PLMs crosstalk sites, as found by comparison with singly modified sites. Finally, phylogenetic classification reveals that genes with co-occupied lysine crosstalk are more likely to have higher evolutionary similarity and possess a tendency to cluster in the specific branch. The integrated approach reported here has the potential for large-scale prioritization of in situ crosstalk of PLM candidates and provides a profound understanding of the underlying relationship between different lysine modifications.

摘要

研究表明,赖氨酸(PLM)上发生的翻译后修饰(PTM)可以通过串扰协同调节各种生物过程。然而,多种 PLM 之间串扰的趋势和 PLM 串扰的特性需要进一步研究。在这里,在特定位置系统地研究了乙酰化、琥珀酰化和 SUMO 化之间的串扰。首先,检测到 SUMO 化的串扰,发现琥珀酰化表达不足,而琥珀酰化倾向于与同一赖氨酸残基上的乙酰化和 SUMO 化串扰,而 PLM 串扰在不同物种的不同组织中具有特异性。进一步分析表明,不同的 PLM 倾向于在不同的亚细胞区室和结构区域发生串扰,并且它们参与不同的生物学过程和功能。此外,短期进化分析表明,与单一修饰位点相比,PLM 串扰位点没有额外的进化压力。最后,系统发育分类表明,具有共同占据赖氨酸串扰的基因具有更高的进化相似性,并且倾向于在特定分支中聚类。这里报道的综合方法有可能大规模优先考虑 PLM 候选物的原位串扰,并深入了解不同赖氨酸修饰之间的潜在关系。

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