系统性红斑狼疮不同疾病阶段核蛋白改变的分子特征。

IF 3.6 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Qinxin Zhang, Yong Xia, Xiaofeng Li, Jie Li, Donge Tang, Yong Dai, Yulan Chen, Jing Du, Ling Ji, Wei Zhang
{"title":"系统性红斑狼疮不同疾病阶段核蛋白改变的分子特征。","authors":"Qinxin Zhang, Yong Xia, Xiaofeng Li, Jie Li, Donge Tang, Yong Dai, Yulan Chen, Jing Du, Ling Ji, Wei Zhang","doi":"10.1021/acs.jproteome.5c00645","DOIUrl":null,"url":null,"abstract":"<p><p>Systemic lupus erythematosus (SLE) is a complex autoimmune disease characterized by immune dysregulation and the production of autoantibodies targeting nuclear components; yet, the molecular mechanisms linking nuclear protein alterations to disease activity remain poorly defined. Here, we performed integrative proteomic and phosphoproteomic analyses of peripheral blood mononuclear cells from 90 healthy individuals and 130 SLE patients, complemented by transcriptomic profiling of 1,461 SLE patients. Our multiomics analysis revealed progressive dysregulation of nuclear proteins, particularly those involved in RNA processing and immune regulation, with distinct subsets associated with remission and active disease states. Phosphoproteomic profiling uncovered dynamic phosphorylation changes, including reduced multisite phosphorylation of FKBP15 and aberrant activation of kinases such as CDK and CK2. Transcriptome-proteome integration highlighted persistent interferon signaling and inflammatory gene expression, while transcription factor (TF) analysis indicated dysregulation of STAT1 and IRF family members. Network analysis identified central hub proteins, such as NPM1 and PARP1, that bridge post-translational modifications with global transcriptional alterations. Collectively, these findings delineate a multilayered regulatory network connecting protein abundance, phosphorylation dynamics, and TF activity, thereby providing mechanistic insights into SLE pathogenesis and suggesting potential biomarkers and therapeutic targets for disease modulation.</p>","PeriodicalId":48,"journal":{"name":"Journal of Proteome Research","volume":" ","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Molecular Signatures of Nuclear Protein Alterations in Systemic Lupus Erythematosus across Disease Stages.\",\"authors\":\"Qinxin Zhang, Yong Xia, Xiaofeng Li, Jie Li, Donge Tang, Yong Dai, Yulan Chen, Jing Du, Ling Ji, Wei Zhang\",\"doi\":\"10.1021/acs.jproteome.5c00645\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Systemic lupus erythematosus (SLE) is a complex autoimmune disease characterized by immune dysregulation and the production of autoantibodies targeting nuclear components; yet, the molecular mechanisms linking nuclear protein alterations to disease activity remain poorly defined. Here, we performed integrative proteomic and phosphoproteomic analyses of peripheral blood mononuclear cells from 90 healthy individuals and 130 SLE patients, complemented by transcriptomic profiling of 1,461 SLE patients. Our multiomics analysis revealed progressive dysregulation of nuclear proteins, particularly those involved in RNA processing and immune regulation, with distinct subsets associated with remission and active disease states. Phosphoproteomic profiling uncovered dynamic phosphorylation changes, including reduced multisite phosphorylation of FKBP15 and aberrant activation of kinases such as CDK and CK2. Transcriptome-proteome integration highlighted persistent interferon signaling and inflammatory gene expression, while transcription factor (TF) analysis indicated dysregulation of STAT1 and IRF family members. Network analysis identified central hub proteins, such as NPM1 and PARP1, that bridge post-translational modifications with global transcriptional alterations. Collectively, these findings delineate a multilayered regulatory network connecting protein abundance, phosphorylation dynamics, and TF activity, thereby providing mechanistic insights into SLE pathogenesis and suggesting potential biomarkers and therapeutic targets for disease modulation.</p>\",\"PeriodicalId\":48,\"journal\":{\"name\":\"Journal of Proteome Research\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-10-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Proteome Research\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.jproteome.5c00645\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Proteome Research","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1021/acs.jproteome.5c00645","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

摘要

系统性红斑狼疮(SLE)是一种复杂的自身免疫性疾病,其特征是免疫失调和产生针对核成分的自身抗体;然而,将核蛋白改变与疾病活动联系起来的分子机制仍然不明确。在这里,我们对90名健康个体和130名SLE患者的外周血单个核细胞进行了综合蛋白质组学和磷酸化蛋白质组学分析,并对1461名SLE患者进行了转录组学分析。我们的多组学分析揭示了核蛋白的进行性失调,特别是那些参与RNA加工和免疫调节的核蛋白,具有与缓解和活动性疾病状态相关的不同亚群。磷酸化蛋白质组学分析揭示了动态磷酸化的变化,包括FKBP15多位点磷酸化的减少和激酶如CDK和CK2的异常激活。转录组-蛋白质组整合强调了持续的干扰素信号和炎症基因表达,而转录因子(TF)分析表明STAT1和IRF家族成员的失调。网络分析确定了中心枢纽蛋白,如NPM1和PARP1,它们将翻译后修饰与全局转录改变联系起来。总的来说,这些发现描绘了一个多层调节网络,连接蛋白质丰度、磷酸化动力学和TF活性,从而为SLE发病机制提供了机制见解,并提出了疾病调节的潜在生物标志物和治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Signatures of Nuclear Protein Alterations in Systemic Lupus Erythematosus across Disease Stages.

Systemic lupus erythematosus (SLE) is a complex autoimmune disease characterized by immune dysregulation and the production of autoantibodies targeting nuclear components; yet, the molecular mechanisms linking nuclear protein alterations to disease activity remain poorly defined. Here, we performed integrative proteomic and phosphoproteomic analyses of peripheral blood mononuclear cells from 90 healthy individuals and 130 SLE patients, complemented by transcriptomic profiling of 1,461 SLE patients. Our multiomics analysis revealed progressive dysregulation of nuclear proteins, particularly those involved in RNA processing and immune regulation, with distinct subsets associated with remission and active disease states. Phosphoproteomic profiling uncovered dynamic phosphorylation changes, including reduced multisite phosphorylation of FKBP15 and aberrant activation of kinases such as CDK and CK2. Transcriptome-proteome integration highlighted persistent interferon signaling and inflammatory gene expression, while transcription factor (TF) analysis indicated dysregulation of STAT1 and IRF family members. Network analysis identified central hub proteins, such as NPM1 and PARP1, that bridge post-translational modifications with global transcriptional alterations. Collectively, these findings delineate a multilayered regulatory network connecting protein abundance, phosphorylation dynamics, and TF activity, thereby providing mechanistic insights into SLE pathogenesis and suggesting potential biomarkers and therapeutic targets for disease modulation.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Proteome Research
Journal of Proteome Research 生物-生化研究方法
CiteScore
9.00
自引率
4.50%
发文量
251
审稿时长
3 months
期刊介绍: Journal of Proteome Research publishes content encompassing all aspects of global protein analysis and function, including the dynamic aspects of genomics, spatio-temporal proteomics, metabonomics and metabolomics, clinical and agricultural proteomics, as well as advances in methodology including bioinformatics. The theme and emphasis is on a multidisciplinary approach to the life sciences through the synergy between the different types of "omics".
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信