ARIES domains: functional signaling units of type I interferon responses

IF 4.2 The FEBS journal Pub Date : 2025-02-18 DOI:10.1111/febs.70023
Lauren M. Landau, Jonathan C. Kagan
{"title":"ARIES domains: functional signaling units of type I interferon responses","authors":"Lauren M. Landau,&nbsp;Jonathan C. Kagan","doi":"10.1111/febs.70023","DOIUrl":null,"url":null,"abstract":"<p>The innate immune system relies on a network of signaling proteins classified by shared domains, which serve as functional units that orchestrate inflammatory and host defensive activities. Within type I interferon (IFN) responses, the stimulator of interferon genes protein (STING), mitochondrial antiviral-signaling protein (MAVS), Toll-IL-1 receptor-resistance protein domain-containing adapter-inducing interferon-β (TRIF), Toll-like receptor adapter interacting with SLC15A4 on the lysosome (TASL), insulin receptor tyrosine kinase substrate protein of 53 kDa (IRSp53), and GEM interacting protein (GMIP) utilize a conserved pLxIS motif to recruit IRF family transcription factors. Notably, the pLxIS motif functions within a larger signaling unit, which is referred to here as an Activator of Interferon Expression via a pLxIS motif (ARIES) domain. ARIES domains consist of the pLxIS motif and adjacent kinase activation motifs that together drive IFN responses. This review explores how ARIES domains promote immune responses via shared and distinct signaling mechanisms, protein localization, and regulation of metabolic shifts, underscoring their evolutionary conservation and critical role in host defense.</p>","PeriodicalId":94226,"journal":{"name":"The FEBS journal","volume":"292 22","pages":"5888-5898"},"PeriodicalIF":4.2000,"publicationDate":"2025-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12353150/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The FEBS journal","FirstCategoryId":"1085","ListUrlMain":"https://febs.onlinelibrary.wiley.com/doi/10.1111/febs.70023","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The innate immune system relies on a network of signaling proteins classified by shared domains, which serve as functional units that orchestrate inflammatory and host defensive activities. Within type I interferon (IFN) responses, the stimulator of interferon genes protein (STING), mitochondrial antiviral-signaling protein (MAVS), Toll-IL-1 receptor-resistance protein domain-containing adapter-inducing interferon-β (TRIF), Toll-like receptor adapter interacting with SLC15A4 on the lysosome (TASL), insulin receptor tyrosine kinase substrate protein of 53 kDa (IRSp53), and GEM interacting protein (GMIP) utilize a conserved pLxIS motif to recruit IRF family transcription factors. Notably, the pLxIS motif functions within a larger signaling unit, which is referred to here as an Activator of Interferon Expression via a pLxIS motif (ARIES) domain. ARIES domains consist of the pLxIS motif and adjacent kinase activation motifs that together drive IFN responses. This review explores how ARIES domains promote immune responses via shared and distinct signaling mechanisms, protein localization, and regulation of metabolic shifts, underscoring their evolutionary conservation and critical role in host defense.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
ARIES结构域:I型干扰素应答的功能信号单元。
先天免疫系统依赖于一个由共享结构域分类的信号蛋白网络,它作为协调炎症和宿主防御活动的功能单位。在I型干扰素(IFN)应答中,干扰素基因刺激因子蛋白(STING)、线粒体抗病毒信号蛋白(MAVS)、Toll-IL-1受体-抗性蛋白结构域的适配器诱导干扰素-β (TRIF)、与溶酶体SLC15A4相互作用的toll样受体适配器(TASL)、53 kDa的胰岛素受体酪氨酸激酶底物蛋白(IRSp53)和GEM相互作用蛋白(GMIP)利用保守的pLxIS基序募集IRF家族转录因子。值得注意的是,pLxIS基序在一个更大的信号单元中起作用,该单元通过pLxIS基序(ARIES)结构域被称为干扰素表达的激活因子。白羊座结构域由pLxIS基序和邻近的激酶激活基序组成,它们共同驱动IFN反应。这篇综述探讨了ARIES结构域如何通过共享和独特的信号机制、蛋白质定位和代谢变化调节来促进免疫反应,强调了它们的进化保守性和在宿主防御中的关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Elucidating the catalytic mechanism of a previously undescribed carbohydrate esterase family 7 acetyl xylan esterase (LaCE7A). A new branch of mammalian vitamin B6 metabolism: AKR1C-mediated conversion of pyridoxal to pyridoxine and 4-pyridoxolactone. Structural features of a new class of terpenoid cyclases. Determination of the water network surrounding the type I pilus from Escherichia coli by cryo-electron microscopy. Unveiling the influence of salt concentration on the different stages of the catalytic cycle of a halophilic enzyme.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1