Roles of transcription factors and chromatin remodelers in regulating innate immune responses in Caenorhabditis elegans.

IF 11.8 1区 生物学 Q1 MICROBIOLOGY
Microbiology and Molecular Biology Reviews Pub Date : 2026-06-25 Epub Date: 2026-05-13 DOI:10.1128/mmbr.00170-25
Paaramitha S Warushavithana, Dustin T Howard, Jordan D West, Vladimir Lažetić
{"title":"Roles of transcription factors and chromatin remodelers in regulating innate immune responses in <i>Caenorhabditis elegans</i>.","authors":"Paaramitha S Warushavithana, Dustin T Howard, Jordan D West, Vladimir Lažetić","doi":"10.1128/mmbr.00170-25","DOIUrl":null,"url":null,"abstract":"<p><p>SUMMARYEffective immunity requires the ability to mount strong pathogen defenses while minimizing detrimental effects on organismal fitness. To achieve this balance, many immune genes are maintained in a transcriptionally repressed but responsive state, ensuring rapid induction upon infection and timely repression once the threat subsides. This dynamic regulation is controlled by transcription factors and chromatin remodelers that fine-tune the accessibility of immune loci. The nematode <i>Caenorhabditis elegans</i> provides a powerful model for dissecting these mechanisms in non-professional immune cells. Its antiviral RNA interference (RNAi) pathway serves as a rapid, sequence-specific silencing system targeting viral RNA. Complementing RNAi, the intracellular pathogen response represents a specialized, inducible transcriptional program that protects <i>C. elegans</i> from intracellular pathogens, including viruses and microsporidia. In addition, pathways regulated by STAT family transcription factors coordinate immune activation in a pathogen- and tissue-specific manner, providing further regulatory diversity. This review explores how transcriptional and chromatin mechanisms coordinate these distinct immune programs to maintain effective yet balanced immune responses. Investigating these pathways in <i>C. elegans</i> continues to uncover both conserved and novel principles of immune regulation, offering insight into how organisms integrate transcriptional control with physiological constraints to thrive in a pathogen-rich environment.</p>","PeriodicalId":18520,"journal":{"name":"Microbiology and Molecular Biology Reviews","volume":" ","pages":"e0017025"},"PeriodicalIF":11.8000,"publicationDate":"2026-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13296363/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiology and Molecular Biology Reviews","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/mmbr.00170-25","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/5/13 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

SUMMARYEffective immunity requires the ability to mount strong pathogen defenses while minimizing detrimental effects on organismal fitness. To achieve this balance, many immune genes are maintained in a transcriptionally repressed but responsive state, ensuring rapid induction upon infection and timely repression once the threat subsides. This dynamic regulation is controlled by transcription factors and chromatin remodelers that fine-tune the accessibility of immune loci. The nematode Caenorhabditis elegans provides a powerful model for dissecting these mechanisms in non-professional immune cells. Its antiviral RNA interference (RNAi) pathway serves as a rapid, sequence-specific silencing system targeting viral RNA. Complementing RNAi, the intracellular pathogen response represents a specialized, inducible transcriptional program that protects C. elegans from intracellular pathogens, including viruses and microsporidia. In addition, pathways regulated by STAT family transcription factors coordinate immune activation in a pathogen- and tissue-specific manner, providing further regulatory diversity. This review explores how transcriptional and chromatin mechanisms coordinate these distinct immune programs to maintain effective yet balanced immune responses. Investigating these pathways in C. elegans continues to uncover both conserved and novel principles of immune regulation, offering insight into how organisms integrate transcriptional control with physiological constraints to thrive in a pathogen-rich environment.

转录因子和染色质重塑因子在秀丽隐杆线虫先天免疫应答调节中的作用。
有效的免疫需要具备强大的病原体防御能力,同时最大限度地减少对机体适应性的有害影响。为了达到这种平衡,许多免疫基因被维持在转录抑制但有反应的状态,确保在感染时快速诱导,并在威胁消退后及时抑制。这种动态调节是由转录因子和染色质重塑物控制的,它们可以微调免疫位点的可及性。秀丽隐杆线虫为剖析非专业免疫细胞中的这些机制提供了一个强有力的模型。它的抗病毒RNA干扰(RNAi)途径是一种针对病毒RNA的快速、序列特异性沉默系统。作为RNAi的补充,细胞内病原体反应代表了一种特殊的、可诱导的转录程序,可以保护秀丽隐杆线虫免受细胞内病原体(包括病毒和微孢子虫)的侵害。此外,STAT家族转录因子调控的途径以病原体和组织特异性的方式协调免疫激活,提供了进一步的调控多样性。这篇综述探讨了转录和染色质机制如何协调这些不同的免疫程序,以维持有效而平衡的免疫反应。在秀丽隐杆线虫中研究这些途径继续揭示保守的和新的免疫调节原理,为生物体如何将转录控制与生理限制结合起来在富含病原体的环境中茁壮成长提供了见解。
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 求助全文
来源期刊
CiteScore
18.80
自引率
0.80%
发文量
27
期刊介绍: Microbiology and Molecular Biology Reviews (MMBR), a journal that explores the significance and interrelationships of recent discoveries in various microbiology fields, publishes review articles that help both specialists and nonspecialists understand and apply the latest findings in their own research. MMBR covers a wide range of topics in microbiology, including microbial ecology, evolution, parasitology, biotechnology, and immunology. The journal caters to scientists with diverse interests in all areas of microbial science and encompasses viruses, bacteria, archaea, fungi, unicellular eukaryotes, and microbial parasites. MMBR primarily publishes authoritative and critical reviews that push the boundaries of knowledge, appealing to both specialists and generalists. The journal often includes descriptive figures and tables to enhance understanding. Indexed/Abstracted in various databases such as Agricola, BIOSIS Previews, CAB Abstracts, Cambridge Scientific Abstracts, Chemical Abstracts Service, Current Contents- Life Sciences, EMBASE, Food Science and Technology Abstracts, Illustrata, MEDLINE, Science Citation Index Expanded (Web of Science), Summon, and Scopus, among others.
×
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
小红书