Evolution of a large periplasmic disk in Campylobacterota flagella enables both efficient motility and autoagglutination

IF 10.7 1区 生物学 Q1 CELL BIOLOGY Developmental cell Pub Date : 2024-10-02 DOI:10.1016/j.devcel.2024.09.008
Eli J. Cohen, Tina Drobnič, Deborah A. Ribardo, Aoba Yoshioka, Trishant Umrekar, Xuefei Guo, Jose-Jesus Fernandez, Emma E. Brock, Laurence Wilson, Daisuke Nakane, David R. Hendrixson, Morgan Beeby
{"title":"Evolution of a large periplasmic disk in Campylobacterota flagella enables both efficient motility and autoagglutination","authors":"Eli J. Cohen, Tina Drobnič, Deborah A. Ribardo, Aoba Yoshioka, Trishant Umrekar, Xuefei Guo, Jose-Jesus Fernandez, Emma E. Brock, Laurence Wilson, Daisuke Nakane, David R. Hendrixson, Morgan Beeby","doi":"10.1016/j.devcel.2024.09.008","DOIUrl":null,"url":null,"abstract":"The flagellar motors of <em>Campylobacter jejuni</em> (<em>C. jejuni</em>) and related Campylobacterota (previously epsilonproteobacteria) feature 100-nm-wide periplasmic “basal disks” that have been implicated in scaffolding a wider ring of additional motor proteins to increase torque, but the size of these disks is excessive for a role solely in scaffolding motor proteins. Here, we show that the basal disk is a flange that braces the flagellar motor during disentanglement of its flagellar filament from interactions with the cell body and other filaments. We show that motor output is unaffected when we shrink or displace the basal disk, and suppressor mutations of debilitated motors occur in flagellar-filament or cell-surface glycosylation pathways, thus sidestepping the need for a flange to overcome the interactions between two flagellar filaments and between flagellar filaments and the cell body. Our results identify unanticipated co-dependencies in the evolution of flagellar motor structure and cell-surface properties in the Campylobacterota.","PeriodicalId":11157,"journal":{"name":"Developmental cell","volume":"8 1","pages":""},"PeriodicalIF":10.7000,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental cell","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.devcel.2024.09.008","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The flagellar motors of Campylobacter jejuni (C. jejuni) and related Campylobacterota (previously epsilonproteobacteria) feature 100-nm-wide periplasmic “basal disks” that have been implicated in scaffolding a wider ring of additional motor proteins to increase torque, but the size of these disks is excessive for a role solely in scaffolding motor proteins. Here, we show that the basal disk is a flange that braces the flagellar motor during disentanglement of its flagellar filament from interactions with the cell body and other filaments. We show that motor output is unaffected when we shrink or displace the basal disk, and suppressor mutations of debilitated motors occur in flagellar-filament or cell-surface glycosylation pathways, thus sidestepping the need for a flange to overcome the interactions between two flagellar filaments and between flagellar filaments and the cell body. Our results identify unanticipated co-dependencies in the evolution of flagellar motor structure and cell-surface properties in the Campylobacterota.

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
弯曲杆菌鞭毛中大型周质盘的进化使其既能高效运动又能自动凝集
空肠弯曲杆菌(Campylobacter jejuni)和相关弯曲杆菌属(以前的epsilonproteobacteria)的鞭毛马达具有 100 nm 宽的质膜周围 "基盘",它被认为可为更宽的附加马达蛋白环提供支架以增加扭矩,但这些基盘的尺寸过大,不能仅用于为马达蛋白提供支架。在这里,我们展示了基盘是一个凸缘,在鞭毛运动的鞭毛丝与细胞体和其他丝相互作用时,它支撑着鞭毛运动。我们的研究表明,当我们缩小或移位基盘时,马达的输出不受影响,而且衰弱马达的抑制突变发生在鞭毛丝或细胞表面糖基化途径中,从而避免了需要一个凸缘来克服两个鞭毛丝之间以及鞭毛丝与细胞体之间的相互作用。我们的研究结果确定了弯曲杆菌群中鞭毛马达结构和细胞表面特性进化过程中意想不到的共同依赖性。
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
Developmental cell
Developmental cell 生物-发育生物学
CiteScore
18.90
自引率
1.70%
发文量
203
审稿时长
3-6 weeks
期刊介绍: Developmental Cell, established in 2001, is a comprehensive journal that explores a wide range of topics in cell and developmental biology. Our publication encompasses work across various disciplines within biology, with a particular emphasis on investigating the intersections between cell biology, developmental biology, and other related fields. Our primary objective is to present research conducted through a cell biological perspective, addressing the essential mechanisms governing cell function, cellular interactions, and responses to the environment. Moreover, we focus on understanding the collective behavior of cells, culminating in the formation of tissues, organs, and whole organisms, while also investigating the consequences of any malfunctions in these intricate processes.
期刊最新文献
The vertebrate segmentation clock drives segmentation by stabilizing Dusp phosphatases in zebrafish Adeno-associated viral tools to trace neural development and connectivity across amphibians Self-organized pattern formation in the developing mouse neural tube by a temporal relay of BMP signaling Development of an inducible DNA barcoding system to understand lineage changes in Arabidopsis regeneration Gene module reconstruction identifies cellular differentiation processes and the regulatory logic of specialized secretion in zebrafish
×
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:481959085
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