Coiled coil cytoskeletons collaborate in polar growth of Streptomyces.

Bioarchitecture Pub Date : 2013-07-01 DOI:10.4161/bioa.26194
Nora Ausmees
{"title":"Coiled coil cytoskeletons collaborate in polar growth of Streptomyces.","authors":"Nora Ausmees","doi":"10.4161/bioa.26194","DOIUrl":null,"url":null,"abstract":"<p><p>Streptomyces is a multicellular mycelial bacterium, which exhibits pronounced cell polarity and grows by extension of the hyphal tips. Similarly to other polarly growing walled cells, such as filamentous fungi or pollen tubes, Streptomyces hyphae face an intrinsic problem: addition of new cell wall material causes structural weakness of the elongating tip. Cellular strategies employed by walled cells to cope with this problem are not well understood. We have identified a coiled coil protein FilP, with properties similar to those of animal intermediate filament (IF) proteins, which somehow confers rigidity and elasticity to the Streptomyces hyphae. In a recent publication we showed that FilP forms extensive cis-interconnected networks, which likely explain its biological function in determining the mechanical properties of the cells. Surprisingly, the intrinsically non-dynamic cytoskeletal network of FilP exhibits a dynamic behavior in vivo and assembles into growth-dependent polar gradients. We show that apical accumulation of FilP is dependent on its interaction with the main component of the Streptomyces polarisome, DivIVA. Thus, the same polarisome complex that orchestrates cell elongation, also recruits an additional stress-bearing structure to the growing tips with an intrinsically weak cell wall. Similar strategy might be used by all polarly growing walled cells.</p>","PeriodicalId":89329,"journal":{"name":"Bioarchitecture","volume":"3 4","pages":"110-2"},"PeriodicalIF":0.0000,"publicationDate":"2013-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4161/bioa.26194","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioarchitecture","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4161/bioa.26194","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

Abstract

Streptomyces is a multicellular mycelial bacterium, which exhibits pronounced cell polarity and grows by extension of the hyphal tips. Similarly to other polarly growing walled cells, such as filamentous fungi or pollen tubes, Streptomyces hyphae face an intrinsic problem: addition of new cell wall material causes structural weakness of the elongating tip. Cellular strategies employed by walled cells to cope with this problem are not well understood. We have identified a coiled coil protein FilP, with properties similar to those of animal intermediate filament (IF) proteins, which somehow confers rigidity and elasticity to the Streptomyces hyphae. In a recent publication we showed that FilP forms extensive cis-interconnected networks, which likely explain its biological function in determining the mechanical properties of the cells. Surprisingly, the intrinsically non-dynamic cytoskeletal network of FilP exhibits a dynamic behavior in vivo and assembles into growth-dependent polar gradients. We show that apical accumulation of FilP is dependent on its interaction with the main component of the Streptomyces polarisome, DivIVA. Thus, the same polarisome complex that orchestrates cell elongation, also recruits an additional stress-bearing structure to the growing tips with an intrinsically weak cell wall. Similar strategy might be used by all polarly growing walled cells.

螺旋状细胞骨架在链霉菌的极性生长中协同作用。
链霉菌是一种多细胞菌丝体细菌,具有明显的细胞极性,通过菌丝尖端的延伸生长。与其他极性生长的细胞壁细胞(如丝状真菌或花粉管)类似,链霉菌菌丝面临一个内在的问题:添加新的细胞壁材料会导致伸长的尖端结构薄弱。有壁细胞应对这一问题的细胞策略尚不清楚。我们已经鉴定出一种卷曲卷曲的蛋白FilP,具有类似于动物中间丝(IF)蛋白的特性,它以某种方式赋予链霉菌菌丝刚性和弹性。在最近发表的一篇文章中,我们发现FilP形成了广泛的顺式互联网络,这可能解释了它在决定细胞力学特性方面的生物学功能。令人惊讶的是,本质上非动态的FilP细胞骨架网络在体内表现出动态行为,并组装成生长依赖的极性梯度。我们发现FilP的顶端积累依赖于它与极性链霉菌的主要成分DivIVA的相互作用。因此,协调细胞伸长的极化体复合体也为具有本质上薄弱细胞壁的生长尖端招募了额外的应力承受结构。类似的策略可能适用于所有极性生长的壁细胞。
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
自引率
0.00%
发文量
0
×
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:481959085
Book学术官方微信