Transcriptional responses to salinity-induced changes in cell wall morphology of the euryhaline diatom Pleurosira laevis

IF 2.8 3区 生物学 Q1 MARINE & FRESHWATER BIOLOGY
Shiho Kamakura, Gust Bilcke, Shinya Sato
{"title":"Transcriptional responses to salinity-induced changes in cell wall morphology of the euryhaline diatom Pleurosira laevis","authors":"Shiho Kamakura,&nbsp;Gust Bilcke,&nbsp;Shinya Sato","doi":"10.1111/jpy.13437","DOIUrl":null,"url":null,"abstract":"<p>Diatoms are unicellular algae with morphologically diverse silica cell walls, which are called frustules. The mechanism of frustule morphogenesis has attracted attention in biology and nanomaterials engineering. However, the genetic regulation of the morphology remains unclear. We therefore used transcriptome sequencing to search for genes involved in frustule morphology in the centric diatom <i>Pleurosira laevis</i>, which exhibits morphological plasticity between flat and domed valve faces in salinity 2 and 7, respectively. We observed differential expression of transposable elements (TEs) and transporters, likely due to osmotic response. Up-regulation of mechanosensitive ion channels and down-regulation of Ca<sup>2+</sup>-ATPases in cells with flat valves suggested that cytosolic Ca<sup>2+</sup> levels were changed between the morphologies. Calcium signaling could be a mechanism for detecting osmotic pressure changes and triggering morphological shifts. We also observed an up-regulation of ARPC1 and annexin, involved in the regulation of actin filament dynamics known to affect frustule morphology, as well as the up-regulation of genes encoding frustule-related proteins such as BacSETs and frustulin. Taken together, we propose a model in which salinity-induced morphogenetic changes are driven by upstream responses, such as the regulation of cytosolic Ca<sup>2+</sup> levels, and downstream responses, such as Ca<sup>2+</sup>-dependent regulation of actin dynamics and frustule-related proteins. This study highlights the sensitivity of euryhaline diatoms to environmental salinity and the role of active cellular processes in controlling gross valve morphology under different osmotic pressures.</p>","PeriodicalId":16831,"journal":{"name":"Journal of Phycology","volume":null,"pages":null},"PeriodicalIF":2.8000,"publicationDate":"2024-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jpy.13437","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Phycology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jpy.13437","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MARINE & FRESHWATER BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Diatoms are unicellular algae with morphologically diverse silica cell walls, which are called frustules. The mechanism of frustule morphogenesis has attracted attention in biology and nanomaterials engineering. However, the genetic regulation of the morphology remains unclear. We therefore used transcriptome sequencing to search for genes involved in frustule morphology in the centric diatom Pleurosira laevis, which exhibits morphological plasticity between flat and domed valve faces in salinity 2 and 7, respectively. We observed differential expression of transposable elements (TEs) and transporters, likely due to osmotic response. Up-regulation of mechanosensitive ion channels and down-regulation of Ca2+-ATPases in cells with flat valves suggested that cytosolic Ca2+ levels were changed between the morphologies. Calcium signaling could be a mechanism for detecting osmotic pressure changes and triggering morphological shifts. We also observed an up-regulation of ARPC1 and annexin, involved in the regulation of actin filament dynamics known to affect frustule morphology, as well as the up-regulation of genes encoding frustule-related proteins such as BacSETs and frustulin. Taken together, we propose a model in which salinity-induced morphogenetic changes are driven by upstream responses, such as the regulation of cytosolic Ca2+ levels, and downstream responses, such as Ca2+-dependent regulation of actin dynamics and frustule-related proteins. This study highlights the sensitivity of euryhaline diatoms to environmental salinity and the role of active cellular processes in controlling gross valve morphology under different osmotic pressures.

Abstract Image

盐度诱导海水硅藻 Pleurosira laevis 细胞壁形态变化的转录反应。
硅藻是一种单细胞藻类,具有形态各异的二氧化硅细胞壁,这种细胞壁被称为 "微囊"。挫折形态发生的机制已引起生物学和纳米材料工程学的关注。然而,这种形态的遗传调控仍不清楚。因此,我们利用转录组测序技术,在中心硅藻 Pleurosira laevis 中寻找参与瓣叶形态的基因,该硅藻在盐度为 2 和 7 时分别表现出扁平瓣面和圆顶瓣面的形态可塑性。我们观察到转座元件(TE)和转运体的不同表达,这可能是由于渗透反应引起的。平瓣细胞中机械敏感离子通道的上调和 Ca2+ -ATP 酶的下调表明,细胞膜 Ca2+ 水平在两种形态之间发生了变化。钙信号转导可能是检测渗透压变化和触发形态转变的一种机制。我们还观察到参与调节肌动蛋白丝动态的 ARPC1 和 annexin 的上调,已知它们会影响突起形态,以及编码突起相关蛋白(如 BacSETs 和 frustulin)的基因的上调。综上所述,我们提出了一个模型,在该模型中,盐度诱导的形态发生变化是由上游反应(如细胞膜 Ca2+ 水平的调节)和下游反应(如依靠 Ca2+ 对肌动蛋白动力学和嵴相关蛋白的调节)驱动的。这项研究强调了极鞭毛硅藻对环境盐度的敏感性,以及在不同渗透压下活性细胞过程在控制总瓣形态中的作用。
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 求助全文
来源期刊
Journal of Phycology
Journal of Phycology 生物-海洋与淡水生物学
CiteScore
6.50
自引率
3.40%
发文量
69
审稿时长
2 months
期刊介绍: The Journal of Phycology was founded in 1965 by the Phycological Society of America. All aspects of basic and applied research on algae are included to provide a common medium for the ecologist, physiologist, cell biologist, molecular biologist, morphologist, oceanographer, taxonomist, geneticist, and biochemist. The Journal also welcomes research that emphasizes algal interactions with other organisms and the roles of algae as components of natural ecosystems. All aspects of basic and applied research on algae are included to provide a common medium for the ecologist, physiologist, cell biologist, molecular biologist, morphologist, oceanographer, acquaculturist, systematist, geneticist, and biochemist. The Journal also welcomes research that emphasizes algal interactions with other organisms and the roles of algae as components of natural ecosystems.
×
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