Binary fission in Trichoplax is orthogonal to the subsequent division plane

IF 2.6 Q2 Medicine
Jorge Zuccolotto-Arellano, Rodrigo Cuervo-González
{"title":"Binary fission in Trichoplax is orthogonal to the subsequent division plane","authors":"Jorge Zuccolotto-Arellano,&nbsp;Rodrigo Cuervo-González","doi":"10.1016/j.mod.2020.103608","DOIUrl":null,"url":null,"abstract":"<div><p>Asexual reproduction in <em>Trichoplax</em> occurs mainly by binary fission and occasionally by the budding of epithelial spheres called “swarmers”. The process that leads to binary fission and the mechanisms involved in this segregation are practically unknown. <em>Trichoplax</em> lacks a defined shape, presenting a constantly changing outline due to its continuous movements and body contractions. For this reason, and due to the absence of anatomical references, it has been classified as an asymmetric organism. Here, we report that a transient wound is formed in the marginal epithelium of the two new individuals produced by binary fission. By tracking the location of this epithelial wound, we can determine that successive dichotomous divisions are orthogonal to the previous division. We also found that LiCl paralyzes the cilia beating movement and body contractions and causes the placozoans to become circular in shape. This effect, as well as a stereotypic body folding behavior observed in detached placozoans and cell labeling experiments of the upper epithelium, indicate a cylindrical body symmetry for Placozoa.</p></div>","PeriodicalId":49844,"journal":{"name":"Mechanisms of Development","volume":"162 ","pages":"Article 103608"},"PeriodicalIF":2.6000,"publicationDate":"2020-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.mod.2020.103608","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mechanisms of Development","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0925477320300137","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 10

Abstract

Asexual reproduction in Trichoplax occurs mainly by binary fission and occasionally by the budding of epithelial spheres called “swarmers”. The process that leads to binary fission and the mechanisms involved in this segregation are practically unknown. Trichoplax lacks a defined shape, presenting a constantly changing outline due to its continuous movements and body contractions. For this reason, and due to the absence of anatomical references, it has been classified as an asymmetric organism. Here, we report that a transient wound is formed in the marginal epithelium of the two new individuals produced by binary fission. By tracking the location of this epithelial wound, we can determine that successive dichotomous divisions are orthogonal to the previous division. We also found that LiCl paralyzes the cilia beating movement and body contractions and causes the placozoans to become circular in shape. This effect, as well as a stereotypic body folding behavior observed in detached placozoans and cell labeling experiments of the upper epithelium, indicate a cylindrical body symmetry for Placozoa.

盘虫的二元裂变与随后的分裂平面是正交的
毛原虫的无性生殖主要通过二元分裂进行,偶尔也通过被称为“蜂群”的上皮球的出芽进行。导致二元裂变的过程和这种分离所涉及的机制实际上是未知的。毛虫缺乏明确的形状,由于其不断运动和身体收缩,呈现出不断变化的轮廓。由于这个原因,并且由于缺乏解剖学参考,它被归类为不对称生物。在这里,我们报告了在二元裂变产生的两个新个体的边缘上皮中形成的短暂伤口。通过跟踪这个上皮伤口的位置,我们可以确定连续的二分类与之前的分裂是正交的。我们还发现LiCl使纤毛跳动运动和身体收缩麻痹,并使placozoan变成圆形。这种效应,以及在离体盘虫和上上皮细胞标记实验中观察到的刻板的身体折叠行为,表明盘虫的身体呈圆柱形对称。
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
Mechanisms of Development
Mechanisms of Development 生物-发育生物学
CiteScore
3.60
自引率
0.00%
发文量
0
审稿时长
12.4 weeks
期刊介绍: Mechanisms of Development is an international journal covering the areas of cell biology and developmental biology. In addition to publishing work at the interphase of these two disciplines, we also publish work that is purely cell biology as well as classical developmental biology. Mechanisms of Development will consider papers in any area of cell biology or developmental biology, in any model system like animals and plants, using a variety of approaches, such as cellular, biomechanical, molecular, quantitative, computational and theoretical biology. Areas of particular interest include: Cell and tissue morphogenesis Cell adhesion and migration Cell shape and polarity Biomechanics Theoretical modelling of cell and developmental biology Quantitative biology Stem cell biology Cell differentiation Cell proliferation and cell death Evo-Devo Membrane traffic Metabolic regulation Organ and organoid development Regeneration Mechanisms of Development does not publish descriptive studies of gene expression patterns and molecular screens; for submission of such studies see Gene Expression Patterns.
×
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