Towards 3D in silico modeling of the sea urchin embryonic development.

Barbara Rizzi, Nadine Peyrieras
{"title":"Towards 3D in silico modeling of the sea urchin embryonic development.","authors":"Barbara Rizzi, Nadine Peyrieras","doi":"10.1007/s12154-013-0101-x","DOIUrl":null,"url":null,"abstract":"<p><p>Embryogenesis is a dynamic process with an intrinsic variability whose understanding requires the integration of molecular, genetic, and cellular dynamics. Biological circuits function over time at the level of single cells and require a precise analysis of the topology, temporality, and probability of events. Integrative developmental biology is currently looking for the appropriate strategies to capture the intrinsic properties of biological systems. The \"-omic\" approaches require disruption of the function of the biological circuit; they provide static information, with low temporal resolution and usually with population averaging that masks fast or variable features at the cellular scale and in a single individual. This data should be correlated with cell behavior as cells are the integrators of biological activity. Cellular dynamics are captured by the in vivo microscopy observation of live organisms. This can be used to reconstruct the 3D + time cell lineage tree to serve as the basis for modeling the organism's multiscale dynamics. We discuss here the progress that has been made in this direction, starting with the reconstruction over time of three-dimensional digital embryos from in toto time-lapse imaging. Digital specimens provide the means for a quantitative description of the development of model organisms that can be stored, shared, and compared. They open the way to in silico experimentation and to a more theoretical approach to biological processes. We show, with some unpublished results, how the proposed methodology can be applied to sea urchin species that have been model organisms in the field of classical embryology and modern developmental biology for over a century. </p>","PeriodicalId":15296,"journal":{"name":"Journal of Chemical Biology","volume":"7 1","pages":"17-28"},"PeriodicalIF":0.0000,"publicationDate":"2013-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s12154-013-0101-x","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s12154-013-0101-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10

Abstract

Embryogenesis is a dynamic process with an intrinsic variability whose understanding requires the integration of molecular, genetic, and cellular dynamics. Biological circuits function over time at the level of single cells and require a precise analysis of the topology, temporality, and probability of events. Integrative developmental biology is currently looking for the appropriate strategies to capture the intrinsic properties of biological systems. The "-omic" approaches require disruption of the function of the biological circuit; they provide static information, with low temporal resolution and usually with population averaging that masks fast or variable features at the cellular scale and in a single individual. This data should be correlated with cell behavior as cells are the integrators of biological activity. Cellular dynamics are captured by the in vivo microscopy observation of live organisms. This can be used to reconstruct the 3D + time cell lineage tree to serve as the basis for modeling the organism's multiscale dynamics. We discuss here the progress that has been made in this direction, starting with the reconstruction over time of three-dimensional digital embryos from in toto time-lapse imaging. Digital specimens provide the means for a quantitative description of the development of model organisms that can be stored, shared, and compared. They open the way to in silico experimentation and to a more theoretical approach to biological processes. We show, with some unpublished results, how the proposed methodology can be applied to sea urchin species that have been model organisms in the field of classical embryology and modern developmental biology for over a century.

Abstract Image

Abstract Image

Abstract Image

海胆胚胎发育的三维计算机模拟。
胚胎发生是一个具有内在可变性的动态过程,其理解需要整合分子、遗传和细胞动力学。随着时间的推移,生物回路在单个细胞的水平上发挥作用,需要对拓扑结构、时间性和事件概率进行精确分析。综合发育生物学目前正在寻找适当的策略来捕捉生物系统的内在特性。“- omics”方法需要破坏生物回路的功能;它们提供静态信息,具有较低的时间分辨率,通常是种群平均,掩盖了细胞尺度和单个个体的快速或可变特征。这些数据应该与细胞行为相关联,因为细胞是生物活性的整合者。细胞动力学是通过活体显微观察捕获的。这可以用来重建3D +时间细胞谱系树,作为建模生物体的多尺度动力学的基础。我们在这里讨论了在这个方向上取得的进展,从三维数字胚胎的重建开始,从完全到延时成像。数字标本为可以存储、共享和比较的模式生物的发展提供了定量描述的手段。它们为计算机实验和对生物过程的更理论化的研究开辟了道路。我们展示了一些未发表的结果,如何将所提出的方法应用于海胆物种,这些物种在一个多世纪以来一直是经典胚胎学和现代发育生物学领域的模式生物。
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