发展过程的数学建模

IF 1.7 4区 生物学 Q4 CELL BIOLOGY Development Growth & Differentiation Pub Date : 2023-05-16 DOI:10.1111/dgd.12856
Yoh Iwasa
{"title":"发展过程的数学建模","authors":"Yoh Iwasa","doi":"10.1111/dgd.12856","DOIUrl":null,"url":null,"abstract":"<p>We review several mathematical models and concepts in developmental biology that have been established over the last decade. (1) Feedback vertex set: Ascidian embryos contain cells of seven types, and cell fate is controlled by ~100 interacting genes. The “feedback vertex set” of the directed graph of the gene regulatory network consists of a small number of genes. By experimentally manipulating them, we can differentiate cells into any cell type. (2) Tissue deformation: Describing morphological changes in tissues and relating them to gene expression and other cellular processes is key in understanding morphogenesis. Expansion and anisotropy of the tissue are described by a “deformation tensor” at each location. A study on chick limb bud formation revealed that both the volume growth rate and anisotropy in deformation differed significantly between locations and stages. (3) Mechanobiology: Forces operating on each cell may alter cell shape and gene expression, which may subsequently exert forces on their surroundings. Measurements of force, tissue shape, and gene expression help us understand autonomous tissue deformation. (4) Adaptive design of development: An optimal growth schedule in fluctuating environments explains the growth response to starvation in <i>Drosophila</i> larvae. Adaptive placement of morphogen sources makes development robust to noises.</p>","PeriodicalId":50589,"journal":{"name":"Development Growth & Differentiation","volume":"65 5","pages":"272-281"},"PeriodicalIF":1.7000,"publicationDate":"2023-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/dgd.12856","citationCount":"0","resultStr":"{\"title\":\"Mathematical modeling for developmental processes\",\"authors\":\"Yoh Iwasa\",\"doi\":\"10.1111/dgd.12856\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>We review several mathematical models and concepts in developmental biology that have been established over the last decade. (1) Feedback vertex set: Ascidian embryos contain cells of seven types, and cell fate is controlled by ~100 interacting genes. The “feedback vertex set” of the directed graph of the gene regulatory network consists of a small number of genes. By experimentally manipulating them, we can differentiate cells into any cell type. (2) Tissue deformation: Describing morphological changes in tissues and relating them to gene expression and other cellular processes is key in understanding morphogenesis. Expansion and anisotropy of the tissue are described by a “deformation tensor” at each location. A study on chick limb bud formation revealed that both the volume growth rate and anisotropy in deformation differed significantly between locations and stages. (3) Mechanobiology: Forces operating on each cell may alter cell shape and gene expression, which may subsequently exert forces on their surroundings. Measurements of force, tissue shape, and gene expression help us understand autonomous tissue deformation. (4) Adaptive design of development: An optimal growth schedule in fluctuating environments explains the growth response to starvation in <i>Drosophila</i> larvae. Adaptive placement of morphogen sources makes development robust to noises.</p>\",\"PeriodicalId\":50589,\"journal\":{\"name\":\"Development Growth & Differentiation\",\"volume\":\"65 5\",\"pages\":\"272-281\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2023-05-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/dgd.12856\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Development Growth & Differentiation\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/dgd.12856\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Development Growth & Differentiation","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/dgd.12856","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

我们回顾了过去十年来在发育生物学中建立的几个数学模型和概念。(1)反馈顶点集:海鞘胚胎包含7种类型的细胞,细胞命运由约100个相互作用的基因控制。基因调控网络有向图的“反馈顶点集”由少量基因组成。通过实验操纵它们,我们可以将细胞分化成任何类型的细胞。(2)组织变形:描述组织的形态变化并将其与基因表达和其他细胞过程联系起来是理解形态发生的关键。组织的膨胀和各向异性由每个位置的“变形张量”来描述。对雏鸡肢体芽形成的研究表明,不同部位和阶段的雏鸡肢体芽的体积生长率和变形各向异性均有显著差异。(3)机械生物学:作用于每个细胞的力可能改变细胞形状和基因表达,这可能随后对其周围环境施加力。力、组织形状和基因表达的测量帮助我们理解自主组织变形。(4)发育的适应性设计:波动环境下的最佳生长计划解释了果蝇幼虫对饥饿的生长反应。形态源的自适应放置使发育对噪声具有鲁棒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

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
Mathematical modeling for developmental processes

We review several mathematical models and concepts in developmental biology that have been established over the last decade. (1) Feedback vertex set: Ascidian embryos contain cells of seven types, and cell fate is controlled by ~100 interacting genes. The “feedback vertex set” of the directed graph of the gene regulatory network consists of a small number of genes. By experimentally manipulating them, we can differentiate cells into any cell type. (2) Tissue deformation: Describing morphological changes in tissues and relating them to gene expression and other cellular processes is key in understanding morphogenesis. Expansion and anisotropy of the tissue are described by a “deformation tensor” at each location. A study on chick limb bud formation revealed that both the volume growth rate and anisotropy in deformation differed significantly between locations and stages. (3) Mechanobiology: Forces operating on each cell may alter cell shape and gene expression, which may subsequently exert forces on their surroundings. Measurements of force, tissue shape, and gene expression help us understand autonomous tissue deformation. (4) Adaptive design of development: An optimal growth schedule in fluctuating environments explains the growth response to starvation in Drosophila larvae. Adaptive placement of morphogen sources makes development robust to noises.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Development Growth & Differentiation
Development Growth & Differentiation 生物-发育生物学
CiteScore
4.60
自引率
4.00%
发文量
62
审稿时长
6 months
期刊介绍: Development Growth & Differentiation (DGD) publishes three types of articles: original, resource, and review papers. Original papers are on any subjects having a context in development, growth, and differentiation processes in animals, plants, and microorganisms, dealing with molecular, genetic, cellular and organismal phenomena including metamorphosis and regeneration, while using experimental, theoretical, and bioinformatic approaches. Papers on other related fields are also welcome, such as stem cell biology, genomics, neuroscience, Evodevo, Ecodevo, and medical science as well as related methodology (new or revised techniques) and bioresources. Resource papers describe a dataset, such as whole genome sequences and expressed sequence tags (ESTs), with some biological insights, which should be valuable for studying the subjects as mentioned above. Submission of review papers is also encouraged, especially those providing a new scope based on the authors’ own study, or a summarization of their study series.
期刊最新文献
Quantitative in toto live imaging analysis of apical nuclear migration in the mouse telencephalic neuroepithelium. Labeling and sorting of avian primordial germ cells utilizing Lycopersicon Esculentum lectin. Transition from fetal to postnatal state in the heart: Crosstalk between metabolism and regeneration. Issue Information Mitochondrial DNA replication is essential for neurogenesis but not gliogenesis in fetal neural stem cells
×
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