The sclerotome is the source of the dorsal and anal fin skeleton and its expansion is required for median fin development.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2024-11-22 DOI:10.1242/dev.203025
Raisa Bailon-Zambrano, Margaret K Keating, Emily C Sales, Abigail R Nichols, Grace E Gustafson, Colette A Hopkins, Katrinka M Kocha, Peng Huang, Lindsey Barske, James T Nichols
{"title":"The sclerotome is the source of the dorsal and anal fin skeleton and its expansion is required for median fin development.","authors":"Raisa Bailon-Zambrano, Margaret K Keating, Emily C Sales, Abigail R Nichols, Grace E Gustafson, Colette A Hopkins, Katrinka M Kocha, Peng Huang, Lindsey Barske, James T Nichols","doi":"10.1242/dev.203025","DOIUrl":null,"url":null,"abstract":"<p><p>Paired locomotion appendages are hypothesized to have redeployed the developmental program of median appendages, such as the dorsal and anal fins. Compared with paired fins, and limbs, median appendages remain surprisingly understudied. Here, we report that a dominant zebrafish mutant, smoothback(smb), fails to develop a dorsal fin. Moreover, the anal fin is reduced along the antero-posterior axis, and spine defects develop. Mechanistically, smb is caused by an insertion of a sox10:Gal4VP16transgenic construct into a non-coding region. The first step in fin, and limb, induction is aggregation of undifferentiated mesenchyme at the appendage development site. In smb, this dorsal fin mesenchyme is absent. Lineage tracing demonstrates the previously unknown developmental origin of the mesenchyme, the sclerotome, which also gives rise to the spine. Strikingly, we find that there is significantly less sclerotome in smb compared to wild type. Our results give insight into the origin and modularity of understudied median fins, which have changed position, number, size, and even disappeared across evolutionary time.</p>","PeriodicalId":11375,"journal":{"name":"Development","volume":" ","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Development","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1242/dev.203025","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Paired locomotion appendages are hypothesized to have redeployed the developmental program of median appendages, such as the dorsal and anal fins. Compared with paired fins, and limbs, median appendages remain surprisingly understudied. Here, we report that a dominant zebrafish mutant, smoothback(smb), fails to develop a dorsal fin. Moreover, the anal fin is reduced along the antero-posterior axis, and spine defects develop. Mechanistically, smb is caused by an insertion of a sox10:Gal4VP16transgenic construct into a non-coding region. The first step in fin, and limb, induction is aggregation of undifferentiated mesenchyme at the appendage development site. In smb, this dorsal fin mesenchyme is absent. Lineage tracing demonstrates the previously unknown developmental origin of the mesenchyme, the sclerotome, which also gives rise to the spine. Strikingly, we find that there is significantly less sclerotome in smb compared to wild type. Our results give insight into the origin and modularity of understudied median fins, which have changed position, number, size, and even disappeared across evolutionary time.

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
硬骨是背鳍和臀鳍骨骼的来源,中鳍的发育需要硬骨的扩张。
据推测,成对运动附肢重新部署了背鳍和臀鳍等中位附肢的发育程序。与成对的鳍和四肢相比,中位附肢的研究仍然不足,令人惊讶。在这里,我们报告了一种显性斑马鱼突变体--smoothback(smb)--不能发育背鳍。此外,臀鳍沿前后轴缩小,并出现脊柱缺陷。从机理上讲,smb 是由插入到非编码区的 sox10:Gal4VP16 转基因构建体引起的。鳍和肢体诱导的第一步是未分化间充质在附肢发育部位聚集。在 smb 中,这种背鳍间充质不存在。系谱追踪显示了间充质以前未知的发育起源--硬骨,这也是脊柱的起源。令人震惊的是,我们发现与野生型相比,smb 中的硬质体明显较少。我们的研究结果让我们对研究不足的中鳍的起源和模块化有了深入的了解,中鳍在进化过程中位置、数量、大小都发生了变化,甚至消失了。
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 去求助
来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
期刊最新文献
ARPP19 phosphorylation site evolution and the switch in cAMP control of oocyte maturation in vertebrates. Barcoding Notch signaling in the developing brain. Cellular retinoic acid binding proteins regulate germ cell proliferation and sex determination in zebrafish. Phospho-regulation of ASCL1-mediated chromatin opening during cellular reprogramming. Short-range Fgf signalling patterns hindbrain progenitors to induce the neurogenesis-to-oligodendrogenesis switch.
×
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