A whole-body atlas of BMP signaling activity in an adult sea anemone.

IF 4.5 1区 生物学 Q1 BIOLOGY BMC Biology Pub Date : 2025-02-21 DOI:10.1186/s12915-025-02150-w
Paul Knabl, David Mörsdorf, Grigory Genikhovich
{"title":"A whole-body atlas of BMP signaling activity in an adult sea anemone.","authors":"Paul Knabl, David Mörsdorf, Grigory Genikhovich","doi":"10.1186/s12915-025-02150-w","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>BMP signaling is responsible for the second body axis patterning in Bilateria and in the bilaterally symmetric members of the bilaterian sister clade Cnidaria-corals and sea anemones. However, medusozoan cnidarians (jellyfish, hydroids) are radially symmetric, and yet their genomes contain BMP signaling components. This evolutionary conservation suggests that BMP signaling must have other functions not related to axial patterning, which keeps BMP signaling components under selective pressure.</p><p><strong>Results: </strong>To find out what these functions might be, we generated a detailed whole-body atlas of BMP activity in the sea anemone Nematostella. In the adult polyp, we discover an unexpected diversity of domains with BMP signaling activity, which is especially prominent in the head, as well as across the neuro-muscular and reproductive parts of the gastrodermis. In accordance, analysis of two medusozoan species, the true jellyfish Aurelia and the box jellyfish Tripedalia, revealed similarly broad and diverse BMP activity.</p><p><strong>Conclusions: </strong>Our study reveals multiple, distinct domains of BMP signaling in Anthozoa and Medusozoa, supporting the versatile nature of the BMP pathway across Cnidaria. Most prominently, BMP signaling appears to be involved in tentacle formation, neuronal development, and gameto- or gonadogenesis.</p>","PeriodicalId":9339,"journal":{"name":"BMC Biology","volume":"23 1","pages":"49"},"PeriodicalIF":4.5000,"publicationDate":"2025-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11846459/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12915-025-02150-w","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: BMP signaling is responsible for the second body axis patterning in Bilateria and in the bilaterally symmetric members of the bilaterian sister clade Cnidaria-corals and sea anemones. However, medusozoan cnidarians (jellyfish, hydroids) are radially symmetric, and yet their genomes contain BMP signaling components. This evolutionary conservation suggests that BMP signaling must have other functions not related to axial patterning, which keeps BMP signaling components under selective pressure.

Results: To find out what these functions might be, we generated a detailed whole-body atlas of BMP activity in the sea anemone Nematostella. In the adult polyp, we discover an unexpected diversity of domains with BMP signaling activity, which is especially prominent in the head, as well as across the neuro-muscular and reproductive parts of the gastrodermis. In accordance, analysis of two medusozoan species, the true jellyfish Aurelia and the box jellyfish Tripedalia, revealed similarly broad and diverse BMP activity.

Conclusions: Our study reveals multiple, distinct domains of BMP signaling in Anthozoa and Medusozoa, supporting the versatile nature of the BMP pathway across Cnidaria. Most prominently, BMP signaling appears to be involved in tentacle formation, neuronal development, and gameto- or gonadogenesis.

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
成体海葵BMP信号活动的全身图谱。
背景:BMP信号在双侧门和双侧对称的姐妹分支刺胞虫-珊瑚和海葵中负责第二体轴图案。然而,水母、水螅等水母动物是径向对称的,但它们的基因组中含有BMP信号成分。这种进化守恒表明,BMP信号必须具有与轴向模式无关的其他功能,轴向模式使BMP信号成分处于选择压力下。结果:为了找出这些功能可能是什么,我们生成了海葵Nematostella BMP活性的详细全身图谱。在成年息肉中,我们发现了BMP信号活动的意想不到的多样性,这在头部以及胃真皮层的神经肌肉和生殖部分尤为突出。同样,对两种水母(真水母Aurelia和箱形水母Tripedalia)的分析也显示出同样广泛而多样的BMP活性。结论:我们的研究揭示了刺胞动物中BMP信号的多个不同域,支持BMP信号通路在刺胞动物中的多用途性。最显著的是,BMP信号似乎参与了触须形成、神经元发育和配子或性腺生成。
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
BMC Biology
BMC Biology 生物-生物学
CiteScore
7.80
自引率
1.90%
发文量
260
审稿时长
3 months
期刊介绍: BMC Biology is a broad scope journal covering all areas of biology. Our content includes research articles, new methods and tools. BMC Biology also publishes reviews, Q&A, and commentaries.
期刊最新文献
Extraordinary diversity of antiviral immune-related gene families across 38 bat species. Whole genomes reveal subpopulations and isolation-by-distance patterns in the Norwegian lemming. Modeling age-related methylation changes in vitro with intestinal organoids. The genome of the relict earless monitor lizard, Lanthanotus borneensis, and the Toxicofera hypothesis. Different modality-specific mechanisms mediate serial dependence effects in visual and auditory perception.
×
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:604180095
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