• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

两侧对称动物平滑肌细胞和横纹肌细胞的进化起源。

The evolutionary origin of bilaterian smooth and striated myocytes.

作者信息

Brunet Thibaut, Fischer Antje Hl, Steinmetz Patrick Rh, Lauri Antonella, Bertucci Paola, Arendt Detlev

机构信息

Developmental Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany.

出版信息

Elife. 2016 Dec 1;5:e19607. doi: 10.7554/eLife.19607.

DOI:10.7554/eLife.19607
PMID:27906129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5167519/
Abstract

The dichotomy between smooth and striated myocytes is fundamental for bilaterian musculature, but its evolutionary origin is unsolved. In particular, interrelationships of visceral smooth muscles remain unclear. Absent in fly and nematode, they have not yet been characterized molecularly outside vertebrates. Here, we characterize expression profile, ultrastructure, contractility and innervation of the musculature in the marine annelid and identify smooth muscles around the midgut, hindgut and heart that resemble their vertebrate counterparts in molecular fingerprint, contraction speed and nervous control. Our data suggest that both visceral smooth and somatic striated myocytes were present in the protostome-deuterostome ancestor and that smooth myocytes later co-opted the striated contractile module repeatedly - for example, in vertebrate heart evolution. During these smooth-to-striated myocyte conversions, the core regulatory complex of transcription factors conveying myocyte identity remained unchanged, reflecting a general principle in cell type evolution.

摘要

平滑肌细胞和横纹肌细胞之间的二分法是两侧对称动物肌肉组织的基础,但其进化起源尚未解决。特别是,内脏平滑肌之间的相互关系仍不清楚。果蝇和线虫中没有内脏平滑肌,在脊椎动物之外它们尚未在分子层面得到表征。在这里,我们描述了海洋环节动物肌肉组织的表达谱、超微结构、收缩性和神经支配,并识别出中肠、后肠和心脏周围的平滑肌,这些平滑肌在分子指纹、收缩速度和神经控制方面与它们的脊椎动物对应物相似。我们的数据表明,内脏平滑肌细胞和体壁横纹肌细胞在原口动物 - 后口动物的祖先中就已存在,并且平滑肌细胞后来多次采用了横纹肌收缩模块——例如,在脊椎动物心脏进化过程中。在这些从平滑肌细胞到横纹肌细胞的转变过程中,传达肌细胞身份的转录因子的核心调节复合体保持不变,这反映了细胞类型进化中的一个普遍原则。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/31ee9356120c/elife-19607-fig7-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/c468467fee17/elife-19607-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/48b75103bb48/elife-19607-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/67bc77b08c69/elife-19607-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/8bcd37aad7a7/elife-19607-fig2-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/a4620639df0f/elife-19607-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/fcbf255e86d5/elife-19607-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/a908bd643ed3/elife-19607-fig3-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/40fafefb7d32/elife-19607-fig3-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/4515ed53a9bf/elife-19607-fig3-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/5b007ea7d665/elife-19607-fig3-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/76e83840b581/elife-19607-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/32a704af5994/elife-19607-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/e20978152d9a/elife-19607-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/8e19edc39f0b/elife-19607-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/3403f9a71d52/elife-19607-fig7-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/8a9db40f9d8b/elife-19607-fig7-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/31ee9356120c/elife-19607-fig7-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/c468467fee17/elife-19607-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/48b75103bb48/elife-19607-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/67bc77b08c69/elife-19607-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/8bcd37aad7a7/elife-19607-fig2-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/a4620639df0f/elife-19607-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/fcbf255e86d5/elife-19607-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/a908bd643ed3/elife-19607-fig3-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/40fafefb7d32/elife-19607-fig3-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/4515ed53a9bf/elife-19607-fig3-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/5b007ea7d665/elife-19607-fig3-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/76e83840b581/elife-19607-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/32a704af5994/elife-19607-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/e20978152d9a/elife-19607-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/8e19edc39f0b/elife-19607-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/3403f9a71d52/elife-19607-fig7-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/8a9db40f9d8b/elife-19607-fig7-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e17e/5167519/31ee9356120c/elife-19607-fig7-figsupp3.jpg

相似文献

1
The evolutionary origin of bilaterian smooth and striated myocytes.两侧对称动物平滑肌细胞和横纹肌细胞的进化起源。
Elife. 2016 Dec 1;5:e19607. doi: 10.7554/eLife.19607.
2
Whole-organism cellular gene-expression atlas reveals conserved cell types in the ventral nerve cord of .全器官细胞基因表达图谱揭示了 腹神经索中保守的细胞类型。
Proc Natl Acad Sci U S A. 2017 Jun 6;114(23):5878-5885. doi: 10.1073/pnas.1610602114.
3
Did the notochord evolve from an ancient axial muscle? The axochord hypothesis.脊索是从古老的轴肌进化而来的吗?轴索假说。
Bioessays. 2015 Aug;37(8):836-50. doi: 10.1002/bies.201500027. Epub 2015 Jul 14.
4
DNA methylation atlas and machinery in the developing and regenerating annelid Platynereis dumerilii.在发育和再生环节动物扁形虫 Platynereis dumerilii 中的 DNA 甲基化图谱和机制。
BMC Biol. 2021 Aug 3;19(1):148. doi: 10.1186/s12915-021-01074-5.
5
Linking micro- and macro-evolution at the cell type level: a view from the lophotrochozoan Platynereis dumerilii.在细胞类型水平上连接微观进化和宏观进化:来自担轮动物 Platynereis dumerilii 的观点。
Brief Funct Genomics. 2013 Sep;12(5):430-9. doi: 10.1093/bfgp/els049. Epub 2012 Nov 20.
6
Development of the annelid axochord: insights into notochord evolution.环节动物脊索的发育:对脊索进化的深入了解。
Science. 2014 Sep 12;345(6202):1365-8. doi: 10.1126/science.1253396.
7
Independent evolution of striated muscles in cnidarians and bilaterians.刺胞动物和两侧对称动物横纹肌的独立进化。
Nature. 2012 Jul 12;487(7406):231-4. doi: 10.1038/nature11180.
8
PdumBase: a transcriptome database and research tool for Platynereis dumerilii and early development of other metazoans.PdumBase:一种用于皮氏狼牙虾虎鱼和其他后生动物早期发育的转录组数据库和研究工具。
BMC Genomics. 2018 Aug 16;19(1):618. doi: 10.1186/s12864-018-4987-0.
9
Ancient animal microRNAs and the evolution of tissue identity.远古动物 microRNAs 与组织特性的演化
Nature. 2010 Feb 25;463(7284):1084-8. doi: 10.1038/nature08744. Epub 2010 Jan 31.
10
Characterization of several invertebrate muscle cell types: a comparison with vertebrate muscles.几种无脊椎动物肌肉细胞类型的特征:与脊椎动物肌肉的比较。
Microsc Res Tech. 2000 Jan 15;48(2):107-15. doi: 10.1002/(SICI)1097-0029(20000115)48:2<107::AID-JEMT6>3.0.CO;2-U.

引用本文的文献

1
Whole-body connectome of a segmented annelid larva.分段环节动物幼虫的全身连接组
Elife. 2025 Aug 27;13:RP97964. doi: 10.7554/eLife.97964.
2
Cell type and cell signalling innovations underlying mammalian pregnancy.哺乳动物妊娠背后的细胞类型和细胞信号转导创新。
Nat Ecol Evol. 2025 Jul 1. doi: 10.1038/s41559-025-02748-x.
3
The Ancestor and Evolution of the Giant Muscle Protein Connectin/Titin.巨型肌肉蛋白连接蛋白/肌联蛋白的起源与进化

本文引用的文献

1
The origin and evolution of cell types.细胞类型的起源与演化。
Nat Rev Genet. 2016 Dec;17(12):744-757. doi: 10.1038/nrg.2016.127. Epub 2016 Nov 7.
2
Animal Evolution: The Hard Problem of Cartilage Origins.动物进化:软骨起源的难题
Curr Biol. 2016 Jul 25;26(14):R685-8. doi: 10.1016/j.cub.2016.05.062.
3
Coregulation of tandem duplicate genes slows evolution of subfunctionalization in mammals.串联重复基因的共同调控减缓了哺乳动物亚功能化的进化。
J Mol Evol. 2025 Apr 27. doi: 10.1007/s00239-025-10247-7.
4
Molecular profiles, sources and lineage restrictions of stem cells in an annelid regeneration model.环节动物再生模型中干细胞的分子特征、来源和谱系限制。
Nat Commun. 2024 Nov 18;15(1):9882. doi: 10.1038/s41467-024-54041-3.
5
Tissue specificity follows gene duplication.组织特异性遵循基因复制。
Nat Ecol Evol. 2024 Jun;8(6):1068-1069. doi: 10.1038/s41559-024-02394-9.
6
Stem cell proliferation and differentiation during larval metamorphosis of the model tapeworm .在模式扁形虫幼虫变态过程中干细胞的增殖和分化。
Front Cell Infect Microbiol. 2023 Oct 16;13:1286190. doi: 10.3389/fcimb.2023.1286190. eCollection 2023.
7
Stepwise emergence of the neuronal gene expression program in early animal evolution.早期动物进化中神经元基因表达程序的逐步出现。
Cell. 2023 Oct 12;186(21):4676-4693.e29. doi: 10.1016/j.cell.2023.08.027. Epub 2023 Sep 19.
8
New hypotheses of cell type diversity and novelty from orthology-driven comparative single cell and nuclei transcriptomics in echinoderms.从棘皮动物的直系同源物驱动的比较单细胞和细胞核转录组学中获得细胞类型多样性和新颖性的新假设。
Elife. 2023 Jul 20;12:e80090. doi: 10.7554/eLife.80090.
9
Muscle cell-type diversification is driven by bHLH transcription factor expansion and extensive effector gene duplications.肌细胞类型多样化是由 bHLH 转录因子的扩展和广泛的效应基因重复驱动的。
Nat Commun. 2023 Mar 29;14(1):1747. doi: 10.1038/s41467-023-37220-6.
10
Remodeling of the Musculature during Sexual Maturation.性成熟过程中肌肉组织的重塑
Biology (Basel). 2023 Feb 6;12(2):254. doi: 10.3390/biology12020254.
Science. 2016 May 20;352(6288):1009-13. doi: 10.1126/science.aad8411.
4
The genetic program for cartilage development has deep homology within Bilateria.软骨发育的遗传程序在两侧对称动物中具有很深的同源性。
Nature. 2016 May 5;533(7601):86-9. doi: 10.1038/nature17398. Epub 2016 Apr 25.
5
Terminal Selectors of Neuronal Identity.神经元身份的终末选择因子
Curr Top Dev Biol. 2016;116:455-75. doi: 10.1016/bs.ctdb.2015.12.007. Epub 2016 Jan 14.
6
Xenacoelomorpha is the sister group to Nephrozoa.扁形动物门是肾形动物门的姐妹群。
Nature. 2016 Feb 4;530(7588):89-93. doi: 10.1038/nature16520.
7
From damage response to action potentials: early evolution of neural and contractile modules in stem eukaryotes.从损伤反应到动作电位:真核生物干细胞中神经和收缩模块的早期进化
Philos Trans R Soc Lond B Biol Sci. 2016 Jan 5;371(1685):20150043. doi: 10.1098/rstb.2015.0043.
8
An invertebrate smooth muscle with striated muscle myosin filaments.一种具有横纹肌肌球蛋白丝的无脊椎动物平滑肌。
Proc Natl Acad Sci U S A. 2015 Oct 20;112(42):E5660-8. doi: 10.1073/pnas.1513439112. Epub 2015 Oct 6.
9
A Cranial Mesoderm Origin for Esophagus Striated Muscles.颅中胚层起源于食管横纹肌。
Dev Cell. 2015 Sep 28;34(6):694-704. doi: 10.1016/j.devcel.2015.07.003. Epub 2015 Sep 17.
10
Character trees from transcriptome data: Origin and individuation of morphological characters and the so-called "species signal".转录组数据的特征树:形态特征的起源与个体化以及所谓的“物种信号”
J Exp Zool B Mol Dev Evol. 2015 Nov;324(7):588-604. doi: 10.1002/jez.b.22636. Epub 2015 Jul 14.