Skip to content
DraconiticResearch
Search Sources API
203,234 studies31 sourcesUpdated 15 min ago
Peer-reviewedCC BY 4.0Development, Growth & Differentiation

Evidence for a Role of Hox2 in Atrial Siphon Fusion of the Ascidian Ciona

4 affiliations
  1. 1Shimoda Marine Research Center University of Tsukuba Shimoda, Shizuoka Japan
  2. 2Information Biology Laboratory, Division of Bioengineering and Bioinformatics, Faculty of Information Science and Technology Hokkaido University Sapporo Japan
  3. 3Graduate School of Agriculture, Kyoto University Kyoto Japan
  4. 4Department of Mathematical and Life Sciences Graduate School of Science, Hiroshima University Hiroshima Japan

Abstract

The hallmark of sessile adult ascidians is a vase‐like shape with a single oral and atrial siphon. Ciona, however, develops two atrial siphons after metamorphosis, which subsequently fuse into one. The mechanisms underlying this fusion are unknown. This study suggests that Hox2 controls this process. Hox2‐knockout animals using Transcription‐Activator‐Like Effector Nuclease (TALEN) retain two atrial siphons throughout their lives. During normal fusion, epidermal cells between the siphons narrow along the anterior–posterior axis. This cellular narrowing does not occur in Hox2‐knockout animals, suggesting that the shape change in the epidermal cells produces tension, allowing the atrial siphon openings to converge at the midline for fusion. Hox2‐knockout animals lack cupular organs, which are suspected hydrodynamic sensors in the internal epithelium of the fused atrial siphon and on the sperm duct. Among several knockout attempts, atrial siphon fusion was reproduced by only one TALEN pair, suggesting that this phenotype is driven by a mutation having a broader effect than those abolishing protein function. Many ascidians, unlike Ciona, develop a single atrial siphon shortly after metamorphosis. Our findings suggest that a phylogenetically conserved gene, Hox2, establishes this group‐specific atrial siphon formation mechanism in Ciona.

Related

  1. Circulating MicroRNAs as Molecular Biomarkers of Atrial Fibrillation Recurrence After Catheter Ablation: A Systematic Review and Candidate-Centered Evidence Map
    Antônio da Silva Menezes, Arthur de Sousa Silva, Alcir Júnior de Paula Nunes Meneses +2
    BiomoleculesPeer-reviewedCC BY 4.0General biochemistryCrossref
  2. Backbone and side-chain NMR resonance assignments of Ciona intestinalis\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}β γ\end{document}-crystallin
    Matthew D. Jimenez, Mina Mozafari, Cat Tuong Nguyen Hoang +3
    Biomolecular Nmr AssignmentsPeer-reviewedCC BY 4.0Full textMolecular biology & gene regulationPMC
  3. Incidental Atrial Amyloid on Surgical Pathology Revealing Transthyretin Cardiac Amyloidosis
    Jonathan Wright, Fadi Haroun, Adam Potter +3
    JACC Case ReportsPeer-reviewedCC BY-NC-ND 4.0Full textMolecular biology & gene regulationPMCDOAJ
  4. Reduced bi-atrial reservoir strain in patients with cardiac amyloidosis: a cardiac magnetic resonance feature-tracking study
    Ryosuke Kato, Hidehiro Iwakawa, Hirokazu Yoshida +5
    International Journal of Cardiology: Heart & VasculaturePeer-reviewedCC BY-NC-NDFull textMolecular biology & gene regulationDOAJEurope PMCPMC
  5. FUSION PORE CLOSURE DETERMINES SUBQUANTAL KISS-AND-RUN SEROTONIN RELEASE FROM FULLY LOADED DENSE-CORE VESICLES
    F. F. De-Miguel
    bioRxivPreprintAll rights reservedFull textBiophysicsbioRxiv
BibTeX
@article{liu2026evidence,
  title = {{Evidence for a Role of Hox2 in Atrial Siphon Fusion of the Ascidian Ciona}},
  author = {Yurong Liu and Keita Yoshida and Akiko Hozumi and Kosuke Itagaki and Nicholas Treen and Tetsushi Sakuma and Takashi Yamamoto and Toshinori Endo and Yasunori Sasakura},
  journal = {Development, Growth \& Differentiation},
  year = {2026},
  month = oct,
  doi = {10.1111/dgd.70073},
  url = {https://doi.org/10.1111/dgd.70073},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Evidence for a Role of Hox2 in Atrial Siphon Fusion of the Ascidian Ciona
AU  - Yurong Liu
AU  - Keita Yoshida
AU  - Akiko Hozumi
AU  - Kosuke Itagaki
AU  - Nicholas Treen
AU  - Tetsushi Sakuma
AU  - Takashi Yamamoto
AU  - Toshinori Endo
AU  - Yasunori Sasakura
PY  - 2026
DA  - 2026/10/01
JO  - Development, Growth & Differentiation
DO  - 10.1111/dgd.70073
UR  - https://doi.org/10.1111/dgd.70073
AB  - The hallmark of sessile adult ascidians is a vase‐like shape with a single oral and atrial siphon. Ciona, however, develops two atrial siphons after metamorphosis, which subsequently fuse into one. The mechanisms underlying this fusion are unknown. This study suggests that Hox2 controls this process. Hox2‐knockout animals using Transcription‐Activator‐Like Effector Nuclease (TALEN) retain two atrial siphons throughout their lives. During normal fusion, epidermal cells between the siphons narrow along the anterior–posterior axis. This cellular narrowing does not occur in Hox2‐knockout animals, suggesting that the shape change in the epidermal cells produces tension, allowing the atrial siphon openings to converge at the midline for fusion. Hox2‐knockout animals lack cupular organs, which are suspected hydrodynamic sensors in the internal epithelium of the fused atrial siphon and on the sperm duct. Among several knockout attempts, atrial siphon fusion was reproduced by only one TALEN pair, suggesting that this phenotype is driven by a mutation having a broader effect than those abolishing protein function. Many ascidians, unlike Ciona, develop a single atrial siphon shortly after metamorphosis. Our findings suggest that a phylogenetically conserved gene, Hox2, establishes this group‐specific atrial siphon formation mechanism in Ciona.
SN  - 0012-1592
SN  - 1440-169X
ER  -