Affordable Access

Publisher Website

Development of the electric organ in embryos and larvae of the knifefish, Brachyhypopomus gauderio.

Authors
  • Alshami, Ilham J J1
  • Ono, Yosuke2
  • Correia, Ana3
  • Hacker, Christian1
  • Lange, Anke1
  • Scholpp, Steffen4
  • Kawasaki, Masashi5
  • Ingham, Philip W6
  • Kudoh, Tetsuhiro7
  • 1 Biosciences, College of Life and Environmental Sciences, University of Exeter, Exeter, EX4 4QD, UK.
  • 2 Biosciences, College of Life and Environmental Sciences, University of Exeter, Exeter, EX4 4QD, UK; Living Systems Institute, University of Exeter, Exeter, EX4 4QD, UK.
  • 3 Department of Physiology, Development and Neuroscience, University of Cambridge, CB2 3EG, UK.
  • 4 Living Systems Institute, University of Exeter, Exeter, EX4 4QD, UK.
  • 5 Department of Biology, University of Virginia, Charlottesville, VA, 22904, USA.
  • 6 Living Systems Institute, University of Exeter, Exeter, EX4 4QD, UK; Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore. , (Singapore)
  • 7 Biosciences, College of Life and Environmental Sciences, University of Exeter, Exeter, EX4 4QD, UK. Electronic address: [email protected].
Type
Published Article
Journal
Developmental Biology
Publisher
Elsevier
Publication Date
Oct 01, 2020
Volume
466
Issue
1-2
Pages
99–108
Identifiers
DOI: 10.1016/j.ydbio.2020.06.010
PMID: 32687892
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

South American Gymnotiform knifefish possess electric organs that generate electric fields for electro-location and electro-communication. Electric organs in fish can be derived from either myogenic cells (myogenic electric organ/mEO) or neurogenic cells (neurogenic electric organ/nEO). To date, the embryonic development of EOs has remained obscure. Here we characterize the development of the mEO in the Gymnotiform bluntnose knifefish, Brachyhypopomus gauderio. We find that EO primordial cells arise during embryonic stages in the ventral edge of the tail myotome, translocate into the ventral fin and develop into syncytial electrocytes at early larval stages. We also describe a pair of thick nerve cords that flank the dorsal aorta, the location and characteristic morphology of which are reminiscent of the nEO in Apteronotid species, suggesting a common evolutionary origin of these tissues. Taken together, our findings reveal the embryonic origins of the mEO and provide a basis for elucidating the mechanisms of evolutionary diversification of electric charge generation by myogenic and neurogenic EOs. Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

Report this publication

Statistics

Seen <100 times