Literature DB >> 29569346

Evolution of caudal fin ray development and caudal fin hypural diastema complex in spotted gar, teleosts, and other neopterygian fishes.

Thomas Desvignes1, Andrew Carey1, John H Postlethwait1.   

Abstract

BACKGROUND: The caudal fin of actinopterygians transitioned from a heterocercal dorsoventrally asymmetrical fin to a homocercal externally symmetrical fin in teleosts through poorly understood evolutionary developmental mechanisms. We studied the caudal skeleton of major living actinopterygian lineages, including polypteriformes, acipenseriformes, Holostei (gars and bowfin), and teleosts, compared with reports of extinct neopterygians and basal teleosteans. We focused on the hypural diastema complex, which includes (1) a gap between hypurals 2 and 3, that (2) separates two plates of connective tissue at (3) the branching of caudal vasculature; these features had been considered as a shared, derived trait of teleosts, a synapomorphy.
RESULTS: These studies revealed that gars and teleosts share all three features of the hypural diastema complex. Absence of a complex with these features from bowfin, fossil Holostei, and stem Teleostei argues in favor of repetitive, independent emergence in several neopterygian and basal Teleostei lineages, or less likely, many independent losses. We further observed that, in gars and teleosts, the earliest developing lepidotrichia align with the horizontal adult body axis, thus participating in external symmetry.
CONCLUSIONS: These results suggest that the hypural diastema complex in teleosts and gars represents a homoplasy among neopterygians and that it emerged repeatedly by parallel evolution due to shared inherited underlying genetic and developmental programs (latent homology). Because the hypural diastema complex exists in gars with heterocercal tails, this complex is independent of homocercality. Developmental Dynamics 247:832-853, 2018.
© 2018 Wiley Periodicals, Inc. © 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  Amia calva; Danio rerio; Gasterosteus aculeatus; Holostei; Lepisosteus; ontogeny; plate of connective tissue; tail

Mesh:

Year:  2018        PMID: 29569346      PMCID: PMC5980753          DOI: 10.1002/dvdy.24630

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  35 in total

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5.  The Caudal Skeleton of the Zebrafish, Danio rerio, from a Phylogenetic Perspective: A Polyural Interpretation of Homologous Structures.

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7.  Skeletal development in the heterocercal caudal fin of spotted gar (lepisosteus oculatus) and other lepisosteiformes.

Authors:  Thomas Desvignes; Andrew Carey; Ingo Braasch; Trevor Enright; John H Postlethwait
Journal:  Dev Dyn       Date:  2018-01-31       Impact factor: 3.780

8.  Caudal fin shape modulation and control during acceleration, braking and backing maneuvers in bluegill sunfish, Lepomis macrochirus.

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9.  A Phylogenomic Perspective on the Radiation of Ray-Finned Fishes Based upon Targeted Sequencing of Ultraconserved Elements (UCEs).

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Journal:  PLoS Curr       Date:  2013-04-18
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1.  Coordinated patterning of zebrafish caudal fin symmetry by a central and two peripheral organizers.

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Journal:  Dev Dyn       Date:  2022-04-22       Impact factor: 2.842

2.  Skeletal development in the heterocercal caudal fin of spotted gar (lepisosteus oculatus) and other lepisosteiformes.

Authors:  Thomas Desvignes; Andrew Carey; Ingo Braasch; Trevor Enright; John H Postlethwait
Journal:  Dev Dyn       Date:  2018-01-31       Impact factor: 3.780

3.  Gene expression profiling suggests differences in molecular mechanisms of fin elongation between cichlid species.

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Review 5.  Function of Circular RNAs in Fish and Their Potential Application as Biomarkers.

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  5 in total

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