Evidence map›Paper›PMID 25696823›Full record

ReviewThe Journal of experimental biology2015

Convergent evolution of neural systems in ctenophores.

Leonid L Moroz

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of experimental biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 1 pooled it
25.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

72 citing papers in PubMed, 1 synthesis or guideline pooled it, 136 citations in OpenAlex.

  1. Pooled it
  2. Developing broad brains: the importance of an early introduction to evolutionary thinking in undergraduate neuroscience programs.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Early transitions in the evolution of cognition.History and philosophy of the life sciences · 2025
    Article
  8. Article
  9. Review
  10. Neuropeptides: The Evergreen Jack-of-All-Trades in Neuronal Circuit Development and Regulation.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  11. Article
  12. Review
  13. Making Neurobots and Chimerical Ctenophores.bioRxiv : the preprint server for biology · 2024
    Article
  14. Article
  15. Scanning Electron Microscopy of Ctenophores: Illustrative Atlas.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  16. Ctenophora: Illustrated Guide and Taxonomy.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  17. Frontiers in neuroinformatics · 2024
    Article
  18. Review
  19. Brief History of Ctenophora.Methods in molecular biology (Clifton, N.J.) · 2024
    Review
  20. Article

12 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Leonid L MorozThe Whitney Laboratory of Marine Biosciences and Department of Neuroscience and McKnight Brain Institute, University of Florida, FL 32080, USA. The Whitney Laboratory, University of Florida, 9505 Ocean Shore Boulevard, St. Augustine, FL 32080, USA moroz@whitney.ufl.edu.
Whitney Museum of American Art · US

Funding

Genomic Approaches to Deciphering Memory CircuitsR01MH097062 · NIMH · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI JU, JINGYUE, KANDEL, ERIC R · 2012 to 2016
$2.0M
Genomic Bases of Behavioral Learning: Single Cell ApproachesR01GM097502 · NIGMS · UNIVERSITY OF FLORIDA · PI HAWKINS, ROBERT D, MOROZ, LEONID L · 2011 to 2014
$1.6M
Genomic Dissection of Circuit DynamicsR21RR025699 · NCRR · UNIVERSITY OF FLORIDA · PI BUCHER, DIRK MARTIN, MOROZ, LEONID L · 2009 to 2010
$408k
Spatial Organization of the Genome in Identified Neurons of Memory CircuitsR21DA030118 · NIDA · UNIVERSITY OF FLORIDA · PI MOROZ, LEONID L · 2010 to 2011
$350k
NCRR NIH HHS R21 RR025699NCRR NIH HHS R21RR025699NIDA NIH HHS 5R21DA030118NIDA NIH HHS R21 DA030118NIGMS NIH HHS 1R01GM097502NIGMS NIH HHS R01 GM097502NIMH NIH HHS R01 MH097062NIMH NIH HHS R01MH097062
6 · The paper itself

Abstract

Neurons are defined as polarized secretory cells specializing in directional propagation of electrical signals leading to the release of extracellular messengers - features that enable them to transmit information, primarily chemical in nature, beyond their immediate neighbors without affecting all intervening cells en route. Multiple origins of neurons and synapses from different classes of ancestral secretory cells might have occurred more than once during ~600 million years of animal evolution with independent events of nervous system centralization from a common bilaterian/cnidarian ancestor without the bona fide central nervous system. Ctenophores, or comb jellies, represent an example of extensive parallel evolution in neural systems. First, recent genome analyses place ctenophores as a sister group to other animals. Second, ctenophores have a smaller complement of pan-animal genes controlling canonical neurogenic, synaptic, muscle and immune systems, and developmental pathways than most other metazoans. However, comb jellies are carnivorous marine animals with a complex neuromuscular organization and sophisticated patterns of behavior. To sustain these functions, they have evolved a number of unique molecular innovations supporting the hypothesis of massive homoplasies in the organization of integrative and locomotory systems. Third, many bilaterian/cnidarian neuron-specific genes and 'classical' neurotransmitter pathways are either absent or, if present, not expressed in ctenophore neurons (e.g. the bilaterian/cnidarian neurotransmitter, γ-amino butyric acid or GABA, is localized in muscles and presumed bilaterian neuron-specific RNA-binding protein Elav is found in non-neuronal cells). Finally, metabolomic and pharmacological data failed to detect either the presence or any physiological action of serotonin, dopamine, noradrenaline, adrenaline, octopamine, acetylcholine or histamine - consistent with the hypothesis that ctenophore neural systems evolved independently from those in other animals. Glutamate and a diverse range of secretory peptides are first candidates for ctenophore neurotransmitters. Nevertheless, it is expected that other classes of signal and neurogenic molecules would be discovered in ctenophores as the next step to decipher one of the most distinct types of neural organization in the animal kingdom.

Indexed as

Biological EvolutionAnimalsCtenophoraGenomeMusclesNervous SystemNeuronsNeurotransmitter AgentsPhylogenyNeurotransmitter AgentsCtenophoraEvolutionGenomeMnemiopsisNeuronsNeurotransmittersPhylogenyPleurobrachia

Identifiers

PMID25696823
PMCPMC4334147
OpenAlexW2108217295

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.