Organization of the gymnotiform fish pallium in relation to learning and memory: IV. Expression of conserved transcription factors and implications for the evolution of dorsal telencephalon
Abstract
We have cloned the apteronotid homologs of FoxP2, Otx1, and FoxO3. There was, in the case of all three genes, good similarity between the apteronotid and human amino acid sequences: FoxP2, 78%; Otx1, 54%; FoxO3, 71%. The functional domains of these genes were conserved to a far greater extent, on average: FoxP2, 89%; Otx1, 76%; FoxO3, 82%. This led us to hypothesize that the cellular functions of these genes might also be conserved. We used in situ hybridization to examine the distribution of the mRNA transcripts of these genes in the apteronotid telencephalon. We confined our analysis to the pallial regions previously associated with learning about social signals, whose circuitry has been closely examined in the other articles of this series. We found that AptFoxP2 and AptOtx1 transcripts were expressed predominantly in the dorsocentral division of the pallium (DC); the dorsolateral division of the pallium (DL) contained only weakly labeled neurons. In both cases, the distribution of labeled neurons was very heterogeneous, and unlabeled neurons could be found adjacent to strongly labeled ones. In contrast, we found that most neurons in DL strongly expressed AptFoxO3 mRNA, although there was only weak expression in a small number of cells within DC. We briefly discuss the relevance of our results regarding the functional roles of AptFoxP2/AptOtx1‐expressing neurons in DC for communication vs. foraging behavior. We extensively discuss the implications of our results for possible homologies between DL and DC and medial and dorsal pallium of tetrapods, respectively. J. Comp. Neurol. 520:3395–3413, 2012. © 2012 Wiley Periodicals, Inc.
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The presumed homologue of the hippocampus in teleost fish shares a comparable topological position within the pallium and a number of developmental, neuroanatomical, connectivity, and histochemical similarities with the hippocampus.
“The presumed homologue of the hippocampus in teleost fish shares not only a comparable topological position within the pallium, but also a number of developmental, neuroanatomical, connectivity, and histochemical similarities.”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [175]
The teleost fish hippocampus homologue is profusely interconnected with primary and association sensory pallial areas, from which it receives highly processed sensory information required to construct map-like spatial memories and for allocentric navigation.
“Finally, like the hippocampus of mammals and other tetrapods, the teleost fish hippocampus homologue is profusely interconnected with these primary and association sensory pallial areas [164,175,199] from which it seems to receive highly processed sensory information required to construct map-like spatial memories and for allocentric navigation [175,183].”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [175]
Cites
Teleostean and mammalian forebrains contrasted: Evidence from genes to behavior
Wullimann, M. F., & Mueller, T. (2004) · Journal of Comparative Neurology · doi:10.1002/cne.20183 · Cited by 491 · see citing works
Genomic anatomy of the hippocampus
Thompson, C. L., Pathak, S. D., Jeromin, A., Ng, L. L., MacPherson, C. R., Mortrud, M. T., Cusick, A., Riley, Z. L., Sunkin, S. M., Bernard, A., et al. (2008) · Neuron · doi:10.1016/j.neuron.2008.12.008 · Cited by 403 · see citing works
Conservation of Spatial Memory Function in the Pallial Forebrain of Reptiles and Ray-Finned Fishes
Rodrı́guez, F., López, J. C., Vargas, J. P., Gómez, Y., Broglio, C., & Salas, C. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-07-02894.2002 · Cited by 316 · see citing works
The Forebrain of Gnathostomes: In Search of a Morphotype; pp. 275–288
Northcutt, R. G. (2008) · Brain, Behavior and Evolution · doi:10.1159/000113279 · Cited by 233 · see citing works
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Fotowat, H., Lee, C., Jun, J. J., & Maler, L. (2019) · eLife · doi:10.7554/elife.44119 · Cited by 69 · see citing works
Self-citationSpatial Cognition in Teleost Fish: Strategies and Mechanisms
Rodríguez, F., Quintero, B., Amores, L., Madrid, D., Salas-Peña, C., & Salas, C. (2021) · Animals · doi:10.3390/ani11082271 · Cited by 59 · see citing works
- Authors
- Harvey‐Girard, E., Giassi, A. C. C., Ellis, W., & Maler, L.
- Affiliations
- University of Ottawa (CA)
- Corresponding author
- Harvey‐Girard, Erik
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 2012-08-16
- Volume
- 520
- Issue
- 15
- Pages
- 3395-3413
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W1975928668
- Cited by
- 54
- References
- 4
- Citations by year
- 2025: 1 · 2024: 1 · 2023: 1 · 2022: 4 · 2021: 8 · 2020: 1 · 2019: 7 · 2018: 3 · 2017: 7 · 2016: 4 · 2015: 5 · 2014: 5 · 2013: 3 · 2012: 4
- FWCI
- 2.18
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Canadian Institutes of Health Research (57084)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Physical Sciences › Environmental Science › Nature and Landscape Conservation › Fish biology, ecology, and behavior
- Keywords
- FOXP2, Otx1, FOXO3, transcription factors, social learning, memory
- MeSH terms
- Forkhead Box Protein O3, Animals, Behavior, Animal, Female, Learning, Male, Memory, Neurons, Phylogeny, RNA, Messenger, Telencephalon, Transcription Factors, Antisense Elements (Genetics), Conserved Sequence, Sequence Homology, Amino Acid, Evolution, Molecular, Gymnotiformes, Xenopus Proteins, Zebrafish Proteins, Otx Transcription Factors, Forkhead Transcription Factors
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