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  TMT-Opsins differentially modulate medaka brain function in a context-dependent manner

Fontinha, B. M., Zekoll, T., Al-Rawi, M., Gallach, M., Reithofer, F., Barker, A. J., et al. (2021). TMT-Opsins differentially modulate medaka brain function in a context-dependent manner. PLoS Biol., 19(1): e3001012. doi:10.1371/journal.pbio.3001012.

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Fontinha, Bruno M.1, Author
Zekoll, Theresa 1, Author
Al-Rawi, Mariam 1, Author
Gallach , Miguel 2, Author
Reithofer, Florian 1, Author
Barker, Alison J.3, Author           
Hofbauer, Maximilian1, Author
Fischer, Ruth M. 1, Author
von Haeseler, Arndt 1, Author
Baier, Herwig4, Author           
Tessmar-Raible, Kristin 1, Author
Affiliations:
1Max F. Perutz Laboratories, University of Vienna, Vienna, Austria, Research Platform ‘‘Rhythms of Life,” University of Vienna, , Vienna, Austria, ou_persistent22              
2Center for Integrative Bioinformatics Vienna, Max F. Perutz Laboratories, University of Vienna and Medical University of Vienna,, Vienna, Austria , ou_persistent22              
3Social Systems and Circuits Group, Max Planck Institute for Brain Research, Max Planck Society, ou_3334049              
4Department: Genes-Circuits-Behavior / Baier, MPI of Neurobiology, Max Planck Society, ou_1128545              

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 Abstract: Vertebrate behavior is strongly influenced by light. Light receptors, encoded by functional opsin proteins, are present inside the vertebrate brain and peripheral tissues. This expression feature is present from fishes to human and appears to be particularly prominent in diurnal vertebrates. Despite their conserved widespread occurrence, the nonvisual functions of opsins are still largely enigmatic. This is even more apparent when considering the high number of opsins. Teleosts possess around 40 opsin genes, present from young developmental stages to adulthood. Many of these opsins have been shown to function as light receptors. This raises the question of whether this large number might mainly reflect functional redundancy or rather maximally enables teleosts to optimally use the complex light information present under water. We focus on tmt-opsin1b and tmt-opsin2, c-opsins with ancestral-type sequence features, conserved across several vertebrate phyla, expressed with partly similar expression in non-rod, non-cone, non-retinal-ganglion-cell brain tissues and with a similar spectral sensitivity. The characterization of the single mutants revealed age- and light-dependent behavioral changes, as well as an impact on the levels of the preprohormone sst1b and the voltage-gated sodium channel subunit scn12aa. The amount of daytime rest is affected independently of the eyes, pineal organ, and circadian clock in tmt-opsin1b mutants. We further focused on daytime behavior and the molecular changes in tmt-opsin1b/2 double mutants, and found that—despite their similar expression and spectral features—these opsins interact in part nonadditively. Specifically, double mutants complement molecular and behavioral phenotypes observed in single mutants in a partly age-dependent fashion. Our work provides a starting point to disentangle the highly complex interactions of vertebrate nonvisual opsins, suggesting that tmt-opsin-expressing cells together with other visual and nonvisual opsins provide detailed light information to the organism for behavioral fine-tuning. This work also provides a stepping stone to unravel how vertebrate species with conserved opsins, but living in different ecological niches, respond to similar light cues and how human-generated artificial light might impact on behavioral processes in natural environments.

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Language(s): eng - English
 Dates: 2019-08-262020-12-102021-01-07
 Publication Status: Published online
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 Identifiers: DOI: 10.1371/journal.pbio.3001012
PMID: 33411725
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Title: PLoS Biol.
  Other : PLoS Biol.
Source Genre: Journal
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Publ. Info: San Francisco, California, US : Public Library of Science
Pages: - Volume / Issue: 19 (1) Sequence Number: e3001012 Start / End Page: - Identifier: ISSN: 1544-9173
CoNE: https://pure.mpg.de/cone/journals/resource/111056649444170