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      Functional identification of an opsin kinase underlying inactivation of the pineal bistable opsin parapinopsin in zebrafish

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          Abstract

          In the pineal organ of zebrafish larvae, the bistable opsin parapinopsin alone generates color opponency between UV and visible light. Our previous study suggested that dark inactivation of the parapinopsin photoproduct, which activates G-proteins, is important for the regulation of the amount of the photoproduct. In turn, the photoproduct is responsible for visible light sensitivity in color opponency. Here, we found that an opsin kinase or a G-protein-coupled receptor kinase (GRK) is involved in inactivation of the active photoproduct of parapinopsin in the pineal photoreceptor cells of zebrafish larvae. We investigated inactivation of the photoproduct in the parapinopsin cells of various knockdown larvae by measuring the light responses of the cells using calcium imaging. We found that GRK7a knockdown slowed recovery of the response of parapinopsin photoreceptor cells, whereas GRK1b knockdown or GRK7b knockdown did not have a remarkable effect, suggesting that GRK7a, a cone-type GRK, is mainly responsible for inactivation of the parapinopsin photoproduct in zebrafish larvae. We also observed a similar knockdown effect on the response of the parapinopsin photoreceptor cells of mutant larvae expressing the opsin SWS1, a UV-sensitive cone opsin, instead of parapinopsin, suggesting that the parapinopsin photoproduct was inactivated in a way similar to that described for cone opsins. We confirmed the immunohistochemical distribution of GRK7a in parapinopsin photoreceptor cells by comparing the immunoreactivity to GRK7 in GRK7a-knockdown and control larvae. These findings suggest that in pineal photoreceptor cells, the cone opsin kinase GRK7a contributes greatly to the inactivation of parapinopsin, which underlies pineal color opponency.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s40851-021-00171-1.

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          Most cited references41

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          Whole-brain activity mapping onto a zebrafish brain atlas

          In order to localize the neural circuits involved in generating behaviors, it is necessary to assign activity onto anatomical maps of the nervous system. Using brain registration across hundreds of larval zebrafish, we have built an expandable open source atlas containing molecular labels and anatomical region definitions, the Z-Brain. Using this platform and immunohistochemical detection of phosphorylated-Extracellular signal-regulated kinase (ERK/MAPK) as a readout of neural activity, we have developed a system to create and contextualize whole brain maps of stimulus- and behavior-dependent neural activity. This MAP-Mapping (Mitogen Activated Protein kinase – Mapping) assay is technically simple, fast, inexpensive, and data analysis is completely automated. Since MAP-Mapping is performed on fish that are freely swimming, it is applicable to nearly any stimulus or behavior. We demonstrate the utility of our high-throughput approach using hunting/feeding, pharmacological, visual and noxious stimuli. The resultant maps outline hundreds of areas associated with behaviors.
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            Circadian rhythms from multiple oscillators: lessons from diverse organisms.

            The organization of biological activities into daily cycles is universal in organisms as diverse as cyanobacteria, fungi, algae, plants, flies, birds and man. Comparisons of circadian clocks in unicellular and multicellular organisms using molecular genetics and genomics have provided new insights into the mechanisms and complexity of clock systems. Whereas unicellular organisms require stand-alone clocks that can generate 24-hour rhythms for diverse processes, organisms with differentiated tissues can partition clock function to generate and coordinate different rhythms. In both cases, the temporal coordination of a multi-oscillator system is essential for producing robust circadian rhythms of gene expression and biological activity.
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              Prolonged photoresponses in transgenic mouse rods lacking arrestin.

              Arrestins are soluble cytoplasmic proteins that bind to G-protein-coupled receptors, thus switching off activation of the G protein and terminating the signalling pathway that triggers the cellular response. Although visual arrestin has been shown to quench the catalytic activity of photoexcited, phosphorylated rhodopsin in a reconstituted system, its role in the intact rod cell remains unclear because phosphorylation alone reduces the catalytic activity of rhodopsin. Here we have recorded photocurrents of rods from transgenic mice in which one or both copies of the arrestin gene were disrupted. Photoresponses were unaffected when arrestin expression was halved, indicating that arrestin binding is not rate limiting for recovery of the rod photoresponse, as it is in Drosophila. With arrestin absent, the flash response displayed a rapid partial recovery followed by a prolonged final phase. This behaviour indicates that an arrestin-independent mechanism initiates the quench of rhodopsin's catalytic activity and that arrestin completes the quench. The intensity dependence of the photoresponse in rods lacking arrestin further suggests that, although arrestin is required for normal signal termination, it does not participate directly in light adaptation.
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                Author and article information

                Contributors
                terakita@sci.osaka-cu.ac.jp
                Journal
                Zoological Lett
                Zoological Lett
                Zoological Letters
                BioMed Central (London )
                2056-306X
                12 February 2021
                12 February 2021
                2021
                : 7
                : 1
                Affiliations
                [1 ]GRID grid.261445.0, ISNI 0000 0001 1009 6411, Department of Biology and Geosciences, , Graduate School of Science, Osaka City University, ; Osaka, 558-8585 Japan
                [2 ]GRID grid.261445.0, ISNI 0000 0001 1009 6411, The OCU Advanced Research Institute for Natural Science and Technology, , Osaka City University, ; Osaka, 558-8585 Japan
                [3 ]GRID grid.174568.9, ISNI 0000 0001 0059 3836, Department of Chemistry, Biology, and Environmental Science, Faculty of Science, , Nara Women’s University, Kitauoyanishi-machi, ; Nara, 630-8506 Japan
                Article
                171
                10.1186/s40851-021-00171-1
                7881645
                33579376
                13c6dffc-4476-4db1-a483-412ec1222487
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 7 August 2020
                : 27 January 2021
                Funding
                Funded by: Japanese Ministry of Education, Culture, Sports, Science and Technology Grants-in-Aid for Scientific Research
                Award ID: 15H05777
                Award ID: 16K14778
                Award ID: 16KT0074
                Award ID: 17H06015
                Award ID: 18K06336 to
                Award ID: 18K14751
                Award Recipient :
                Funded by: Japan Science and Technology Agency (JST) Core Research for Evolutional Science and Technology (CREST) Grant
                Award ID: JPMJCR1753
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2021

                nonvisual photoreception,pineal organs,bistable opsin,g-protein-coupled receptor kinase,opsin inactivation

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