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      The expression profile of a multi-stress inducible transient receptor potential vanilloid 4 (TRPV4) in Pacific oyster Crassostrea gigas

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          Highlights

          • 1

            CgTRPV4 with typical structural characteristics was indentified from Crassostrea gigas.

          • 2

            CgTRPV4 was located in both endoplasmic reticulum and cytoplasmic membrane of oyster haemocytes.

          • 3

            CgTRPV4 mRNA was ubiquitously expressed with the highest level in gill.

          • 4

            The expression of CgTRPV4 mRNA was significantly up-regulated after high temperature stress at 30°C or V. splendidus stimulation.

          Abstract

          Transient receptor potential vanilloid 4 (TRPV4) is one of the major non-selective cation channel proteins, which plays a crucial role in sensing biotic and abiotic stresses, such as pathogen infection, temperature, mechanical pressure and osmotic pressure changes by regulating Ca 2+ homeostasis. In the present study, a TRPV4 homologue was identified in Pacific oyster Crassostrea gigas, designated as CgTRPV4. The open reading frame (ORF) of CgTRPV4 was of 2298 bp encoding a putative polypeptide of 765 amino acid residues with three typical ankyrin domains and six conserved transmembrane domains of TRPV4 subfamily proteins, as well as multiple N-glycosylation sites, cAMP- and cGMP-dependent protein kinase phosphorylation sites, protein kinase C phosphorylation sites, casein kinase II phosphorylation sites, and prokaryotic membrane lipoprotein lipid attachment site. The deduced amino acid sequence of CgTRPV4 shared 20.5%-26.2% similarity with TRPV4s from other species. During the early ontogenesis stages of oyster, the mRNA transcripts of CgTRPV4 were detectable in all the stages with the highest expression level in fertilized eggs and the lowest in D-hinged larvae. In adult oyster, the CgTRPV4 mRNA could be detected in all the examined tissues, including gill, hepatopancreas, adductor muscle, labial palp, mantle and haemocyte, with the highest expression level in gill (45.08-fold of that in hepatopancreas, p < 0.05). In immunocytochemical assay, the CgTRPV4 positive signals were distributed in both endoplasmic reticulum and cytoplasmic membrane of oyster haemocytes. The mRNA expression of CgTRPV4 in gill was significantly up-regulated after high temperature stress at 30°C ( p < 0.05) and after Vibrio splendidus stimulation ( p < 0.05). These results indicated that CgTRPV4 was a classical member of TRPV4 family in oyster, which was induced by either biotic or abiotic stimulations and involved in mediating the stress response of oysters.

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          Most cited references47

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          The oyster genome reveals stress adaptation and complexity of shell formation.

          The Pacific oyster Crassostrea gigas belongs to one of the most species-rich but genomically poorly explored phyla, the Mollusca. Here we report the sequencing and assembly of the oyster genome using short reads and a fosmid-pooling strategy, along with transcriptomes of development and stress response and the proteome of the shell. The oyster genome is highly polymorphic and rich in repetitive sequences, with some transposable elements still actively shaping variation. Transcriptome studies reveal an extensive set of genes responding to environmental stress. The expansion of genes coding for heat shock protein 70 and inhibitors of apoptosis is probably central to the oyster's adaptation to sessile life in the highly stressful intertidal zone. Our analyses also show that shell formation in molluscs is more complex than currently understood and involves extensive participation of cells and their exosomes. The oyster genome sequence fills a void in our understanding of the Lophotrochozoa.
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            Transient receptor potential cation channels in disease.

            The transient receptor potential (TRP) superfamily consists of a large number of cation channels that are mostly permeable to both monovalent and divalent cations. The 28 mammalian TRP channels can be subdivided into six main subfamilies: the TRPC (canonical), TRPV (vanilloid), TRPM (melastatin), TRPP (polycystin), TRPML (mucolipin), and the TRPA (ankyrin) groups. TRP channels are expressed in almost every tissue and cell type and play an important role in the regulation of various cell functions. Currently, significant scientific effort is being devoted to understanding the physiology of TRP channels and their relationship to human diseases. At this point, only a few channelopathies in which defects in TRP genes are the direct cause of cellular dysfunction have been identified. In addition, mapping of TRP genes to susceptible chromosome regions (e.g., translocations, breakpoint intervals, increased frequency of polymorphisms) has been considered suggestive of the involvement of these channels in hereditary diseases. Moreover, strong indications of the involvement of TRP channels in several diseases come from correlations between levels of channel expression and disease symptoms. Finally, TRP channels are involved in some systemic diseases due to their role as targets for irritants, inflammation products, and xenobiotic toxins. The analysis of transgenic models allows further extrapolations of TRP channel deficiency to human physiology and disease. In this review, we provide an overview of the impact of TRP channels on the pathogenesis of several diseases and identify several TRPs for which a causal pathogenic role might be anticipated.
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              Sensing with TRP channels.

              Drosophila melanogaster flies carrying the trp (transient receptor potential) mutation are rapidly blinded by bright light, because of the absence of a Ca2+-permeable ion channel in their photoreceptors. The identification of the trp gene and the search for homologs in yeast, flies, worms, zebrafish and mammals has led to the discovery of a large superfamily of related cation channels, named TRP channels. Activation of TRP channels is highly sensitive to a variety of chemical and physical stimuli, allowing them to function as dedicated biological sensors that are essential in processes such as vision, taste, tactile sensation and hearing.
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                Author and article information

                Contributors
                Journal
                Fish Shellfish Immunol Rep
                Fish Shellfish Immunol Rep
                Fish and Shellfish Immunology Reports
                Elsevier
                2667-0119
                15 August 2022
                December 2022
                15 August 2022
                : 3
                : 100064
                Affiliations
                [a ]Liaoning Key Laboratory of Marine Animal Immunology & Disease Control, Dalian Ocean University, 52 Heishijiao Street, Dalian 116023, China
                [b ]Liaoning Key Laboratory of Marine Animal Immunology, Dalian Ocean University, Dalian 116023, China
                [c ]Dalian Key Laboratory of Aquatic Animal Disease Prevention and Control, Dalian Ocean
                Author notes
                [* ]Corresponding authors at: Liaoning Key Laboratory of Marine Animal Immunology & Disease Control, Dalian Ocean University, 52 Heishijiao Street, Dalian 116023, China. yangchuanyan@ 123456dlou.edu.cn
                [** ]Corresponding author. linglingwang@ 123456dlou.edu.cn
                Article
                S2667-0119(22)00014-7 100064
                10.1016/j.fsirep.2022.100064
                9680104
                36419610
                7fbbbcb8-290a-4f08-87c8-4edd77bd46ca
                © 2022 The Author(s). Published by Elsevier Ltd.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 5 August 2022
                : 11 August 2022
                : 12 August 2022
                Categories
                Article

                crassostrea gigas,transient receptor potential vanilloid 4,expression profile,high temperature stress,vibrio splendidus stimulation

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