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      Cold seawater induces early sexual developmental stages in the BPG axis of European eel males

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          Abstract

          Background

          The impossibility of closing the life cycle of the European eel ( Anguilla anguilla) in captivity troubles the future of this critically endangered species. In addition, the European eel is a highly valued and demanded resource, thus the successful closing of its life cycle would have a substantial economic and ecological impact. With the aim of obtaining the highest gamete quality, the study of the effects of environmental factors, such as temperature, on reproductive performance may prove valuable. This is especially true for the exposure to cold water, which has been reported to improve sexual development in multiple other Actinopterygii species.

          Results

          European eel males treated with cold seawater (10 °C, T10) for 2 weeks showed an increase in the proliferation and differentiation of spermatogonial cells until the differentiated spermatogonial type A cell stage, and elevated testosterone and 11-ketotestosterone plasma levels. Transcriptomes from the tissues of the brain-pituitary-gonad (BPG) axis of T10 samples revealed a differential gene expression profile compared to the other experimental groups, with clustering in a principal component analysis and in heat maps of all differentially expressed genes. Furthermore, a functional analysis of differentially expressed genes revealed enriched gene ontology terms involved in the regulation of circadian rhythm, histone modification, meiotic nuclear division, and others.

          Conclusions

          Cold seawater treatment had a clear effect on the activity of the BPG-axis of European eel males. In particular, our cold seawater treatment induces the synchronization and increased proliferation and differentiation of specific spermatogonial cells. In the transcriptomic results, genes related to thermoception were observed. This thermoception may have caused the observed effects through epigenetic mechanisms, since all analysed tissues further revealed differentially expressed genes involved in histone modification. The presented results support our hypothesis that a low temperature seawater treatment induces an early sexual developmental stage in European eels. This hypothesis is logical given that the average temperature experienced by eels in the early stages of their oceanic reproductive migration is highly similar to that of this cold seawater treatment. Further studies are needed to test whether a cold seawater treatment can improve the response of European eels to artificial hormonal treatment, as the results suggest.

          Electronic supplementary material

          The online version of this article (10.1186/s12864-019-5969-6) contains supplementary material, which is available to authorized users.

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          Most cited references59

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          MHC class I: an unexpected role in neuronal plasticity.

          For the nervous system to translate experience into memory and behavior, lasting structural change at synapses must occur. This requirement is clearly evident during critical periods of activity-dependent neural development, and accumulating evidence has established a surprising role for the major histocompatibility complex class I (MHCI) proteins in this process.
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            Regulation of class I MHC gene expression in the developing and mature CNS by neural activity.

            To elucidate molecular mechanisms underlying activity-dependent synaptic remodeling in the developing mammalian visual system, we screened for genes whose expression in the lateral geniculate nucleus (LGN) is regulated by spontaneously generated action potentials present prior to vision. Activity blockade did not alter expression in the LGN of 32 known genes. Differential mRNA display, however, revealed a decrease in mRNAs encoding class I major histocompatibility complex antigens (class I MHC). Postnatally, visually driven activity can regulate class I MHC in the LGN during the final remodeling of retinal ganglion cell axon terminals. Moreover, in the mature hippocampus, class I MHC mRNA levels are increased by kainic acid-induced seizures. Normal expression of class I MHC mRNA is correlated with times and regions of synaptic plasticity, and immunohistochemistry confirms that class I MHC is present in specific subsets of CNS neurons. Finally, beta2-microglobulin, a cosubunit of class I MHC, and CD3zeta, a component of a receptor complex for class I MHC, are also expressed by CNS neurons. These observations indicate that class I MHC molecules, classically thought to mediate cell-cell interactions exclusively in immune function, may play a novel role in neuronal signaling and activity-dependent changes in synaptic connectivity.
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              Functional dynamics of H3K9 methylation during meiotic prophase progression.

              Histone H3 lysine 9 (H3K9) methylation is a crucial epigenetic mark of heterochromatin formation and transcriptional silencing. G9a is a major mammalian H3K9 methyltransferase at euchromatin and is essential for mouse embryogenesis. Here we describe the roles of G9a in germ cell development. Mutant mice in which G9a is specifically inactivated in the germ-lineage displayed sterility due to a drastic loss of mature gametes. G9a-deficient germ cells exhibited perturbation of synchronous synapsis in meiotic prophase. Importantly, mono- and di-methylation of H3K9 (H3K9me1 and 2) in G9a-deficient germ cells were significantly reduced and G9a-regulated genes were overexpressed during meiosis, suggesting that G9a-mediated epigenetic gene silencing is crucial for proper meiotic prophase progression. Finally, we show that H3K9me1 and 2 are dynamically and sex-differentially regulated during the meiotic prophase. This genetic and biochemical evidence strongly suggests that a specific set of H3K9 methyltransferase(s) and demethylase(s) coordinately regulate gametogenesis.
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                Author and article information

                Contributors
                chro4@upvnet.upv.es
                vicgarb4@upvnet.upv.es
                mlpereig@dca.upv.es
                vicgalal@upvnet.upv.es
                juaherj1@upvnet.upv.es
                helge.tveiten@nofima.no
                helge.johnsen@uit.no
                romain.fontaine@nmbu.no
                finn-arne.weltzien@nmbu.no
                jcanizares@upv.es
                (+34) 96 387 93 85 , jfastu@dca.upv.es
                dasncpea@upvnet.upv.es
                Journal
                BMC Genomics
                BMC Genomics
                BMC Genomics
                BioMed Central (London )
                1471-2164
                22 July 2019
                22 July 2019
                2019
                : 20
                : 597
                Affiliations
                [1 ]ISNI 0000 0004 1770 5832, GRID grid.157927.f, Grupo de Acuicultura y Biodiversidad. Instituto de Ciencia y Tecnología Animal, , Universitat Politècnica de València. Edificio 7G, ; Camino de Vera s/n, 46022 Valencia, Spain
                [2 ]ISNI 0000 0004 1770 5832, GRID grid.157927.f, Instituto de Conservación y Mejora de la Agrodiversidad Valenciana, , Universitat Politècnica de València, ; Camino de Vera s/n, 46022 Valencia, Spain
                [3 ]ISNI 0000 0004 0451 2652, GRID grid.22736.32, Norwegian Institute of Fisheries and Food Research, , Nofima AS, ; Muninbakken 9-13, Breivika, 9291 Tromsø, Norway
                [4 ]UiT The Arctic University of Norway, Faculty of Biosciences, Fisheries and Economics, Norwegian College of Fishery Science, Muninbakken 21, N-9037 Tromsø, Norway
                [5 ]ISNI 0000 0004 0607 975X, GRID grid.19477.3c, Department of Basic Sciences and Aquatic Medicine, , Norwegian University of Life Sciences, Faculty of Veterinary Medicine, ; Oslo, Norway
                Author information
                http://orcid.org/0000-0002-6441-5294
                Article
                5969
                10.1186/s12864-019-5969-6
                6647157
                31331264
                ad9bfe2c-71af-49b5-8d11-a1907d8e0c76
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

                History
                : 27 November 2018
                : 11 July 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100010665, H2020 Marie Skłodowska-Curie Actions;
                Award ID: 642893
                Award ID: 642893
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2019

                Genetics
                anguilla anguilla,rna-sequencing,epigenetics,temperature,spermatogonial proliferation,migration,immunofluorescence,radioimmunoassay,histology

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