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      Behavioral phenotyping of a rat model of the BDNF Val66Met polymorphism reveals selective impairment of fear memory

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          Abstract

          The common brain-derived neurotrophic factor (BDNF) Val66Met polymorphism is associated with reduced activity-dependent BDNF release and increased risk for anxiety disorders and PTSD. Here we behaviorally phenotyped a novel Val66Met rat model with an equivalent valine to methionine substitution in the rat Bdnf gene (Val68Met). In a three-day fear conditioning protocol of fear learning and extinction, adult rats with the Met/Met genotype demonstrated impaired fear memory compared to Val/Met rats and Val/Val controls, with no genotype differences in fear learning or extinction. This deficit in fear memory occurred irrespective of the sex of the animals and was not seen in adolescence (4 weeks of age). There were no changes in open-field locomotor activity or anxiety measured in the elevated plus maze (EPM) nor in other types of memory measured using the novel-object recognition test or Y-maze. BDNF exon VI expression in the dorsal hippocampus was higher and BDNF protein level in the ventral hippocampus was lower in female Val/Met rats than female Val/Val rats, with no other genotype differences, including in total BDNF, BDNF long, or BDNF IV mRNA. These data suggest a specific role for the BDNF Met/Met genotype in fear memory in rats. Further studies are required to investigate gene–environment interactions in this novel animal model.

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          The BDNF val66met Polymorphism Affects Activity-Dependent Secretion of BDNF and Human Memory and Hippocampal Function

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            Genetic variant BDNF (Val66Met) polymorphism alters anxiety-related behavior.

            A common single-nucleotide polymorphism in the brain-derived neurotrophic factor (BDNF) gene, a methionine (Met) substitution for valine (Val) at codon 66 (Val66Met), is associated with alterations in brain anatomy and memory, but its relevance to clinical disorders is unclear. We generated a variant BDNF mouse (BDNF(Met/Met)) that reproduces the phenotypic hallmarks in humans with the variant allele. BDNF(Met) was expressed in brain at normal levels, but its secretion from neurons was defective. When placed in stressful settings, BDNF(Met/Met) mice exhibited increased anxiety-related behaviors that were not normalized by the antidepressant, fluoxetine. A variant BDNF may thus play a key role in genetic predispositions to anxiety and depressive disorders.
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              Genome sequence of the Brown Norway rat yields insights into mammalian evolution.

              The laboratory rat (Rattus norvegicus) is an indispensable tool in experimental medicine and drug development, having made inestimable contributions to human health. We report here the genome sequence of the Brown Norway (BN) rat strain. The sequence represents a high-quality 'draft' covering over 90% of the genome. The BN rat sequence is the third complete mammalian genome to be deciphered, and three-way comparisons with the human and mouse genomes resolve details of mammalian evolution. This first comprehensive analysis includes genes and proteins and their relation to human disease, repeated sequences, comparative genome-wide studies of mammalian orthologous chromosomal regions and rearrangement breakpoints, reconstruction of ancestral karyotypes and the events leading to existing species, rates of variation, and lineage-specific and lineage-independent evolutionary events such as expansion of gene families, orthology relations and protein evolution.
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                Author and article information

                Contributors
                e.jaehne@latrobe.edu.au
                Journal
                Transl Psychiatry
                Transl Psychiatry
                Translational Psychiatry
                Nature Publishing Group UK (London )
                2158-3188
                7 March 2022
                7 March 2022
                2022
                : 12
                : 93
                Affiliations
                [1 ]GRID grid.1018.8, ISNI 0000 0001 2342 0938, Department of Psychology and Counselling, School of Psychology and Public Health, , La Trobe University, ; Melbourne, Australia
                [2 ]GRID grid.1018.8, ISNI 0000 0001 2342 0938, Department of Biochemistry and Genetics, La Trobe Institute for Molecular Science, , La Trobe University, ; Melbourne, Australia
                [3 ]GRID grid.4708.b, ISNI 0000 0004 1757 2822, Department of Pharmacological and Biomolecular Sciences, , University of Milan, ; Milan, Italy
                [4 ]GRID grid.419422.8, Biological Psychiatry Laboratory, , IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, ; Brescia, Italy
                [5 ]GRID grid.17088.36, ISNI 0000 0001 2150 1785, Department of Translational Neuroscience, College of Human Medicine, , Michigan State University, ; Grand Rapids, USA
                [6 ]GRID grid.477988.d, ISNI 0000 0004 0453 6689, Hauenstein Neuroscience Center, , Mercy Health Saint Mary’s, ; Grand Rapids, USA
                [7 ]GRID grid.1008.9, ISNI 0000 0001 2179 088X, Department of Pharmacology, , University of Melbourne, ; Melbourne, Australia
                [8 ]GRID grid.1011.1, ISNI 0000 0004 0474 1797, College of Public Health, Medical and Veterinary Sciences, , James Cook University, ; Townsville, Australia
                Author information
                http://orcid.org/0000-0002-6376-9170
                http://orcid.org/0000-0002-6428-9128
                http://orcid.org/0000-0003-3678-5244
                http://orcid.org/0000-0002-1699-5060
                http://orcid.org/0000-0003-2571-6753
                http://orcid.org/0000-0002-7555-3799
                Article
                1858
                10.1038/s41398-022-01858-5
                8901920
                35256586
                469934b0-7e92-4b84-89fd-42ca6b689c82
                © The Author(s) 2022

                Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 18 October 2021
                : 10 February 2022
                : 16 February 2022
                Categories
                Article
                Custom metadata
                © The Author(s) 2022

                Clinical Psychology & Psychiatry
                neuroscience,psychiatric disorders
                Clinical Psychology & Psychiatry
                neuroscience, psychiatric disorders

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