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      Sex‐biased gene expression in the frontal cortex of common marmosets ( Callithrix jacchus) and potential behavioral correlates

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          Abstract

          Introduction

          The common marmoset ( Callithrix jacchus), a small New World monkey, has been widely used as a biological model in neuroscience to elucidate neural circuits involved in cognition and to understand brain dysfunction in neuropsychiatric disorders. In this regard, the availability of gene expression data derived from next‐generation sequencing (NGS) technologies represents an opportunity for a molecular contextualization. Sexual dimorphism account for differences in diseases prevalence and prognosis. Here, we explore sex differences on frontal cortex of gene expression in common marmoset's adults.

          Methods

          Gene expression profiles in six different tissues (cerebellum, frontal cortex, liver, heart, and kidney) were analyzed in male and female marmosets. To emphasize the translational value of this species for behavioral studies, we focused on sex‐biased gene expression from the frontal cortex of male and female in common marmosets and compared to humans ( Homo sapiens).

          Results

          In this study, we found that frontal cortex genes whose expression is male‐biased are conserved between marmosets and humans and enriched with “house‐keeping” functions. On the other hand, female‐biased genes are more related to neural plasticity functions involved in remodeling of synaptic circuits, stress cascades, and visual behavior. Additionally, we developed and made available an application—the CajaDB—to provide a friendly interface for genomic, expression, and alternative splicing data of marmosets together with a series of functionalities that allow the exploration of these data. CajaDB is available at cajadb.neuro.ufrn.br.

          Conclusion

          The data point to differences in gene expression of male and female common marmosets in all tissues analyzed. In frontal cortex, female‐biased expression in synaptic plasticity, stress, and visual processing might be linked to biological and behavioral mechanisms of this sex. Due to the limited sample size, the data here analyzed are for exploratory purposes.

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          Most cited references41

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            The evolution of gene expression levels in mammalian organs.

            Changes in gene expression are thought to underlie many of the phenotypic differences between species. However, large-scale analyses of gene expression evolution were until recently prevented by technological limitations. Here we report the sequencing of polyadenylated RNA from six organs across ten species that represent all major mammalian lineages (placentals, marsupials and monotremes) and birds (the evolutionary outgroup), with the goal of understanding the dynamics of mammalian transcriptome evolution. We show that the rate of gene expression evolution varies among organs, lineages and chromosomes, owing to differences in selective pressures: transcriptome change was slow in nervous tissues and rapid in testes, slower in rodents than in apes and monotremes, and rapid for the X chromosome right after its formation. Although gene expression evolution in mammals was strongly shaped by purifying selection, we identify numerous potentially selectively driven expression switches, which occurred at different rates across lineages and tissues and which probably contributed to the specific organ biology of various mammals.
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              Synaptic plasticity and depression: new insights from stress and rapid-acting antidepressants.

              Depression is a common, devastating illness. Current pharmacotherapies help many patients, but high rates of a partial response or no response, and the delayed onset of the effects of antidepressant therapies, leave many patients inadequately treated. However, new insights into the neurobiology of stress and human mood disorders have shed light on mechanisms underlying the vulnerability of individuals to depression and have pointed to novel antidepressants. Environmental events and other risk factors contribute to depression through converging molecular and cellular mechanisms that disrupt neuronal function and morphology, resulting in dysfunction of the circuitry that is essential for mood regulation and cognitive function. Although current antidepressants, such as serotonin-reuptake inhibitors, produce subtle changes that take effect in weeks or months, it has recently been shown that treatment with new agents results in an improvement in mood ratings within hours of dosing patients who are resistant to typical antidepressants. Within a similar time scale, these new agents have also been shown to reverse the synaptic deficits caused by stress.
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                Author and article information

                Contributors
                mbcsousa@neuro.ufrn.br
                Journal
                Brain Behav
                Brain Behav
                10.1002/(ISSN)2157-9032
                BRB3
                Brain and Behavior
                John Wiley and Sons Inc. (Hoboken )
                2162-3279
                30 October 2018
                December 2018
                : 8
                : 12 ( doiID: 10.1002/brb3.2018.8.issue-12 )
                : e01148
                Affiliations
                [ 1 ] Health Sciences Graduate Program Federal University of Rio Grande do Norte Natal Brazil
                [ 2 ] Bioinformatics Multidisciplinary Environment Federal University of Rio Grande do Norte Natal Brazil
                [ 3 ] Brain Institute, Bioinformatics Multidisciplinary Environment Federal University of Rio Grande do Norte Natal Brazil
                [ 4 ] Brain Institute and Health Sciences Graduate Program Federal University of Rio Grande do Norte Natal Brazil
                Author notes
                [*] [* ] Correspondence

                Maria Bernardete Cordeiro de Sousa, Brain Institute, Federal University of Rio Grande do Norte, Natal, Brazil.

                Email: mbcsousa@ 123456neuro.ufrn.br

                Author information
                http://orcid.org/0000-0001-6196-0046
                http://orcid.org/0000-0001-6979-4951
                http://orcid.org/0000-0001-6200-0418
                Article
                BRB31148
                10.1002/brb3.1148
                6305938
                30378298
                e2473838-79f3-45c8-b5bc-f6f7be5cb35b
                © 2018 Federal Government of Brazil. Brain and Behavior published by Wiley Periodicals, Inc.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 09 November 2017
                : 27 September 2018
                : 30 September 2018
                Page count
                Figures: 4, Tables: 0, Pages: 9, Words: 16786
                Funding
                Funded by: Fundação de Amparo à Pesquisa do Estado do Amazonas
                Award ID: PROPG Edital 010/2015
                Funded by: Conselho Nacional de Desenvolvimento Científico e Tecnológico
                Award ID: CNPq Proc. No. 30.6018/2013‐6
                Funded by: Federal University of Rio Grande do Norte (UFRN)
                Funded by: Brain Institute
                Funded by: Bioinformatics Multidisciplinary Environment (BioME)
                Funded by: NPAD/UFRN
                Categories
                Original Research
                Original Research
                Custom metadata
                2.0
                brb31148
                December 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.5.4 mode:remove_FC converted:26.12.2018

                Neurosciences
                adaptive strategies,database,neuropsychiatric primate model,sexual dimorphism,synaptic plasticity,transcriptomics

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