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      Transcription Factors in the Regulation of Leydig Cell Gene Expression and Function

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          Abstract

          Cell differentiation and acquisition of specialized functions are inherent steps in events that lead to normal tissue development and function. These processes require accurate temporal, tissue, and cell-specific activation or repression of gene transcription. This is achieved by complex interactions between transcription factors that form a unique combinatorial code in each specialized cell type and in response to different physiological signals. Transcription factors typically act by binding to short, nucleotide-specific DNA sequences located in the promoter region of target genes. In males, Leydig cells play a crucial role in sex differentiation, health, and reproductive function from embryonic life to adulthood. To better understand the molecular mechanisms regulating Leydig cell differentiation and function, several transcription factors important to Leydig cells have been identified, including some previously unknown to this specialized cell type. This mini review summarizes the current knowledge on transcription factors in fetal and adult Leydig cells, describing their roles and mechanisms of action.

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          Most cited references120

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          The Human Transcription Factors

          Transcription factors (TFs) recognize specific DNA sequences to control chromatin and transcription, forming a complex system that guides expression of the genome. Despite keen interest in understanding how TFs control gene expression, it remains challenging to determine how the precise genomic binding sites of TFs are specified and how TF binding ultimately relates to regulation of transcription. This review considers how TFs are identified and functionally characterized, principally through the lens of a catalog of over 1,600 likely human TFs and binding motifs for two-thirds of them. Major classes of human TFs differ markedly in their evolutionary trajectories and expression patterns, underscoring distinct functions. TFs likewise underlie many different aspects of human physiology, disease, and variation, highlighting the importance of continued effort to understand TF-mediated gene regulation.
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            AP-1: a double-edged sword in tumorigenesis.

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              JAK/STAT - Emerging Players in Metabolism.

              The Janus kinase (JAK)/signal transducer and activator of transcription (STAT) pathway is crucial for transducing signals from a variety of metabolically relevant hormones and cytokines including growth hormone, leptin, erythropoietin, IL4, IL6 and IFNγ. A growing body of evidence suggests that this pathway is dysregulated in the context of obesity and metabolic disease. Recent development of animal models has been instrumental in identifying the role of JAK/STAT signaling in the peripheral metabolic organs including adipose, liver, muscle, pancreas, and the immune system. In this review we summarize current knowledge about the function of JAK/STAT proteins in the regulation of metabolism, and highlight new potential therapeutic targets for the treatment of obesity and diabetes.
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                Author and article information

                Contributors
                Journal
                Front Endocrinol (Lausanne)
                Front Endocrinol (Lausanne)
                Front. Endocrinol.
                Frontiers in Endocrinology
                Frontiers Media S.A.
                1664-2392
                07 April 2022
                2022
                : 13
                : 881309
                Affiliations
                [1] 1 Reproduction, Mother and Child Health, Centre de recherche du centre hospitalier universitaire de Québec, Université Laval , Québec City, QC, Canada
                [2] 2 Centre de recherche en Reproduction, Développement et Santé Intergénérationnelle, Department of Obstetrics, Gynecology, and Reproduction, Faculty of Medicine, Université Laval , Québec City, QC, Canada
                Author notes

                Edited by: Vassilios Papadopoulos, University of Southern California, United States

                Reviewed by: Diane Rebourcet, The University of Newcastle, Australia; Peter O’Shaughnessy, University of Glasgow, United Kingdom

                *Correspondence: Jacques J. Tremblay, Jacques-J.Tremblay@ 123456crchudequebec.ulaval.ca

                This article was submitted to Reproduction, a section of the journal Frontiers in Endocrinology

                Article
                10.3389/fendo.2022.881309
                9022205
                35464056
                938abd77-eae4-4261-a80f-300332413483
                Copyright © 2022 de Mattos, Viger and Tremblay

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 22 February 2022
                : 15 March 2022
                Page count
                Figures: 0, Tables: 2, Equations: 0, References: 120, Pages: 10, Words: 4006
                Funding
                Funded by: Canadian Institutes of Health Research , doi 10.13039/501100000024;
                Categories
                Endocrinology
                Mini Review

                Endocrinology & Diabetes
                transcription factors,gene expression,regulatory element,dna binding motif,steroidogenesis,leydig cells

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