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      Sexual Differentiation of the Rodent Brain: Dogma and Beyond

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          Abstract

          Steroid hormones of gonadal origin act on the neonatal brain to produce sex differences that underlie adult reproductive physiology and behavior. Neuronal sex differences occur on a variety of levels, including differences in regional volume and/or cell number, morphology, physiology, molecular signaling, and gene expression. In the rodent, many of these sex differences are determined by steroid hormones, particularly estradiol, and are established by diverse downstream effects. One brain region that is potently organized by estradiol is the preoptic area (POA), a region critically involved in many behaviors that show sex differences, including copulatory and maternal behaviors. This review focuses on the POA as a case study exemplifying the depth and breadth of our knowledge as well as the gaps in understanding the mechanisms through which gonadal hormones produce lasting neural and behavioral sex differences. In the POA, multiple cell types, including neurons, astrocytes, and microglia are masculinized by estradiol. Multiple downstream molecular mediators are involved, including prostaglandins, various glutamate receptors, protein kinase A, and several immune signaling molecules. Moreover, emerging evidence indicates epigenetic mechanisms maintain sex differences in the POA that are organized perinatally and thereby produce permanent behavioral changes. We also review emerging strategies to better elucidate the mechanisms through which genetics and epigenetics contribute to brain and behavioral sex differences.

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          Hydroxylation of 5-methylcytosine by TET1 promotes active DNA demethylation in the adult brain.

          Cytosine methylation is the major covalent modification of mammalian genomic DNA and plays important roles in transcriptional regulation. The molecular mechanism underlying the enzymatic removal of this epigenetic mark, however, remains elusive. Here, we show that 5-methylcytosine (5mC) hydroxylase TET1, by converting 5mCs to 5-hydroxymethylcytosines (5hmCs), promotes DNA demethylation in mammalian cells through a process that requires the base excision repair pathway. Though expression of the 12 known human DNA glycosylases individually did not enhance removal of 5hmCs in mammalian cells, demethylation of both exogenously introduced and endogenous 5hmCs is promoted by the AID (activation-induced deaminase)/APOBEC (apolipoprotein B mRNA-editing enzyme complex) family of cytidine deaminases. Furthermore, Tet1 and Apobec1 are involved in neuronal activity-induced, region-specific, active DNA demethylation and subsequent gene expression in the dentate gyrus of the adult mouse brain in vivo. Our study suggests a TET1-induced oxidation-deamination mechanism for active DNA demethylation in mammals. Copyright © 2011 Elsevier Inc. All rights reserved.
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            Organizing action of prenatally administered testosterone propionate on the tissues mediating mating behavior in the female guinea pig.

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              Microglia promote the death of developing Purkinje cells.

              The loss of neuronal cells, a prominent event in the development of the nervous system, involves regulated triggering of programmed cell death, followed by efficient removal of cell corpses. Professional phagocytes, such as microglia, contribute to the elimination of dead cells. Here we provide evidence that, in addition to their phagocytic activity, microglia promote the death of developing neurons engaged in synaptogenesis. In the developing mouse cerebellum, Purkinje cells die, and 60% of these neurons that already expressed activated caspase-3 were engulfed or contacted by spreading processes emitted by microglial cells. Apoptosis of Purkinje cells in cerebellar slices was strongly reduced by selective elimination of microglia. Superoxide ions produced by microglial respiratory bursts played a major role in this Purkinje cell death. Our study illustrates a mammalian form of engulfment-promoted cell death that links the execution of neuron death to the scavenging of dead cells.
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                Author and article information

                Journal
                Front Neurosci
                Front. Neurosci.
                Frontiers in Neuroscience
                Frontiers Research Foundation
                1662-4548
                1662-453X
                04 January 2012
                21 February 2012
                2012
                : 6
                : 26
                Affiliations
                [1] 1simpleProgram in Neuroscience and Department of Physiology, University of Maryland School of Medicine Baltimore, MD, USA
                Author notes

                Edited by: Elena Jazin, Uppsala University, Sweden

                Reviewed by: Susan E. Bergeson, Texas Tech University Health Sciences Center, USA; Xi Huang, University of California San Francisco, USA

                *Correspondence: Kathryn M. Lenz, Department of Physiology, University of Maryland School of Medicine, 655 West Baltimore Street, BRB 5-014, Baltimore, 21201 MD, USA. e-mail: kmlenz@ 123456umaryland.edu

                This article was submitted to Frontiers in Neurogenomics, a specialty of Frontiers in Neuroscience.

                Article
                10.3389/fnins.2012.00026
                3282918
                22363256
                0fb4c953-b663-4bb3-a397-99a485dc75b2
                Copyright © 2012 Lenz, Nugent and McCarthy.

                This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.

                History
                : 29 November 2011
                : 04 February 2012
                Page count
                Figures: 3, Tables: 0, Equations: 0, References: 168, Pages: 13, Words: 13347
                Categories
                Neuroscience
                Review Article

                Neurosciences
                estradiol,hormone,development,sex difference,epigenetics,preoptic area
                Neurosciences
                estradiol, hormone, development, sex difference, epigenetics, preoptic area

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