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      Programming of adipose tissue miR-483-3p and GDF-3 expression by maternal diet in type 2 diabetes

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          Abstract

          Nutrition during early mammalian development permanently influences health of the adult, including increasing the risk of type 2 diabetes and coronary heart disease. However, the molecular mechanisms underlying such programming are poorly defined. Here we demonstrate that programmed changes in miRNA expression link early-life nutrition to long-term health. Specifically, we show that miR-483-3p is upregulated in adipose tissue from low-birth-weight adult humans and prediabetic adult rats exposed to suboptimal nutrition in early life. We demonstrate that manipulation of miR-483-3p levels in vitro substantially modulates the capacity of adipocytes to differentiate and store lipids. We show that some of these effects are mediated by translational repression of growth/differentiation factor-3, a target of miR-483-3p. We propose that increased miR-483-3p expression in vivo, programmed by early-life nutrition, limits storage of lipids in adipose tissue, causing lipotoxicity and insulin resistance and thus increasing susceptibility to metabolic disease.

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          Origins and Mechanisms of miRNAs and siRNAs.

          Over the last decade, approximately 20-30 nucleotide RNA molecules have emerged as critical regulators in the expression and function of eukaryotic genomes. Two primary categories of these small RNAs--short interfering RNAs (siRNAs) and microRNAs (miRNAs)--act in both somatic and germline lineages in a broad range of eukaryotic species to regulate endogenous genes and to defend the genome from invasive nucleic acids. Recent advances have revealed unexpected diversity in their biogenesis pathways and the regulatory mechanisms that they access. Our understanding of siRNA- and miRNA-based regulation has direct implications for fundamental biology as well as disease etiology and treatment.
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            Adipose tissue expandability, lipotoxicity and the Metabolic Syndrome--an allostatic perspective.

            While the link between obesity and type 2 diabetes is clear on an epidemiological level, the underlying mechanism linking these two common disorders is not as clearly understood. One hypothesis linking obesity to type 2 diabetes is the adipose tissue expandability hypothesis. The adipose tissue expandability hypothesis states that a failure in the capacity for adipose tissue expansion, rather than obesity per se is the key factor linking positive energy balance and type 2 diabetes. All individuals possess a maximum capacity for adipose expansion which is determined by both genetic and environmental factors. Once the adipose tissue expansion limit is reached, adipose tissue ceases to store energy efficiently and lipids begin to accumulate in other tissues. Ectopic lipid accumulation in non-adipocyte cells causes lipotoxic insults including insulin resistance, apoptosis and inflammation. This article discusses the links between adipokines, inflammation, adipose tissue expandability and lipotoxicity. Finally, we will discuss how considering the concept of allostasis may enable a better understanding of how diabetes develops and allow the rational design of new anti diabetic treatments. Copyright (c) 2009 Elsevier B.V. All rights reserved.
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              Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops.

              Imprinted genes are expressed from only one of the parental alleles and are marked epigenetically by DNA methylation and histone modifications. The paternally expressed gene insulin-like growth-factor 2 (Igf2) is separated by approximately 100 kb from the maternally expressed noncoding gene H19 on mouse distal chromosome 7. Differentially methylated regions in Igf2 and H19 contain chromatin boundaries, silencers and activators and regulate the reciprocal expression of the two genes in a methylation-sensitive manner by allowing them exclusive access to a shared set of enhancers. Various chromatin models have been proposed that separate Igf2 and H19 into active and silent domains. Here we used a GAL4 knock-in approach as well as the chromosome conformation capture technique to show that the differentially methylated regions in the imprinted genes Igf2 and H19 interact in mice. These interactions are epigenetically regulated and partition maternal and paternal chromatin into distinct loops. This generates a simple epigenetic switch for Igf2 through which it moves between an active and a silent chromatin domain.
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                Author and article information

                Journal
                Cell Death Differ
                Cell Death Differ
                Cell Death and Differentiation
                Nature Publishing Group
                1350-9047
                1476-5403
                June 2012
                06 January 2012
                1 June 2012
                : 19
                : 6
                : 1003-1012
                Affiliations
                [1 ]simpleMRC Toxicology Unit , Lancaster Road, Leicester LE1 9HN, UK
                [2 ]simpleUniversity of Cambridge Metabolic Research Laboratories and Department of Clinical Biochemistry, Institute of Metabolic Science, Addenbrooke's Hospital , Cambridge CB2 0QQ, UK
                [3 ]Koch Institute for Integrative Cancer Research, Massachussets Institue of Technology, Cambridge, MA, USA
                [4 ]simpleSteno Diabetes Centre , Niels Steensens Vej 2, DK-2820 Gentofte, Denmark
                Author notes
                [* ]simpleMRC Toxicology Unit , Lancaster Road, Leicester LE1 9HN, UK. Tel: +44 (0)116 252 5544; Fax: +44 (0)116 252 5616; E-mail: aew5@ 123456le.ac.uk (AEW) or mb446@ 123456le.ac.uk (MB)
                [* ]simpleUniversity of Cambridge Metabolic Research Laboratories and Department of Clinical Biochemistry, Institute of Metabolic Science, Addenbrooke's Hospital , Cambridge CB2 0QQ, UK. Tel: +44 (0)122 333 6792; Fax: +44 (0)122 333 0598; E-mail: ks14@ 123456cam.ac.uk (KS) or seo10@ 123456cam.ac.uk (SEO)
                [5]

                These authors contributed equally to this work.

                Article
                cdd2011183
                10.1038/cdd.2011.183
                3354052
                22223106
                66318171-9319-4ac8-a995-23db71ad99fd
                Copyright © 2012 Macmillan Publishers Limited

                This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/

                History
                : 26 September 2011
                : 01 November 2011
                : 02 November 2011
                Categories
                Original Paper

                Cell biology
                mir-483,nutritional programming,maternal diet,gdf3,translational control,microrna
                Cell biology
                mir-483, nutritional programming, maternal diet, gdf3, translational control, microrna

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