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Investigation of the role of epigenetic modification of the rat glucokinase gene in fetal programming

Bogdarina, Irina, Murphy, Helena C., Burns, Shamus P. and Clark, Adrian J.L. (2004) Investigation of the role of epigenetic modification of the rat glucokinase gene in fetal programming. Life Science, 74 (11). pp. 1407-1415. ISSN 0024-3205

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    Abstract

    Fetal malnutrition is associated with development of impaired glucose tolerance, diabetes and hypertension in later life in humans and several mammalian species. The mechanisms that underlie this phenomenon of fetal programming are unknown. We hypothesize that adverse effects in utero and early life may influence the basal expression levels of certain genes such that they are re-set with long-term consequences for the organism. An excellent candidate mechanism for this re-setting process is DNA methylation, since post-natal methylation patterns are largely established in utero. We have sought to test this hypothesis by investigating the glucokinase gene (Gck) in rat offspring programmed using a maternal low protein diet model (MLP). Northern blot reveals that fasting levels of Gck expression are reduced after programming, although this distinction disappears after feeding. Bisulphite sequencing of the hepatic Gck promoter indicates a complete absence of methylation at the 12 CpG sites studied in controls and MLP animals. Non-expressing cardiac tissue also showed no DNA methylation in this region, whereas brain and all fetal tissues were fully methylated. These findings are not consistent with the hypothesis that programming results from differential methylation of Gck. However, it remains possible that programming may influence methylation patterns in Gck at a distance from the promoter, or in genes encoding factors that regulate basal Gck expression.

    Item Type: Article
    Additional Information: © 2003 Elsevier Inc. All rights reserved.
    Uncontrolled Keywords: Fetal programming; Fetal malnutrition; Glucokinase; Diabetes Mellitus; DNA methylation
    Subjects: Q Science > Q Science (General)
    Q Science > QR Microbiology
    Schools: School of Applied Sciences
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    Depositing User: Sara Taylor
    Date Deposited: 20 Dec 2007
    Last Modified: 28 Jul 2010 19:20
    URI: http://eprints.hud.ac.uk/id/eprint/204

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