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C57BL/6J mice as a polygenic developmental model of diet‐induced obesity

Susceptibility to obesity changes during the course of life. We utilized the C57BL/6J (B6) and 129S mouse as a genetic model for variation in diet‐induced obesity to define the adiposity phenotypes from birth to maturity at 8 weeks‐of‐age. From birth to 8 weeks‐of‐age, both male and female 129S mice...

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Autores principales: Chu, Dinh‐Toi, Malinowska, Elzbieta, Jura, Magdalena, Kozak, Leslie P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392500/
https://www.ncbi.nlm.nih.gov/pubmed/28400497
http://dx.doi.org/10.14814/phy2.13093
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author Chu, Dinh‐Toi
Malinowska, Elzbieta
Jura, Magdalena
Kozak, Leslie P.
author_facet Chu, Dinh‐Toi
Malinowska, Elzbieta
Jura, Magdalena
Kozak, Leslie P.
author_sort Chu, Dinh‐Toi
collection PubMed
description Susceptibility to obesity changes during the course of life. We utilized the C57BL/6J (B6) and 129S mouse as a genetic model for variation in diet‐induced obesity to define the adiposity phenotypes from birth to maturity at 8 weeks‐of‐age. From birth to 8 weeks‐of‐age, both male and female 129S mice had significantly higher fat mass and adiposity index than B6 mice, although they were not obese. After 8 weeks‐of‐age, B6 had greater adiposity/obesity than 129S mice in response to a high fat (HF). We sought to determine the mechanism activating the fat accumulation in B6 mice at 8‐weeks‐of‐age. We used microarray analysis of gene expression during development of inguinal fat to show that molecular networks of lipogenesis were maximally expressed at 8 weeks‐of‐age. In addition, the DNA methylation analysis of the Sfrp5 promoter and binding of acetylated histones to Sfrp5 and Acly promoter regions showed that major differences in the expression of genes of lipogenesis and chromatin structure occur during development. Differences in lipogenesis networks could account for the strain‐dependent differences in adiposity up to 8 weeks‐of‐age; however, changes in the expression of genes in these networks were not associated with the susceptibility to DIO in B6 male mice beyond 8 weeks‐of‐age.
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spelling pubmed-53925002017-04-17 C57BL/6J mice as a polygenic developmental model of diet‐induced obesity Chu, Dinh‐Toi Malinowska, Elzbieta Jura, Magdalena Kozak, Leslie P. Physiol Rep Original Research Susceptibility to obesity changes during the course of life. We utilized the C57BL/6J (B6) and 129S mouse as a genetic model for variation in diet‐induced obesity to define the adiposity phenotypes from birth to maturity at 8 weeks‐of‐age. From birth to 8 weeks‐of‐age, both male and female 129S mice had significantly higher fat mass and adiposity index than B6 mice, although they were not obese. After 8 weeks‐of‐age, B6 had greater adiposity/obesity than 129S mice in response to a high fat (HF). We sought to determine the mechanism activating the fat accumulation in B6 mice at 8‐weeks‐of‐age. We used microarray analysis of gene expression during development of inguinal fat to show that molecular networks of lipogenesis were maximally expressed at 8 weeks‐of‐age. In addition, the DNA methylation analysis of the Sfrp5 promoter and binding of acetylated histones to Sfrp5 and Acly promoter regions showed that major differences in the expression of genes of lipogenesis and chromatin structure occur during development. Differences in lipogenesis networks could account for the strain‐dependent differences in adiposity up to 8 weeks‐of‐age; however, changes in the expression of genes in these networks were not associated with the susceptibility to DIO in B6 male mice beyond 8 weeks‐of‐age. John Wiley and Sons Inc. 2017-04-11 /pmc/articles/PMC5392500/ /pubmed/28400497 http://dx.doi.org/10.14814/phy2.13093 Text en © 2017 Institute of Animal Reproduction and Food Research of the Polish Academy of Sciences. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Chu, Dinh‐Toi
Malinowska, Elzbieta
Jura, Magdalena
Kozak, Leslie P.
C57BL/6J mice as a polygenic developmental model of diet‐induced obesity
title C57BL/6J mice as a polygenic developmental model of diet‐induced obesity
title_full C57BL/6J mice as a polygenic developmental model of diet‐induced obesity
title_fullStr C57BL/6J mice as a polygenic developmental model of diet‐induced obesity
title_full_unstemmed C57BL/6J mice as a polygenic developmental model of diet‐induced obesity
title_short C57BL/6J mice as a polygenic developmental model of diet‐induced obesity
title_sort c57bl/6j mice as a polygenic developmental model of diet‐induced obesity
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392500/
https://www.ncbi.nlm.nih.gov/pubmed/28400497
http://dx.doi.org/10.14814/phy2.13093
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