Changes in gene expression associated with FTO overexpression in mice.

Single nucleotide polymorphisms in the first intron of the fat-mass-and-obesity-related gene FTO are associated with increased body weight and adiposity. Increased expression of FTO is likely underlying this obesity phenotype, as mice with two additional copies of Fto (FTO-4 mice) exhibit increased...

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Main Authors: Myrte Merkestein, James S McTaggart, Sheena Lee, Holger B Kramer, Fiona McMurray, Mathilde Lafond, Lily Boutens, Roger Cox, Frances M Ashcroft
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4026227?pdf=render
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spelling doaj-f7d9621211284f279eac8dedde570dbb2020-11-25T02:49:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0195e9716210.1371/journal.pone.0097162Changes in gene expression associated with FTO overexpression in mice.Myrte MerkesteinJames S McTaggartSheena LeeHolger B KramerFiona McMurrayMathilde LafondLily BoutensRoger CoxFrances M AshcroftSingle nucleotide polymorphisms in the first intron of the fat-mass-and-obesity-related gene FTO are associated with increased body weight and adiposity. Increased expression of FTO is likely underlying this obesity phenotype, as mice with two additional copies of Fto (FTO-4 mice) exhibit increased adiposity and are hyperphagic. FTO is a demethylase of single stranded DNA and RNA, and one of its targets is the m6A modification in RNA, which might play a role in the regulation of gene expression. In this study, we aimed to examine the changes in gene expression that occur in FTO-4 mice in order to gain more insight into the underlying mechanisms by which FTO influences body weight and adiposity. Our results indicate an upregulation of anabolic pathways and a downregulation of catabolic pathways in FTO-4 mice. Interestingly, although genes involved in methylation were differentially regulated in skeletal muscle of FTO-4 mice, no effect of FTO overexpression on m6A methylation of total mRNA was detected.http://europepmc.org/articles/PMC4026227?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Myrte Merkestein
James S McTaggart
Sheena Lee
Holger B Kramer
Fiona McMurray
Mathilde Lafond
Lily Boutens
Roger Cox
Frances M Ashcroft
spellingShingle Myrte Merkestein
James S McTaggart
Sheena Lee
Holger B Kramer
Fiona McMurray
Mathilde Lafond
Lily Boutens
Roger Cox
Frances M Ashcroft
Changes in gene expression associated with FTO overexpression in mice.
PLoS ONE
author_facet Myrte Merkestein
James S McTaggart
Sheena Lee
Holger B Kramer
Fiona McMurray
Mathilde Lafond
Lily Boutens
Roger Cox
Frances M Ashcroft
author_sort Myrte Merkestein
title Changes in gene expression associated with FTO overexpression in mice.
title_short Changes in gene expression associated with FTO overexpression in mice.
title_full Changes in gene expression associated with FTO overexpression in mice.
title_fullStr Changes in gene expression associated with FTO overexpression in mice.
title_full_unstemmed Changes in gene expression associated with FTO overexpression in mice.
title_sort changes in gene expression associated with fto overexpression in mice.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Single nucleotide polymorphisms in the first intron of the fat-mass-and-obesity-related gene FTO are associated with increased body weight and adiposity. Increased expression of FTO is likely underlying this obesity phenotype, as mice with two additional copies of Fto (FTO-4 mice) exhibit increased adiposity and are hyperphagic. FTO is a demethylase of single stranded DNA and RNA, and one of its targets is the m6A modification in RNA, which might play a role in the regulation of gene expression. In this study, we aimed to examine the changes in gene expression that occur in FTO-4 mice in order to gain more insight into the underlying mechanisms by which FTO influences body weight and adiposity. Our results indicate an upregulation of anabolic pathways and a downregulation of catabolic pathways in FTO-4 mice. Interestingly, although genes involved in methylation were differentially regulated in skeletal muscle of FTO-4 mice, no effect of FTO overexpression on m6A methylation of total mRNA was detected.
url http://europepmc.org/articles/PMC4026227?pdf=render
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