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Genetic analysis of abdominal fat distribution in SM/J and A/J mice

机译:SM / J和A / J小鼠腹部脂肪分布的遗传分析

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摘要

Each abdominal fat depot, such as mesenteric or epididymal, differently contributes to the development of insulin resistance. The aim of this study was to identify the genetic regions that contribute to fat accumulation in epididymal/mesenteric fat and to examine whether or not the genetic regions that affect glucose metabolism and body fat distribution are coincident. We previously mapped a major quantitative trait locus (QTL) (T2dm2sa) for impaired glucose tolerance on chromosome 2 and revealed that SM.A-T2dm2sa congenic mice showed not only glucose tolerance but also fat accumulation. In the present study, to identify the loci/genes that control the accumulation of abdominal fat, we perfomed QTL analyses of epididymal/mesenteric fat weight by using (A/J×SM.A-T2dm2sa)F2 mice in which the effect of T2dm2sa was excluded. As a result, two highly significant QTLs for mesenteric fat, as well as three significant QTLs for epididymal/mesenteric fat, were mapped on the different chromosomal regions. This suggests that the fat accumulations in individual fat depots are controlled by distinct genomic regions. Our comparison of these QTLs for abdominal fat distribution with those for glucose metabolism revealed that the major genetic factors affecting body fat distribution do not coincide with genetic factors affecting glucose metabolism in (A/J×SM.A-T2dm2sa)F2.
机译:每个腹部脂肪库,例如肠系膜或附睾,都不同程度地促进了胰岛素抵抗的发展。这项研究的目的是确定有助于附睾/中肠系膜脂肪堆积的遗传区域,并检查影响葡萄糖代谢和体内脂肪分布的遗传区域是否一致。我们先前在2号染色体上绘制了一个主要的定量性状基因座(QTL)(T2dm2sa)用于葡萄糖耐量受损,并揭示了SM.A-T2dm2sa同基因小鼠不仅显示了葡萄糖耐量,而且还显示了脂肪蓄积。在本研究中,为了确定控制腹部脂肪积累的基因座/基因,我们使用(A / J×SM.A-T2dm2sa)F2小鼠对附睾/中肠系膜脂肪重量进行了QTL分析,其中T2dm2sa被排除在外。结果,将肠系膜脂肪的两个高度重要的QTL以及附睾/中肠系膜脂肪的三个重要的QTL定位在不同的染色体区域。这表明单个脂肪库中的脂肪积累受不同的基因组区域控制。我们对这些腹部脂肪分布和葡萄糖代谢QTL的比较发现,影响(A / J×SM.A-T2dm2sa)F2中影响人体脂肪分布的主要遗传因素与影响葡萄糖代谢的遗传因素并不相同。

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