Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Minneapolis, Minnesota, United States of America.
PLoS One. 2009 Dec 24;4(12):e8460. doi: 10.1371/journal.pone.0008460.
Four genome-wide association studies mapped an "obesity" gene to human chromosome 10p11-12. As the zinc finger E-box binding homeobox 1 (ZEB1) transcription factor is encoded by the TCF8 gene located in that region, and as it influences the differentiation of various mesodermal lineages, we hypothesized that ZEB1 might also modulate adiposity. The goal of these studies was to test that hypothesis in mice.
METHODOLOGY/PRINCIPAL FINDINGS: To ascertain whether fat accumulation affects ZEB1 expression, female C57BL/6 mice were fed a regular chow diet (RCD) ad libitum or a 25% calorie-restricted diet from 2.5 to 18.3 months of age. ZEB1 mRNA levels in parametrial fat were six to ten times higher in the obese mice. To determine directly whether ZEB1 affects adiposity, wild type (WT) mice and mice heterozygous for TCF8 (TCF8+/-) were fed an RCD or a high-fat diet (HFD) (60% calories from fat). By two months of age on an HFD and three months on an RCD, TCF8+/- mice were heavier than WT controls, which was attributed by Echo MRI to increased fat mass (at three months on an HFD: 0.517+/-0.081 total fat/lean mass versus 0.313+/-0.036; at three months on an RCD: 0.175+/-0.013 versus 0.124+/-0.012). No differences were observed in food uptake or physical activity, suggesting that the genotypes differ in some aspect of their metabolic activity. ZEB1 expression also increases during adipogenesis in cell culture.
CONCLUSION/SIGNIFICANCE: These results show for the first time that the ZEB1 transcription factor regulates the accumulation of adipose tissue. Furthermore, they corroborate the genome-wide association studies that mapped an "obesity" gene at chromosome 10p11-12.
四项全基因组关联研究将一个“肥胖”基因定位于人类 10 号染色体 p11-12。由于该区域的 TCF8 基因编码锌指 E 盒结合同源盒 1(ZEB1)转录因子,并且它影响各种中胚层谱系的分化,我们假设 ZEB1 也可能调节脂肪量。这些研究的目的是在小鼠中检验该假说。
方法/主要发现:为了确定脂肪积累是否影响 ZEB1 表达,雌性 C57BL/6 小鼠自由摄取常规饮食(RCD)或从 2.5 到 18.3 个月龄时摄取 25%热量限制饮食。肥胖小鼠的参数脂肪中 ZEB1 mRNA 水平高 6 至 10 倍。为了直接确定 ZEB1 是否影响肥胖,野生型(WT)小鼠和 TCF8 杂合(TCF8+/-)小鼠喂食 RCD 或高脂肪饮食(HFD)(60%的热量来自脂肪)。在 HFD 上两个月和 RCD 上三个月时,TCF8+/-小鼠比 WT 对照重,这归因于 Echo MRI 增加了脂肪量(在 HFD 上三个月:0.517+/-0.081 总脂肪/瘦肉比 0.313+/-0.036;在 RCD 上三个月:0.175+/-0.013 与 0.124+/-0.012)。在食物摄入或体力活动方面没有观察到差异,表明基因型在其代谢活动的某些方面存在差异。在细胞培养中脂肪生成过程中 ZEB1 表达也增加。
结论/意义:这些结果首次表明 ZEB1 转录因子调节脂肪组织的积累。此外,它们证实了将“肥胖”基因定位于 10 号染色体 p11-12 的全基因组关联研究。