Ishikawa Akira
Laboratory of Animal Genetics, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, Aichi, Japan.
PLoS One. 2017 Jan 23;12(1):e0170652. doi: 10.1371/journal.pone.0170652. eCollection 2017.
It is still challenging to identify causal genes governing obesity. Pbwg1.5, a quantitative trait locus (QTL) for resistance to obesity, was previously discovered from wild Mus musculus castaneus mice and was fine-mapped to a 2.1-Mb genomic region of mouse chromosome 2, where no known gene with an effect on white adipose tissue (WAT) has been reported. The aim of this study was to identify a strong candidate gene for Pbwg1.5 by an integration approach of transcriptome analysis (RNA-sequencing followed by real-time PCR analysis) and the causal inference test (CIT), a statistical method to infer causal relationships between diplotypes, gene expression and trait values. Body weight, body composition and biochemical traits were measured in F2 mice obtained from an intercross between the C57BL/6JJcl strain and a congenic strain carrying Pbwg1.5 on the C57BL/6JJcl background. The F2 mice showed significant diplotype differences in 12 traits including body weight, WAT weight and serum cholesterol/triglyceride levels. The transcriptome analysis revealed that Ly75, Pla2r1, Fap and Gca genes were differentially expressed in the liver and that Fap, Ifih1 and Grb14 were differentially expressed in WAT. However, CITs indicated statistical evidence that only the liver Ly75 gene mediated between genotype and WAT. Ly75 expression was negatively associated with WAT weight. The results suggested that Ly75 is a putative quantitative trait gene for the obesity-resistant Pbwg1.5 QTL discovered from the wild M. m. castaneus mouse. The finding provides a novel insight into a better understanding of the genetic basis for prevention of obesity.
识别控制肥胖的因果基因仍然具有挑战性。Pbwg1.5是一个抗肥胖的数量性状位点(QTL),先前是从野生小家鼠栗色小鼠中发现的,并被精细定位到小鼠2号染色体上一个2.1兆碱基的基因组区域,在该区域尚未报道有对白色脂肪组织(WAT)有影响的已知基因。本研究的目的是通过转录组分析(RNA测序,随后进行实时PCR分析)和因果推断测试(CIT)(一种推断双倍型、基因表达和性状值之间因果关系的统计方法)的整合方法,确定Pbwg1.5的一个强候选基因。对从C57BL/6JJcl品系与在C57BL/6JJcl背景上携带Pbwg1.5的近交系杂交获得的F2小鼠进行体重、身体组成和生化性状测量。F2小鼠在包括体重、WAT重量和血清胆固醇/甘油三酯水平在内的12个性状上表现出显著的双倍型差异。转录组分析显示,Ly75、Pla2r1、Fap和Gca基因在肝脏中差异表达,Fap、Ifih1和Grb14在WAT中差异表达。然而,CIT表明只有肝脏Ly75基因在基因型和WAT之间起介导作用,这具有统计学证据。Ly75表达与WAT重量呈负相关。结果表明,Ly75是从野生小家鼠栗色小鼠中发现的抗肥胖Pbwg1.5 QTL的一个假定数量性状基因。这一发现为更好地理解预防肥胖的遗传基础提供了新的见解。