College of Animal Science and Technology, Northeast Agricultural University, Harbin, 150030, P. R. China.
Poult Sci. 2010 Nov;89(11):2341-50. doi: 10.3382/ps.2010-00857.
Chicken peroxisome proliferator-activated receptor γ (PPARγ), which is highly expressed in adipose tissues, is a key factor in fat accumulation in the abdominal fat pad. In this study, association and pairwise epistasis analyses were performed for all the polymorphisms detected in PPARγ and for 9 genes from PPARγ-correlated lipid metabolic pathways for abdominal fat weight (AFW) in 10th-generation populations of Northeast Agricultural University broiler lines divergently selected for abdominal fat content. Epistatic networks were then reconstructed with the identified epistatic effects. Single-marker association analyses showed that 5 of the 20 screened polymorphisms were significantly associated with AFW (P < 0.05), and CCAAT/enhancer-binding protein α (C/EBPα) c.552G>A was 1 of the 5 significant loci. Pairwise interaction analyses showed that 15 pairs of polymorphisms reached a significance level of P < 2.64 × 10(-4) (adjusted by Bonferroni correction) in the lean line, 41 pairs reached significance in the fat line, and 7 pairs reached significance in both lines. Interestingly, many other loci interacted with C/EBPα c.552G>A in both lines. In epistatic network analyses, C/EBPα c.552G>A seemed to behave as a hub for the epistatic network in both lines. All these results revealed that the genetic architecture of C/EBPα c.552G>A for AFW seemed to be an apparent individual main-effect QTL but that it could be dissected into a genetic epistatic network. Our results suggest that C/EBPα c.552G>A might be the most important locus contributing to phenotypic variation in AFW among all the polymorphisms detected in this study.
鸡过氧化物酶体增殖物激活受体 γ(PPARγ)在脂肪组织中高度表达,是腹部脂肪垫脂肪堆积的关键因素。在这项研究中,对 PPARγ 中检测到的所有多态性以及与 PPARγ 相关的脂质代谢途径中的 9 个基因进行了关联和成对上位性分析,以研究腹部脂肪重量(AFW)在东北农业大学肉鸡系的第 10 代群体中的差异选择。然后用鉴定出的上位性效应重建上位性网络。单标记关联分析显示,20 个筛选的多态性中有 5 个与 AFW 显著相关(P < 0.05),CCAAT/增强子结合蛋白α(C/EBPα)c.552G>A 是 5 个显著位点之一。成对互作分析显示,在瘦肉系中,有 15 对多态性达到了显著水平(P < 2.64×10(-4),经 Bonferroni 校正调整),在脂肪系中达到了 41 对,在两条系中达到了 7 对。有趣的是,在两条系中,许多其他的基因座与 C/EBPα c.552G>A 互作。在上位性网络分析中,C/EBPα c.552G>A 似乎在两条系的上位性网络中表现为一个枢纽。所有这些结果表明,C/EBPα c.552G>A 对 AFW 的遗传结构似乎是一个明显的个体主效 QTL,但它可以被分解为一个遗传上位性网络。我们的研究结果表明,C/EBPα c.552G>A 可能是本研究中检测到的所有多态性中对 AFW 表型变异贡献最大的基因座。