INRA, UMR1079 Systèmes d'Elevage, Nutrition Animale et Humaine, Domaine de la Prise, Saint Gilles, France.
J Anim Breed Genet. 2012 Aug;129(4):316-24. doi: 10.1111/j.1439-0388.2011.00965.x. Epub 2011 Sep 30.
A quantitative trait locus (QTL) affecting fatness in a way opposite to expectations based on breed means was mapped to swine chromosome 7 (SSC7) using crosses between Large White (LW) and Meishan (MS) founders. Defining the molecular fatness trait more explicitly would allow deducing positional candidate genes, for which expression differences must be analysed in experimental populations. First, mRNA levels of genes representing sequential steps in adipogenesis or involved in lipid metabolism were studied in backfat of pigs having homozygous LW(QTL7)/LW(QTL7) or heterozygous LW(QTL7)/MS(QTL7) alleles and considered at two ages. mRNA level of DLK1 expressed in preadipocytes was greater in MS(QTL7)/LW(QTL7) pigs than in homozygous pigs at 28 days. Transcript abundances of CEBPA involved in differentiation, the prolipogenic FASN gene and the adipocyte-specific marker FABP4 were lower in MS(QTL7)/LW(QTL7) pigs compared with LW(QTL7)/LW(QTL7) pigs at 150 days. Because these results suggest a lag time in terminal differentiation associated with the MS allele, seven genes in the QTL interval were deduced as promising candidates for the QTL effect by bioinformatics analysis. Among them, PPARD and CDKN1A had lower expression levels in MS(QTL7)/LW(QTL7) pigs at both ages. Genotype-related differences were observed in mRNA levels of PPARD target genes involved in cell differentiation (FZD7) or fatty acid oxidation (ACADL and ACOX1) at 150 days. These results re-evaluate the potential of PPARD to explain part of variation in pig adiposity.
一个影响肥胖的数量性状位点(QTL)与基于品种均值的预期方向相反,该 QTL 被定位到猪 7 号染色体(SSC7)上,使用长白猪(LW)和梅山猪(MS) founders 进行杂交。更明确地定义分子肥胖性状,可以推导出位置候选基因,需要在实验群体中分析这些基因的表达差异。首先,研究了在具有 LW(QTL7)/LW(QTL7)或 LW(QTL7)/MS(QTL7)杂合等位基因的猪背部脂肪中,代表脂肪生成中连续步骤或参与脂质代谢的基因的 mRNA 水平,并在两个年龄时进行了分析。在 28 天时,在脂肪前体细胞中表达的 DLK1 的 mRNA 水平在 MS(QTL7)/LW(QTL7)猪中高于纯合子猪。在分化中涉及 CEBPA 的转录物丰度、前脂肪生成 FASN 基因和脂肪细胞特异性标记物 FABP4 在 MS(QTL7)/LW(QTL7)猪中低于 LW(QTL7)/LW(QTL7)猪。由于这些结果表明与 MS 等位基因相关的终端分化存在滞后时间,因此通过生物信息学分析推断出 QTL 间隔中的七个基因作为 QTL 效应的有希望的候选基因。其中,在两个年龄时,PPARD 和 CDKN1A 的 mRNA 水平在 MS(QTL7)/LW(QTL7)猪中较低。在 150 天时,PPARD 靶基因参与细胞分化(FZD7)或脂肪酸氧化(ACADL 和 ACOX1)的 mRNA 水平存在与基因型相关的差异。这些结果重新评估了 PPARD 解释猪肥胖部分变异的潜力。