Department of Nutrition, Genetics and Ethology, Faculty of Veterinary Medicine, Ghent University, Belgium.
J Appl Genet. 2009;50(4):361-9. doi: 10.1007/BF03195694.
Knowledge of in vivo relationship between the coactivator PPARGC1A and its target genes is very limited, especially in the pig. In this study, a real-time PCR experiment was performed on longissimus dorsi muscle (MLD) and backfat with 10 presumed PPARGC1A downstream target genes, involved in energy and fat metabolism, to identify possible relationships with PPARGC1A mRNA expression in vivo in the pig (n = 20). Except for UCP3 and LPL, a very significant difference in expression was found between MLD and backfat for all genes (P < 0.01). Hierarchical cluster analysis and the significant pairing of mRNA expression data between sampling locations suggested a genetic regulation of the expression of several target genes. A positive correlation with PPARGC1A was found for CPT1B, GLUT4, PDK4, and TFAM (P < 0.0001). A negative correlation was found for UCP2, FABP4, LEP (P < 0.0001), and TNF (P = 0.0071). No significant correlation was detected for UCP3 and LPL. This study provides evidence for a clear difference in mRNA expression of crucial genes in fat and energy metabolism between 2 important tissues. Our data suggest a clear impact of PPARGC1A on energy and lipid metabolism in vivo in the pig, through several of these downstream target genes.
关于辅激活因子 PPARGC1A 与其靶基因之间的体内关系,人们知之甚少,尤其是在猪中。本研究通过实时 PCR 实验对长肌(MLD)和背脂进行了检测,涉及 10 个假定的与能量和脂肪代谢相关的 PPARGC1A 下游靶基因,以鉴定其与猪体内 PPARGC1A mRNA 表达之间的可能关系(n=20)。除 UCP3 和 LPL 外,所有基因在 MLD 和背脂之间的表达差异均非常显著(P<0.01)。层次聚类分析和不同采样部位 mRNA 表达数据的显著配对表明,几个靶基因的表达受到遗传调控。CPT1B、GLUT4、PDK4 和 TFAM 与 PPARGC1A 呈正相关(P<0.0001)。UCP2、FABP4、LEP(P<0.0001)和 TNF(P=0.0071)与 PPARGC1A 呈负相关。UCP3 和 LPL 与 PPARGC1A 无显著相关性。本研究为在猪的两种重要组织中,关键脂肪和能量代谢基因的 mRNA 表达存在明显差异提供了证据。我们的数据表明,PPARGC1A 对猪体内的能量和脂质代谢有明显的影响,通过其中的几个下游靶基因。