“…144,163 In pigs, positive association between the IM content and the expressions of myosin (MYL1), adipose-specific phospholipase A2 (AdPLA), melanocortin 4 receptor (MC4R), phosphoenolpyruvated carboxykinase (PEPCK), and SCD, and novel porcine FLJ36031 (pFLJ) genes are suggestive of their role in fast glycolysis and lipid deposition. 142,145 Genomewide-association studies (GWAS) and the liver RNA-Seq on female pigs with extreme phenotypes for IM showed differential expression of transposable elements, long non-coding RNAs. 151,164,165 Furthermore, these studies established the role of putative protein-coding genes including Endotoxin lipopolysaccharide/pro-inflammatory cytokines (LPS/IL-1) in mediating inhibition of retinoid X receptors (RXR) function to regulate cholesterol homeostasis and bile acid homeostasis ( Table 3).…”