Cloning of OLR1 gene in pig adipose tissue and preliminary study on its lipid-accumulating effect.

In this study we cloned and characterized a novel lipid-accumulating gene, the oxidized low-density lipoprotein receptor 1 (OLR1), which is associated with lipogenesis. We analyzed the gene structure and detected the mRNA transcriptional expression levels in pig adipose tissues at different months of age (MA) and in different economic types (lean type and obese type) using real-time fluorescence quantitative PCR. OLRI expression profile in different tissues of pig was analyzed. Finally, we studied the correlation between OLRI and lipid metabolism related genes including peroxisome proliferator-activated receptorγ2 (PPARγ2), fatty acid synthetase (FAS), triacylglycerol hydrolase (TGH), CAAT/enhancer binding protein α (C/EBPα) and sterol regulatory element binding protein-1c (SREBP-1c). Results indicated that the OLR1 gene of the pig exhibited the highest homology with the cattle (84%), and the lowest with the mouse (27%). The signal peptide located from amino acid 38 to 60 and the domain from amino acid 144 to 256 were shared by the C-type lectin family. The expression level of OLRI in pig lung was exceedingly higher than other tested tissues (p<0.01). In pig adipose tissue, the expression level of OLRI mRNA increased significantly with growth (p<0.01). The expression level of OLR1 mRNA in obese-type pigs was significantly higher than that of lean-type pigs of the same monthly age (p<0.05). In adipose tissue, the expression of OLR1 correlated with PPARγ2, FAS and SREBP-1c, but not TGH or C/EBPα. In conclusion, OLRI was highly associated with fat deposition and its transcription, as suggested by high correlations, was possibly regulated by PPARγ2 and SREBP-1c.