DOI QR코드

DOI QR Code

Cloning of OLR1 Gene in Pig Adipose Tissue and Preliminary Study on Its Lipid-accumulating Effect

  • Sun, Chao (College of Animal Science and Technology, Northwest A&F University) ;
  • Liu, Chun-wei (College of Animal Science and Technology, Northwest A&F University) ;
  • Zhang, Zhong-pin (College of Animal Science and Technology, Northwest A&F University)
  • Received : 2009.02.16
  • Accepted : 2009.06.04
  • Published : 2009.10.01

Abstract

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. OLR1 expression profile in different tissues of pig was analyzed. Finally, we studied the correlation between OLR1 and lipid metabolism related genes including peroxisome proliferator-activated $receptor{\gamma}2$ ($PPAR{\gamma}2$), fatty acid synthetase (FAS), triacylglycerol hydrolase (TGH), CAAT/enhancer binding protein $\alpha$ ($C/EBP{\alpha}$) 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 OLR1 in pig lung was exceedingly higher than other tested tissues (p<0.01). In pig adipose tissue, the expression level of OLR1 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 $PPAR{\gamma}2$, FAS and SREBP-1c, but not TGH or C/EBP${\alpha}$. In conclusion, OLR1 was highly associated with fat deposition and its transcription, as suggested by high correlations, was possibly regulated by $PPAR{\gamma}2$ and SREBP-1c.

Keywords

References

  1. Chen, M., S. Narumiya, T. Masaki and T. Sawamura. 2001, Conserved C-terminal residues within the lectin-like domain of LOX-1 are essential for oxidized low-density-lipoprotein binding, Biochem. J 355:289-296 https://doi.org/10.1042/0264-6021:3550289
  2. Chen, M., T. Masaki and T. Sawamura. 2002, LOX-1, the receptor for oxidized low-density lipoprotein identified from endothelial cells: implications in endothelial dysfunction and atherosclerosis, Pharmacol. Ther 95:89-100 https://doi.org/10.1016/S0163-7258(02)00236-X
  3. Chen, X. P. and GH. Du. 2007, Lectin-like oxidized low-density lipoprotein receptor-1: protein, ligands, expression and pathophysiological significance, Chin. Med. J 120:421-426
  4. Chen, X. P., T. T. Zhang and DH. Du. 2007, Lectin-like oxidized low-density lipoprotein receptor-1, a new promising target for the therapy of atherosclerosis? Cardiovasc. Drug Rev 25:146-161 https://doi.org/10.1111/j.1527-3466.2007.00009.x
  5. Chui, P. C., H. P. Guan, M. Lehrke, M. Lehrke and M. A. Lazar. 2005, PPAR gamma regulates adipocyte cholesterol metabolism via oxidized LDL receptor 1. Clin. Invest 115:2244-2256 https://doi.org/10.1172/JCI24130
  6. Constance, C. M., J. I. Morgan and R. M. Umek. 1996, C/EBP alpha regulation of the growth-arrest-associated gene gadd45, Mol. Cell. Biol 16:3878-3883
  7. Ferre, P. and F. Foufelle. 2007, SREBP-1c transcription factor and lipid homeostasis: Clinical perspective, Horm. Res 68:72-82 https://doi.org/10.1159/000100426
  8. Gondret, F., P. Ferre and I. Dugail. 2001, ADD-1/ SREBP-1 is a major determinant of tissue differential lipogenic capacity in mammalian and avian species, J. Lipid Res 42:106-113
  9. Hausman, G. J. 2003, Dexamethasone induced preadipocyte recruitment and expression of CCAAT/enhancing binding protein α and peroxisome proliferator activated receptpr-γ proteins in porcine stromal-vascular (S-V) cell cultures obtained before and after the onset of fetal adipogenesis, Gen. Comp.Endocrinol 130:61-70
  10. Hollenberg, A. N., V. S. Susulic, J. P. Madura, B. Zhang, D. E. Moller, P. Tontonoz, P. Sarraf, B. M. Spiegelman and B. B. Lowell. 1997, Functional antagonism between CCAAT/ enhancer binding protein-αand peroxisome proliferatorsactivated receptor-γ on the leptin promoter, J. Biol. Chem 272:5283-5290 https://doi.org/10.1074/jbc.272.8.5283
  11. Hsu, M. H., S. S. Chirala and S. J. Wakil. 1996, Human fatty- acid synthase gene, Biol. Chem. 271:13584-13592 https://doi.org/10.1074/jbc.271.23.13584
  12. Laplante, M., W. T. Festuccia, G. Soucy, Y. Gelinas, J. Lalonde, J. P. Berger and Y. Deshaies. 2006, Mechanisms of the depot specificity of peroxisome proliferator- Activated receptor $\gamma$ action on adipose tissue metabolism, Diabetes 55:2771-2778 https://doi.org/10.2337/db06-0551
  13. Larsen, T. M., S. Toubro and A. Astrup. 2003, PPARgamma agonists in the treatment of type II diabetes: is increased fatness commensurate with long-term efficacy, Int. J. Obes27:147-161 https://doi.org/10.1038/sj.ijo.802223
  14. Mathieu, L., T. F. William, S. Genevieve, G. Yves, L. Josee, P. B. Joel and D. Yves. 2006, Mechanisms of the depot specificity of peroxisome proliferator-Activated receptor $\gamma$ action on adipose tissue metabolism, Diabetes 55:2771-2778 https://doi.org/10.2337/db06-0551
  15. Matsuda, M., B. S. Korn, R. E. Hammer, Y. A. Moon, R. Komuro, J. D. Horton, J. L. Goldstein, M. S. Brown and I. Shimomura. 2001, SREBP cleavage- activating protein (SCAP) is required for increased lipid synthesis in liver induced by cholesterol deprivation and insulin elevation, Genes Dev 15:1206-1216 https://doi.org/10.1101/gad.891301
  16. May-Yun Wang, Paul Grayburn, Shuyuan Chen, Mariella Ravazzola, Lelio Orci and Roger H. Unger. 2008, Adipogenic capacity and the susceptibility to type 2 diabetes and metabolic syndrome, PNAS 105:6139-6144 https://doi.org/10.1073/pnas.0801981105
  17. Rawson, R. B. 2003, Control of lipid metabolism by regulated intramembrane proteolysis of sterol. Regulatory element binding proteins (SREBPs), Biochem. Soc. Symp 70:221-231
  18. Reiter, S. S., C. H. Halsey, B. M. Stronacha, J. L. Bartosha, W. K. Owsleya and W. G. Bergen. 2007, Lipid metabolism related gene-expression profiling in liver, skeletal muscle and adipose tissue in crossbred Duroc and Pietrain pigs, Comp. Biochem. Physiol. Part D: Genomics Proteomics 200-206
  19. Roder, K., L. Zhang and M. Schweizer. 2007, SREBP-1c mediates the retinoid-dependent increase in fatty acid synthase promoter activity in HepG2, FEBS Lett 581:2715-2720 https://doi.org/10.1016/j.febslet.2007.05.022
  20. Ronald, L. M., S. T. Ding, E. O'B. Smith and H. J. Mersmann. 2000, Expression of porcine adipocyte transcripts during differentiation in vitro and in vivo, Comp. Biochem. Physiol. Part B, Biochem. Mol. Biol 126:291-302 https://doi.org/10.1016/S0305-0491(00)00185-1
  21. Sawamura, T., N. Kume, T. Aoyama, H. Moriwaki, H. Hoshikawa, Y. Aiba, T. Tanaka, S. Miwa, Y. Katsura, T. Kita and T. Masaki. 1997, An endothelial receptor for oxidized low-density lipoprotein, Nature 386:73-77 https://doi.org/10.1038/386073a0
  22. Schweizer, M., K. Roder, L. Zhang and S. S. Wolf. 2002, Transcription factors acting on the promoter of the rat fatty acid synthase gene, Biochem. Soc. Trans. 30:1070-1072 https://doi.org/10.1042/BST0301070
  23. Sekiya, M., N. Yahagi, T. Matsuzaka, Y. Takeuchi, Y. Nakagawa, H. Takahashi, H. Okazaki, Y. Iizuka, K. Ohashi, T. Gotoda, S. Ishibashi, R. Nagai, T. Yamazaki, T. Kadowaki, N. Yamada, J. Osuga and H. Shimano. 2007, SREBP-1-independent regulation of lipogenic gene expression in adipocytes, J. Lipid Res 48:1581-1591 https://doi.org/10.1194/jlr.M700033-JLR200
  24. Sharma, A. M. and B. Staels. 2007, Peroxisome proliferatoractivated receptor and adipose tissue - Understanding obesity- Related changes in regulation of lipid and glucose metabolism, J. Clin. Endocrinol. Metab 92:386-395 https://doi.org/10.1210/jc.2006-1268
  25. Wei, E. H., W. H. Gao and R. Lehner. 2007, Attenuation of adipocyte triacylglycerol hydrolase activity decreases basal fatty acid efflux, J. Biol. Chem 282:8027-8035 https://doi.org/10.1074/jbc.M605789200
  26. Wei, E. H., M. Alam, F. C. Sun, L. B. Agellon, D. E. Vance and R. Lehner. 2007, Apolipoprotein B and triacylglycerol secretion in human triacylglycerol hydrolase transgenic mice, J. Lipid Res 48:2597-2606 https://doi.org/10.1194/jlr.M700320-JLR200
  27. Werman, A., A. Hollenberg, G. Solanes, C. Bjorbaek, A. J. Vidal- Puig and J. S. Flier. 1997, Ligand-independent activation domain in the N terminus of peroxisome proliferatorsactivated receptor$\gamma$ (PPAR$\gamma$) J. Biol. Chem 272:20230-20235 https://doi.org/10.1074/jbc.272.32.20230
  28. Yamanaka, S., X. Y. Zhang, K. Miura, S. Kim and H. Iwao. 1998, The human gene encoding the lectin-type oxidized LDL receptor (OLR1) is a novel member of the natural killer gene complex with a unique expression profile. Genomics 54:191-199 https://doi.org/10.1006/geno.1998.5561

Cited by

  1. Analysis of the oxidized low density lipoprotein receptor 1 gene as a potential marker for carcass quality traits in Qinchuan cattle vol.32, pp.1, 2019, https://doi.org/10.5713/ajas.18.0079