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Effects of Silencing ACSL1 Gene by siRNA on the Synthesis of Unsaturated Fatty Acids in Adipocytes of Qinchuan Beef Cattle (Bos taurus) |
TIAN Hong-Shan1, SU Xiao-Tong2, ZHAO Zhi-Dong1,*, HAN Xiang-Min1, ZAN Lin-Sen2,3,*, HU Jiang1, LUO Yu-Zhu1, WANG Ji-Qing1, BAI Yan-Bin1 |
1 College of Animal Science and Technology, Gansu Agricultural University/Gansu Key Laboratory of Herbivorous Animal Biotechnology, Lanzhou 730070, China; 2 College of Animal Science and Technology, Northwest A&F University, Yangling 712100, China; 3 National Beef Cattle Improvement Center, Yangling 712100, China |
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Abstract Long-chain acyl-CoA synthetase 1 (ACSL1) is a member of the acyl activating enzyme family, which plays an important role in the activation, transport, degradation and synthesis of fatty acids in vivo. In this study, the adipocytes of Qinchuan beef cattle (Bos taurus) were used as the research object. qRT-PCR and small interfering RNA (siRNA) interference were performed to explore the mechanism of ACSL1 gene on the synthesis of unsaturated fatty acid. Firstly, the temporal expression of ACSL1 gene and unsaturated fatty acid synthesis related genes, such as fatty acid synthase (FASN), stearoyl-CoA desaturease 1 (SCD1), peroxisome proliferator activated receptor gamma (PPARγ), fatty acid desaturase 1 (FADS1) and fatty acid binding protein 3 (FABP3) during adipocyte differentiation were detected, and it was found that the expression levels of ACSL1, FADS1, SCD1, FASN and PPARγ showed a trend of first increasing and then decreasing, and peaked at 4 d, while FABP3 had no significant changes during the differentiation of bovine adipocytes. Then, siRNA targeting the ACSL1 gene was transfected into bovine adipocytes, and found that the mRNA level of ACSL1 was down-regulated by more than 70% (P<0.01), and the protein level was also significantly down-regulated. After silencing the ACSL1 gene, the mRNA level of FABP3 and PPARγ were down-regulated, and FADS1 and FASN were up-regulated, while SCD1 showed a trend of increasing first and then decreasing. Furthermore, interfering ACSL1 gene expression significantly reduced the ratio of C18∶0 (P<0.05), so that the content of saturated fatty acid (SFA) in adipocytes was reduced. Meanwhile, the ratio of C16∶1, C18∶1, C18∶2, arachidonic acid (AA) and eicosapentaenoic acid (EPA) decreased significantly (P<0.01), so that the content of saturated fatty acid (SFA) and polyunsaturated fatty acids (PUFA) in adipocytes was decreased. In addition, Bodipy staining showed that silencing the ACSL1 gene could reduce the formation of lipid droplets in bovine adipocytes. In summary, the ACSL1 gene played an important role in regulating the expression of unsaturated fatty acid synthesis-related genes, fatty acid composition and lipid droplet formation, and provides a theoretical basis for further elucidating the molecular mechanism of unsaturated fatty acid formation in bovine adipocytes.
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Received: 14 February 2020
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Corresponding Authors:
* zhaozd@gsau.edu.cn; zanlinsen@163.com
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[1] 李庆岗, 陶著, 杨玉增, 等. 2012. 长链脂酰CoA合成酶(ACSL)的研究进展[J].中国畜牧兽医, 39(06): 137-140. (Li Q G, Tao Z, Yang Y Z, et al.2012. Research progress of long-chain fatty acyl-CoA synthetase (ACSL)[J]. China Animal Husbandry & Veterinary Medicine, 39(06): 137-140.) [2] 李鹤琼, 罗海玲. 2019. 反刍动物肌内脂肪及脂肪酸调控研究进展[J].中国畜牧杂志, 55(08): 1-5. (Li H Q, Luo H L.2019. Research progress on the regulation of intramuscular fat and fatty acids in ruminants[J]. Chinese Journal of Animal Husbandry, 55(08): 1-5.) [3] 田亚英, 傅念, 吴清. 2018. 长链脂酰辅酶A合成酶及其调控因素的研究及进展[J]. 医学研究杂志, 47(10): 19-21. (Tian Y Y, Fu N, Wu Q.2018. Research and progress on long-chain fatty acyl-CoA synthetase and its regulatory factors[J]. Journal of Medical Research, 47(10): 19-21.) [4] 许会芬. 2016. SREBP-1基因对山羊乳腺上皮细胞脂肪酸代谢的调控作用研究[D]. 博士学位论文, 西北农林科技大学, 导师: 罗军, pp.19-20. (Xu H F.2016. The Regulation function Of SREBP-1 gene on fatty acid metabolism in goat mammary gland epithelial cells[D]. Thesis for Ph.D., Northwest A & F University, Supervisor: Luo J, pp. 19-20.) [5] 赵志东. 2016. 牛ACSL1基因的转录调控研究[D]. 博士学位论文, 西北农林科技大学, 导师: 昝林森, pp.6-7. (Zhao Z D.2016. Transcriptional regulation of bovine ACSL1 gene[D]. Thesis for Ph.D, Northwest A & F University, Supervisor: Zan L S, pp. 6-7.) [6] Amar B S, Chin F K K, Bin D, et al.2016. SREBP2 activation induces hepatic long-chain acyl-CoA synthetase 1 expression in vivo and in vitro through a SRE motif of ACSL1 C-promoter[J]. Journal of Biological Chemistry, 291(10): 5373-5384. [7] Araújo J R, Correiabranco A, Ramalho C, et al.2013. Gestational diabetes mellitus decreases placental uptake of long-chain polyunsaturated fatty acids: Involvement of long-chain acyl-CoA synthetase[J]. Journal of Nutritional Biochemistry, 24(10): 1741-1750. [8] Brasaemle D L, Dolios G, Shapiro L, et al.2004. Proteomic analysis of proteins associated with lipid droplets of basal and lipolytically stimulated 3T3-L1 adipocytes[J]. Journal of Biological Chemistry, 279(45): 46835-46842. [9] Barton L, Kott T, Bures D, et al.2010. The polymorphisms of stearoyl-CoA desaturase (SCD1) and sterol regulatory element binding protein-1 (SREBP-1) genes and their association with the fatty acid profile of muscle and subcutaneous fat in Fleckvieh bulls[J]. 85(1): 15-20. [10] Coleman R A, Lewin T M, Muoio D M.2000. Physiological and nutritional regulation of enzymes of triacylglycerol synthesis[J]. Annual Review of Nutrition, 20(1): 77-103. [11] Cui M, Wang Y, Sun B D, et al.2014. MiR-205 modulates abnormal lipid metabolism of hepatoma cells via targeting acyl-CoA synthetase long-chain family member 1 (ACSL1) mRNA[J]. Biochemical and Biophysical Research Communications, 444(2): 270-275. [12] Cho K H, Kim M J, Jeon G J, et al.2011. Association of genetic variants for FABP3 gene with back fat thickness and intramuscular fat content in pig[J]. Molecular Biology Reports, 38(3): 2161-2166. [13] Cho H P, Nakamura M, Clarke S D.1999. Cloning, expression, and fatty acid regulation of the human delta-5 desaturase[J]. Journal of Biological Chemistry, 274(52): 37335-37339. [14] Ellis J M, Mentock S M, Depetrillo M A, et al.2011. Mouse cardiac acyl coenzyme a synthetase 1 deficiency impairs fatty acid oxidation and induces cardiac hypertrophy[J]. Molecular and Cellular Biology, 31(6): 1252-1262. [15] Golej D L, Askari B, Kramer F, et al.2011. Long-chain acyl-CoA synthetase 4 modulates prostaglandin E2 release from human arterial smooth muscle cells[J]. The Journal of Lipid Research, 52(4): 782-793. [16] Glaser C, Heinrich J, Koletzko B.2010. Role of FADS1 and FADS2 polymorphisms in polyunsaturated fatty acid metabolism[J]. Metabolism-clinical & Experimental, 59(7): 993-999. [17] Hoashi S, Hinenoya T, Tanaka A, et al.2008. Association between fatty acid compositions and genotypes of FABP4 and LXR-alpha in Japanese Black cattle[J]. BMC Genetics, 9(1): 84. [18] Hillebrand M, Søren W G, Lotz-Havla A S, et al.2012. Identification of a new fatty acid synthesis-transport machinery at the peroxisomal membrane[J]. Journal of Biological Chemistry, 287: 210-221. [19] Hannun Y A, Obeid L M.2002. The Ceramide-centric universe of lipid-mediated cell regulation: Stress encounters of the lipid kind[J]. Journal of Biological Chemistry, 277(29): 25847-25850. [20] Joseph R, Poschmann J, Sukarieh R, et al.2015. ACSL1 is associated with fetal programming of insulin sensitivity and cellular lipid content[J]. Molecular Endocrinology, 29(6): 909-920. [21] Lattka E, Illig T, Koletzko B, et al.2010. Genetic variants of the FADS1 FADS2 gene cluster as related to essential fatty acid metabolism[J]. Current Opinion in Lipidology, 21(1): 64-69. [22] Li L O, Grevengoed T J, Paul D S, et al.2014. Compartmentalized Acyl-CoA metabolism in skeletal muscle regulates systemic glucose homeostasis[J]. Diabetes, 64(1): 23-35. [23] Li L O, Mashek D G, An J, et al.2006. Overexpression of rat long chain Acyl-CoA synthetase 1 alters fatty acid metabolism in rat primary hepatocytes[J]. Journal of Biological Chemistry, 281(48): 37246-37255. [24] Li L O, Ellis J M, Paich H A, et al.2009. Liver-specific loss of long chain Acyl-CoA synthetase-1 decreases triacylglycerol synthesis and β-oxidation and alters phospholipid fatty acid composition[J]. Journal of Biological Chemistry, 284(41): 27816-27826. [25] Li C, Aldai N, Vinsky M, et al.2012. Association analyses of single nucleotide polymorphisms in bovine stearoyl-CoA desaturase and fatty acid synthase genes with fatty acid composition in commercial cross-bred beef steers[J]. Animal Genetics, 43(1): 93-97. [26] Massimo B, Loor J J.2008. ACSL1, AGPAT6, FABP3, LPIN1, and SLC27A6 are the most abundant isoforms in bovine mammary tissue and their expression is affected by stage of lactation[J]. The Journal of Nutrition, 138(6): 1019-1024. [27] Marszalek J R, Kitidis C, Dararutana A, et al.2004. Acyl-CoA synthetase 2 overexpression enhances fatty acid internalization and neurite outgrowth[J]. Journal of Biological Chemistry, 279(23): 23882-23891. [28] Miyazaki M, Dobrzyn A, Man W C, et al.2004. Stearoyl-CoA desaturase 1 gene expression is necessary for fructose-mediated induction of lipogenic gene expression by sterol regulatory element-binding protein-1c-dependent and independent mechanisms[J]. Journal of Biological Chemistry, 279(24): 25164-25171. [29] Mukherjee R, Yun J W.2012. Long chain acyl CoA synthetase 1 and gelsolin are oppositely regulated in adipogenesis and lipogenesis[J]. Biochemical and Biophysical Research Communications, 420(3): 588-593. [30] Ntambi J M, Miyazaki M, Stoehr J P, et al.2002. Loss of stearoyl-CoA desaturase-1 function protects mice against adiposity[J]. Proceedings of the National Academy of Sciences of the USA, 99(17): 11482-11486. [31] Oikawa E, Iijima H, Suzuki T, et al.1998. A novel Acyl-CoA synthetase, ACS5, expressed in intestinal epithelial cells and proliferating preadipocytes[J]. Journal of Biochemistry, 124(3): 679-685. [32] Paul A, Watkins.1997. Fatty acid activation[J]. Progress in Lipid Research, 36(1): 55-83. [33] Parkes H A, Preston E, Wilks D, et al.2006. Overexpression of acyl-CoA synthetase-1 increases lipid deposition in hepatic (HepG2) cells and rodent liver in vivo[J]. American Journal of Physiology, 291(4): 737-744. [34] Philipp W, Karin N, Christa K, et al.2011. Association of an ACSL1 gene variant with polyunsaturated fatty acids in bovine skeletal muscle[J]. BMC Genetics, 12(1): 96-96. [35] Siersbaek R, Mandrup S.2011. Transcriptional networks controlling adipocyte differentiation[J]. Cold Spring Harbor Symposia on Quantitative Biology, 76: 247-255. [36] Schoonjans K, Staels B, Auwerx J.1996. Role of the peroxisome proliferator-activated receptor (PPAR) in mediating the effects of fibrates and fatty acids on gene expression[J]. Journal of Lipid Research, 37(5): 907-925. [37] Shi H, Luo J, Zhu J, et al.2013. PPARγ regulates genes involved in triacylglycerol synthesis and secretion in mammary gland epithelial cells of dairy goats[J]. PPAR Research, 2013: 310948. [38] Semenkovich C F.1997. Regulation of fatty acid synthase (FAS)[J]. Progress in Lipid Research, 36(1): 43-53. [39] Schneider H, Staudacher S.2014. Protein mediated fatty acid uptake: Synergy between CD36/FAT-facilitated transport and acyl-CoA synthetase-driven metabolism[J]. Archives of Biochemistry and Biophysics, 546: 8-18. [40] Sugii S, Olson P, Sears D D, et al.2009. PPARgamma activation in adipocytes is sufficient for systemic insulin sensitization[J]. Proceedings of the National Academy of Sciences of the USA, 106(52): 22504-22509. [41] Vergnes L, Beigneux A P, Davis R, et al.2006. Agpat6 deficiency causes subdermal lipodystrophy and resistance to obesity[J]. Journal of Lipid Research, 47(4): 745-754. [42] Whetstone H D, Hurley W L, Davis C L.1986. Identification and characterization of a fatty acid binding protein in bovine mammary gland[J]. Comparative Biochemistry and Physiology Part B: Comparative Biochemistry, 85(3): 687-692. [43] Zulkifli R M, Parr T, Salter A M, et al.2010. Regulation of ovine and porcine stearoyl coenzyme A desaturase gene promoters by fatty acids and sterols[J]. Journal of Animal Science, 88(8): 2565-2575. [44] Zhan T Z, Margarete P, Robert E, et al.2012. Overexpressed FATP1, ACSVL4/FATP4 and ACSL1 increase the cellular fatty acid uptake of 3t3-l1 adipocytes but are localized on intracellular membranes[J]. PLOS ONE, 7(9): e45087. [45] Zhao Z D, Zan L S, Li A N, et al.2016. Characterization of the promoter region of the bovine long-chain acyl-CoA synthetase 1 gene: Roles of E2F1, Sp1, KLF15, and E2F4[J]. Scientific Reports, 6(1): 19661. |
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