Scientia Agricultura Sinica ›› 2013, Vol. 46 ›› Issue (18): 3894-3900.doi: 10.3864/j.issn.0578-1752.2013.18.020

• ANIMAL SCIENCE·VETERINARY SCIENCERE·SOURCE INSECT • Previous Articles     Next Articles

Profiling of Differential Expressed MicroRNA in Intramuscular Fat and Subcutaneous Fat of Simmental and Bioinformatic Analyses of miR-27b Target Gene

 WANG  Hai-Yang, ZHENG  Yue, LI  Hui-Xia, HAN  Zhao-Yu, WANG  Gen-Lin   

  1. College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095
  • Received:2013-03-04 Online:2013-09-15 Published:2013-05-13

Abstract: 【Objective】 In order to explore the role of microRNA in the growth and development process and its regulatory mechanism in intramuscular fat, the profiling of differential expressed microRNA in intramuscular fat and subcutaneous fat of Simmental were analyzed by microarray and real-time PCR (qRT-PCR). The target genes and signal pathway of miRNA-27b were predicted by bioinformatics software and database.【Method】Microarray of bovine microRNA was employed to detect the differentially expressed microRNA between intramuscular adipose tissue and subcutaneous adipose tissue. Then the expression of four selected microRNAs (miR-140, miR-145, miR-143 and miR-27b) in intramuscular adipose and subcutaneous adipose was also validated by qRT-PCR method. Target scan algorithm was used to predict target gene of miR-27b, and the result of gene set was analyzed by bioinformatics of GO annotations, GO term enrichment and KEGG enrichment methods. 【Result】 It was revealed that there were 88 microRNAs with significant differential expression between bovine intramuscular fat and subcutaneous fat (P<0.01). The expression of miR-140, miR-145, miR-143 and miR-27b which were also detected by qRT-PCR was in high concordance with microarray results. The results of bioinformatics indicated that target genes of miR-27b were mostly enrichment in MAPK, Wnt, Hedgehog, TGF-beta, GnRH signaling pathway, especially in MAPK pathway. 【Conclusion】There are specific microRNA expression profiles in bovine intramuscular adipose tissue and subcutaneous adipose tissue. Some differentially high expressed microRNA in intramuscular adipose tissue such as miR-27b may play important roles by distinct pathway in bovine intramuscular adipogenesis.

Key words: intramuscular fat , differential microRNA , target genes , signal pathway

[1]Nishimura T, Hattori A, Takahashi K. Structural changes in intramuscular connective tissue during the fattening of Japanese black cattle: effect of marbling on beef tenderization. Journal of Animal Science, 1999, 77(1): 93-104.

[2]Ambros V. The functions of animal microRNAs. Nature, 2004, 431(7006): 350-355.

[3]Esau C, Kang X, Peralta E, Hanson E, Marcusson E G, Ravichandran L V, Sun Y, Koo S, Perera R J, Jain R, Dean N M, Freier S M, Bennett C F, Lollo B, Griffey R. MicroRNA-143 regulates adipocyte differentiation. Journal of Biological Chemistry, 2004, 279(50): 52361-52365.

[4]Kajimoto K, Naraba H, Iwai N. MicroRNA and 3T3-L1 pre-adipocyte differentiation. RNA-A Publication of The RNA Society, 2006, 12(9): 1626-1632.

[5]Tam Tam S, Bastian I, Zhou XF, Vander Hoek M, Michael MZ, Gibbins IL, Haberberger RV. MicroRNA-143 expression in dorsal root ganglion neurons. Cell Tissue Research, 2011, 346(2): 163-173.

[6]Jin W, Dodson M V, Moore SS, Basarab J A, Guan L L. Characterization of microRNA expression in bovine adipose tissues: a potential regulatory mechanism of subcutaneous adipose tissue development. BMC Molecular Biology, 2010, 11: 29.

[7]Li H Y, Xi Q Y, Xiong Y Y, Liu X L, Cheng X, Shu G, Wang S B, Wang L N, Gao P, Zhu X T, Jiang Q Y, Yuan L, Zhang Y L. Identification and comparison of microRNAs from skeletal muscle and adipose tissues from two porcine breeds. Animal Genetics, 2012, 43(6): 704-713.

[8]Klöting N, Berthold S, Kovacs P, Schön M R, Fasshauer M, Ruschke K, Stumvoll M, Blüher M. MicroRNA expression in human omental and subcutaneous adipose tissue. PloS One, 2009, 4(3): 4699-4703.

[9]Guo Y, Chen Y, Zhang Y, Zhang Y, Chen L, Mo D. Up-regulated miR-145 expression inhibits porcine preadipocytes differentiation by targeting IRS1. International Journal of Biological Macromolecules, 2012, 8(10): 1408-1417.

[10]Li H, Zhang Z, Zhou X, Wang Z, Wang G, Han Z. Effects of MicroRNA-143 in the differentiation and proliferation of bovine intramuscular preadipocytes. Molecul Biology Reporter, 2011, 38(7): 4273-4280.

[11]Qin L, Chen Y, Niu Y, Chen W, Wang Q, Xiao S, Li A, Xie Y, Li J, Zhao X, He Z, Mo D. A deep investigation into the adipogenesis mechanism: profile of microRNAs regulating adipogenesis by modulating the canonical Wnt/beta-catenin signaling pathway. BMC Genomics, 2010, 11: 320.

[12]Gu Z, Eleswarapu S, Jiang H. Identification and characterization of microRNAs from the bovine adipose tissue and mammary gland. Febs Letters, 2007, 581(5): 981-988.

[13]Chen CZ, Li L, Lodish HF, Bartel DP. MicroRNAs modulate hematopoietic lineage differentiation. Science, 2004, 303(5654): 83-86.

[14]Lin Q, Gao Z, Alarcon RM, Ye J, Yun Z. A role of miR-27 in the regulation of adipogenesis. Febs Journal, 2009, 276(8): 2348-2358.

[15]Wang T, Li M, Guan J, Li P, Wang H, Guo Y, Shuai S, Li X. MicroRNAs miR-27a and miR-143 regulate porcine adipocyte lipid metabolism. International Journal of Molecular Sciences, 2011, 12(11): 7950-7959.

[16]Ji J, Zhang J, Huang G,Qian J, Wang X, Mei S. Over-expressed microRNA-27a and 27b influence fat accumulation and cell proliferation during rat hepatic stellate cell activation. Febs Letters, 2009, 583(4): 759-766.

[17]Karbiener M, Fischer C, Nowitsch S, Opriessnig P, Papak C, Ailhaud G, Dani C, Amri EZ, Scheideler M. microRNA miR-27b impairs human adipocyte differentiation and targets PPARγ. Biochemical and Biophysical Research Communications, 2009, 390(2): 247-251.

[18]Kimura I, Konishi M, Asaki T, Furukawa N, Ukai K, Mori M, Hirasawa A, Tsujimoto G, Ohta M, Itoh N, Fujimoto M. Neudesin, an extracellular heme-binding protein, suppresses adipogenesis in 3T3-L1 cells via the MAPK cascade. Biochemical and Biophysical Research Communications, 2009, 381(1): 75-80.

[19]Wang M, Wang JJ, Li J, Park K, Qian X, Ma JX, Zhang SX. Pigment epithelium-derived factor suppresses adipogenesis via inhibition of the MAPK/ERK pathway in 3T3-L1 preadipocytes. American Journal of Physiology-Endocrinology and Metabolism, 2009, 297(6): E1378-1387.

[20]Bowers RR, Lane MD. Wnt signaling and adipocyte lineage commitment. Cell Cycle, 2008, 7(9): 1191-1196.

[21]Prestwich TC, Macdougald OA. Wnt/beta-catenin signaling in adipogenesis and metabolism. Current Opinion in Cell Biology, 2007, 19(6): 612-617.

[22]Kennell JA, MacDougald OA. Wnt signaling inhibits adipogenesis through beta-catenin-dependent and-independent mechanisms. Journal of  Biological Chemistry, 2005, 280(25): 24004-24010.

[23]Li HX, Luo X, Liu RX, Yang YJ, Yang GS. Roles of Wnt/β-catenin signaling in adipogenic differentiation potential of adipose-derived mesenchymal stem cells. Molecular and Cellular Endocrinology, 2008, 291(1-2): 116-124.

[24]Suh JM, Gao X, McKay J, McKay R, Salo Z, Graff JM. Hedgehog signaling plays a conserved role in inhibiting fat formation. Cell Metabolism, 2006, 3(1): 25-34.

[25]Li G, Li Y, Li X, Ning X, Li M, Yang G. MicroRNA Identity and Abundance in Developing Swine Adipose Tissue as Determined by Solexa Sequencing. Journal of Cellular Biochemistry, 2011, 112(5): 1318-1328.

[26]Takanabe R, Ono K, Abe Y, Takaya T, Horie T, Wada H, Kita T, Satoh N, Shimatsu A, Hasegawa K. Up-regulated expression of microRNA-143 in association with obesity in adipose tissue of mice fed high-fat diet. Biochemical and Biophysical Research Communications, 2008, 376(4): 728-732.
[1] PAN DaoXing, WANG Zhen, YANG MaoLin, LIAO QiaoPing, YANG ChangPing, WU YuPing, WANG JinZhou, LIU RuoYu. Association of the PPARγ and C/EBPα Gene Expression with Intramuscular Fat Content in Different Varieties of Pig [J]. Scientia Agricultura Sinica, 2017, 50(1): 171-182.
[2] ZHANG Xin-chen, ZHAO Qi-ling, CHEN Meng-meng, SUN Jia-rui, BAO En-dong, ZHANG Shu-xia, Lü Ying-jun. Signal Pathway of Interferon-β Induced by Porcine Circovirus Type 2 in PK-15 Cells [J]. Scientia Agricultura Sinica, 2016, 49(10): 2008-2016.
[3] ZHAO Jing-xian, LI Juan, YAN Xing-rong, NI He-min, CHEN Yan, ZHANG Lu-pei, GAO Hui-jiang, XU Shang-zhong, LI Jun-ya1, GAO Xue. The Biological Identification of FABP4 Transgenic Cattle [J]. Scientia Agricultura Sinica, 2014, 47(24): 4895-4903.
[4] LI Guo-Xi, WANG Le-Le, SUN Gui-Rong, KANG Xiang-Tao. Tissue Expression Profile and Bioinformatics Analysis of Abundance miR-101 from the Hypothalamus of Chicken [J]. Scientia Agricultura Sinica, 2013, 46(6): 1247-1255.
[5] CHEN Yang, HUANG Zheng-Yang, ZHANG Yang, LI Xin-Yu, ZHEN Ting, WU Ning-Zhao, XU Qi, CHEN Guo-Hong. Molecular Cloning and Preliminary Functional Analysis of Domains of Duck Retinoic Acid Inducible Gene I [J]. Scientia Agricultura Sinica, 2013, 46(10): 2094-2102.
[6] LIAO Fang-Fang, YUAN Si-Chun, ZHANG Zhong-Wen, WU Guo-Juan. Constructions of Arkadia and UCH37 Expression Vectors and Effects on TGF-β1/Smad7 Signal Pathway [J]. Scientia Agricultura Sinica, 2012, 45(9): 1848-1856.
[7] FENG Shao-Zhen, LI Jiao, WU Xiao-Chan, CAO Wei-Sheng, LIAO Ming. The Function of PI3K/Akt Signal Pathway During ALV-J Infection in DF-1 Cells [J]. Scientia Agricultura Sinica, 2011, 44(16): 3446-3453.
[8] HUANG Ye-Chuan, HE Zhi-Fei, LI Hong-Jun, QIN Gang, WANG Ting, MA Ming-Hui. The Flavor Contribution of Subcutaneous and Intramuscular Fat to Pork [J]. Scientia Agricultura Sinica, 2011, 44(10): 2118-2130.
[9] ZHANG Hong-yu,SHAN An-shan,XU Lin,LI Jian-ping,CHENG Bao-jing
. Effects of Protein Restriction in Sows During Lactation on Serum Lipids, the Content of Intramuscular Fat, and H-FABP mRNA Expression in the Filial Pigs#br# [J]. Scientia Agricultura Sinica, 2010, 43(6): 1229-1234 .
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!