MicroRNA-21 regulates PI3K/Akt/mTOR signaling by targeting TGFβI during skeletal muscle development in pigs

PLoS ONE

Volumn 10, Issue 5, 2015, Pages

  Bai, Lijing ^a   Liang, Ruyi ^a   Yang, Yalan ^a   Hou, Xinhua ^a   Wang, Zishuai ^a   Zhu, Shiyun ^a   Wang, Chuduan ^b   Tang, Zhonglin ^a   Li, Kui ^a  

^a INSTITUTE OF PLANT PROTECTION   (China)

^b CHINA AGRICULTURAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

MAMMALIAN TARGET OF RAPAMYCIN; MICRORNA; MICRORNA 21; PROTEIN KINASE; TRANSFORMING GROWTH FACTOR BETA1; UNTRANSLATED RNA; PHOSPHATIDYLINOSITOL 3 KINASE; PROTEIN KINASE B; TARGET OF RAPAMYCIN KINASE; TRANSFORMING GROWTH FACTOR BETA;

ANIMAL EXPERIMENT; ARTICLE; BIOINFORMATICS; CONTROLLED STUDY; DEVELOPMENTAL STAGE; DOWN REGULATION; GENE EXPRESSION; MUSCLE DEVELOPMENT; NONHUMAN; PERINATAL PERIOD; PIG; PRENATAL PERIOD; QUANTITATIVE ANALYSIS; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SKELETAL MUSCLE; UPREGULATION; WESTERN BLOTTING; ANIMAL; CELL CULTURE; GENE EXPRESSION REGULATION; GENETICS; GROWTH, DEVELOPMENT AND AGING; METABOLISM; MOLECULAR GENETICS; SEQUENCE ANALYSIS; SIGNAL TRANSDUCTION;

SUIDAE;

ANIMALS; CELLS, CULTURED; GENE EXPRESSION REGULATION, DEVELOPMENTAL; MICRORNAS; MOLECULAR SEQUENCE DATA; MUSCLE, SKELETAL; PHOSPHATIDYLINOSITOL 3-KINASES; PROTO-ONCOGENE PROTEINS C-AKT; SEQUENCE ANALYSIS, RNA; SIGNAL TRANSDUCTION; SWINE; TOR SERINE-THREONINE KINASES; TRANSFORMING GROWTH FACTOR BETA;

EID: 84929096301     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0119396     Document Type: Article

References (51)

1. Bartel D P MicroRNAs: genomics, biogenesis, mechanism, and function. Cell. 2004; 116(2): 281-97. PMID: 14744438
2. He L, Hannon G J MicroRNAs: small RNAs with a big role in gene regulation. Nat Rev Genet. 2004; 5 (7): 522-31. PMID: 15211354
3. Chen Jian Fu, M Elizabeth M, T J Michael, Wu Qiulian, C Thomas E, H Scott M, et al. The role of micro- RNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation. Nat Genet.2006; 38(2): 228-233. PMID: 16380711
4. McCarthy J J MicroRNA-206: the skeletal muscle-specific myomiR. Biochim Biophys Acta. 2008; 1779 (11): 682-91. doi: 10.1016/j.bbagrm.2008.03.001 PMID: 18381085
5. Potthoff M J, Olson E N MEF2: a central regulator of diverse developmental programs. Development. 2007; 134(23): 4131-40. PMID: 17959722
6. K Hak K, Lee Yong Sun, Sivaprasad Umasundari, Malhotra Ankit, Dutta Anindya Muscle-specific microRNA miR-206 promotes muscle differentiation. J Cell Biol. 2006; 174 (5): 677-687. PMID: 16923828
7. Anderson Curtis, Catoe Health, Rudolf Werner MIR-206 regulates connexin43 expression during skeletal muscle development. Nucl. Acids Res. 2006; 34(20): 5863-5871. PMID: 17062625
8. Alex S F, Li Nan, T Elizabeth J Zebrafish miR-214 modulates Hedgehog signaling to specify muscle cell fate. Nat Genet. 2007; 39(2): 259-63. PMID: 17220889
9. Zhang Jing, Ying Zheng-zhou, Tang Zhong-lin, Long Liang-qi, Li Kui MicroRNA-148a promotes myogenic differentiation by targeting the ROCK1 gene. The Journal of Biological Chemistry. 2012; 287: 21093-21101. doi: 10.1074/jbc.M111.330381 PMID: 22547064
10. Skonier J, Bennett K, Rothwell V, Kosowski S, Plowman G, Wallace P, et al beta ig-h3: a transforming growth factor-beta-responsive gene encoding a secreted protein that inhibits cell attachment in vitro and suppresses the growth of CHO cells in nude mice. DNA Cell Biol. 1994; 13(6): 571-84. PMID: 8024701
11. F Jill W, M Michelle F Developmental expression patterns of Beta-ig (betaIG-H3) and its function as a cell adhesion protein. Mech Dev.2003; 120(8): 851-64. PMID: 12963107
12. Wen G Y, Hong M, Li B Y, Liao W P, Cheng S K, Hu B R, et al. Transforming growth factor-beta-induced protein (TGFBI) suppresses mesothelioma progression through the Akt/mTOR pathway. Int J Oncol. 2011; 39(4): 1001-9. doi: 10.3892/ijo.2011.1097 PMID: 21701776
13. Tyesha N B, Ronald D C Role of TGF-Bsignaling in inherited and acquired myopathies. BioMed Central. 2011; 1:19
14. Eisenberg I, Eran A, Nishino I, Moggio M, Whitney D, Beggs A H,et al. Distinctive patterns of microRNA expression in primary muscular disorders. Proc Natl Acad Sci. 2007; 104(43): 17016-21. PMID: 17942673
15. Jaime J C, Peter W R Regulation of gene expression in vertebrate skeletal muscle. Exp Cell Res. 2010; 316(18): 3014-8. doi: 10.1016/j.yexcr.2010.07.005 PMID: 20633554
16. Bismuth Keren, Relaix Frederic Genetic regulation of skeletal muscle development. Exp Cell Res. 2010; 316(18): 3081-6. doi: 10.1016/j.yexcr.2010.08.018 PMID: 20828559
17. Hou Xinhua, Tang Zhonglin, Liu Honglin, Wang Ning, Ju Huiming, Li Kui Discovery of MicroRN As Associated with Myogenes is by Deep Sequencing of Serial Developme ntal Skeletal Muscl es in Pigs. Plos One. 2012; 7 (12): 52123.
18. Zhao Shuanping, Zhang Jing, Hou Xinhua, Zan Linsen, Wang Ning, Tang Zhonglin, et al. OLFML3 Expression is Decreased during Prenatal Muscle Development and Regulated by MicroRNA-155 in Pigs. International Journal of Biological Sciences. 2012; 8((4):459-469. doi: 10.7150/ijbs.3821 PMID: 22419891
19. Yang Ya-lan, Li Yan, Liang Ru-Yi, Zhou Rong, Ao Hong, Mou Yu-Lian, et al. Dynamic Expression of MicroRNA-127 During Prenatal and Postnatal Skeletal Muscle Development. Journal of Integrative Agriculture. 2013; doi: 10.1016/S2095-3119(13)60419-0
20. Yin Jie, Bai Zhigang, Song Jianning, Yang Yun, Wang Jin, Han Wei, et al. Differential expression of serum miR-126, miR-141 and miR-21 as novel biomarkers for early detection of liver metastasis in colorectal cancer.Chin J Cancer Res. 2014; 26(1): 95-103. doi: 10.3978/j.issn.1000-9604.2014.02.07 PMID: 24653631
21. Zhang Fang, Yang Zhiping, Cao Minjun, Xu Yinsheng, Li Jintao, Chen Xuebin, et al. MiR-203 suppresses tumor growth and invasion and down-regulates MiR-21 expression through repressing Ran in esophageal cancer.Cancer Lett. 2013; 342(1): 121-129. doi: 10.1016/j.canlet.2013.08.037 PMID: 24001611
22. Zhang Kai-liang, Han Lei, Chen Lu-yue, Shi Zhen-dong, Yang Ming, Ren Yu, et al. Blockage of a miR- 21/EGFR regulatory feedback loop augments anti-EGFR therapy in glioblastomas. Cancer Lett. 2014; 342(1): 139-149. doi: 10.1016/j.canlet.2013.08.043 PMID: 24012640
23. Zhou T B, Jiang Z P Role of miR-21 and its signaling pathways in renal diseases. J Recept Signal Transduct Res. 2014; 34(5):335-7 doi: 10.3109/10799893.2014.896382 PMID: 24576069
24. Wystub Katharina, Besser Johannes, Bachmann Angela, Boettger Thomas, Braun Thomas miR-1/133a clusters cooperatively specify the cardiomyogenic lineage by adjustment of myocardin levels during embryonic heart development PLos Genet. 2013; 9(9): e1003793. doi: 10.1371/journal.pgen.1003793 PMID: 24068960
25. Zhang Duo, Li Xihua, Chen Chuchu, Li Yuyin, Zhao Lei, Jing Yanyan, et al. Attenuation of p38-mediated miR-1/133 expression facilitates myoblast proliferation during the early stage of muscle regeneration. PLos One. 2012; 7(7): e41478 doi: 10.1371/journal.pone.0041478 PMID: 22911796
26. Chen JianFu, Tao Yazhong, Li Juan, Deng Zhongliang, Yan Zhen, Xiao Xiao et al. microRNA-1 and microRNA-206 regulate skeletal muscle satellite cell proliferation and differentiation by repressing Pax7. J Cell Biol. 2010; 190(5): 867-79. doi: 10.1083/jcb.200911036 PMID: 20819939
27. Knezevic Ivana, Patel Aalok, S Nagalinggam R, G Mahesh P, Solaro R John, N Raghu S, et al. A Novel Cardiomyocyte-enriched MicroRNA, miR-378, Targets Insulin-like Growth Factor 1 Receptor implications in postnatal cardiac remodeling and cell survival. Journal of Biological Chemistry. 2012; 287(16): 12913-12926. doi: 10.1074/jbc.M111.331751 PMID: 22367207
28. Ganesan J, Ramanujam D, Sassi Y, Ahles A, Jentzsch C, Werfel S. et al. MiR-378 Controls Cardiac Hypertrophy by Combined Repression of Mitogen-Activated Protein Kinase Pathway Factors. Circulation. 2013; 127(21): 2097-U88. doi: 10.1161/CIRCULATIONAHA.112.000882 PMID: 23625957
29. Blumensatt M, Greulich S, de Wiza D H, Mueller H, Maxhera B, Rabelink M J et al. Activin A impairs insulin action in cardiomyocytes via up-regulation of miR-143. Cardiovasc Res. 2013; 100(2): 201-10. doi: 10.1093/cvr/cvt173 PMID: 23812417
30. Chen L, Wu P, Guo XH, Hu Y, Li YL, Shi J, et al. miR-143: a novel regulator of MyoD expression in fast and slow muscles of Siniperca chuatsi. Curr Mol Med. 2014; 14(3): 370-5. PMID: 24588768
31. Kimberly R C, Neil T S, Mark P W, Emily C B, Sarah U M, Alecia N M, et al. miR-145 and miR-143 regulate smooth muscle cell fate and plasticity. Nature. 2009; 460(7256): 705-10. doi: 10.1038/nature08195 PMID: 19578358
32. Wang Shusheng, A Arin B, J Brett A, Qi Xiaoxia, McAnally John, H Joseph A, et al. The endothelial-specific microRNA miR-126 governs vascular intrgrity and angiogenesis. Dev Cell. 2008; 15:261-271 doi: 10.1016/j.devcel.2008.07.002 PMID: 18694565
33. Ryu Hyun Su, Park Seung-Yoon, Ma Duan, Zhang Jin, Lee Wan The induction of microRNA targeting IRS-1 is involved in the development of insulin resistance under conditions of mitochondrial dysfunction in hepatocytes. Plos One. 2011; 6: e17343 doi: 10.1371/journal.pone.0017343 PMID: 21464990
34. B Tyesha N, C Ronald D Role of TGF-β signaling in inherited and acquired myopathies Burks and Cohn Skeletal Muscle. 2011; 1(19): doi: 10.1186/2044-5040-1-19
35. Cusella D A M G, Molinari S, Le Donne A, Vivarelli E, Bouche Marina, Molinaro M, et al. Differential response of embryonic and fetal myoblasts to TGFβ: a possible regulatory mechanism of skeletal muscle histogenesis. Development. 1994; 120: 925-933. PMID: 7600968
36. Ronald E A, B Linda K Inhibition of skeletal muscle satellite cell differentiation by transforming growth factor-beta. Journal of Cellular Physiology. 1987; 133(3): 567-572. PMID: 3480289
37. Li Yong, Foster William, D Bridget M, Chan Yisheng, Prisk Victor, Tang Ying, et al. Transforming Growth Factor-beta1 Induces the Differentiation of Myogenic Cells into Fibrotic Cells in Injured Skeletal Muscle:A Key Event in Muscle Fibrogenesis. The American Journal of Pathology. 2004; 164(3): 1007-1019. PMID: 14982854
38. Li Tingting, Wu Rimao, Zhang Yong, Zhu Dahai A systematic analysis of the skeletal muscle miRNA transcriptome of chicken varieties with divergent skeletal muscle growth identifies novel miRNAs and differentially expressed miRNAs. BMC Genomics. 2011; 12(186): doi: 10.1186/1471-2164-12-186
39. Sweetman Dylan, Rathjen Tina, Jefferson Matthew, Wheeler Guy, S Terence G, W Grant N., et al. Münsterberg Andrea, Dalmay Tamas, FGF-4 signaling is involved in mir-206 expression in developing somites of chicken embryos. Developmental Dynamics. 2006; 235(8): 2185-2191. PMID: 16804893
40. Gagan Jeffrey, Dey B K, Layer R, Yan Z, Dutta A MicroRNA-378 targets the myogenic repressor MyoR during myoblast differentiation. J Biol Chem. 2011; 286(22): 19431-8. doi: 10.1074/jbc.M111.219006 PMID: 21471220
41. Wanga Li, Chen X, Zheng Y, Li F, Lu Z, Chen C, et al. MiR-23a inhibits myogenic differentiation through down regulation of fast myosin heavy chain isoforms. Exp Cell Res. 2012; 318(18): 2324-34. doi: 10.1016/j.yexcr.2012.06.018 PMID: 22771720
42. Wong Chung Fai, T Ross L MicroRNA-26a Targets the Histone Methyltransferase Enhancer of Zeste homolog 2 during Myogenesis. Journal of Biological Chemistry. 2008; 283: 9836-9843. doi: 10.1074/jbc.M709614200 PMID: 18281287
43. Zhou Liang, Wang Lijun, Lu Leina, Jiang Peiyong, Sun Hao, Huating Wang A novel target of micro-RNA-29, Ring1 and YY1-binding protein (Rybp), negatively regulates skeletal myogenesis. The Journal of Biological Chemistry. 2012; 287: 25255-25265. doi: 10.1074/jbc.M112.357053 PMID: 22661705
44. Grundmann Sebastian, H Felix P, Kinniry Sheena, Heinke Jennifer, Helbing Thomas, Bluhm Franziska H F P, et al. MicroRNA-100 Regulates Neovascularization by Suppression of Mammalian Target of Rapamycin in Endothelial and Vascular Smooth Muscle Cells Circulation. 2011; 123: 999-1009. doi: 10.1161/CIRCULATIONAHA.110.000323 PMID: 21339483
45. Pette Dirk, Staron R S Mammalian Skeletal Muscle Fiber Type Transitions. International Review of Cytology. 1997; 170: 143-223. PMID: 9002237
46. Wigmore P M, Stickland N C Muscle development in large and small pig fetuses. J Anat. 1983; 137(Pt 2): 235-245. PMID: 6630038
47. Tang Zhonglin, Li Yong, Wan Ping, Li Xiaoping, Zhao Shuhong, Liu Bang, et al. LongSAGE analysis of skeletal muscle at three prenatal stages in Tongcheng and Landrace pigs. Genome Biol. 2007; 8(6): R115. PMID: 17573972
48. Hayashi Toru, Koyama Noriko, Azuma Yukio, Masanori Kashimata Mesenchymal miR-21 regulates branching morphogenesis in murine submandibular gland in vitro. Dev Biol. 2011; 352(2): 299-307. doi: 10.1016/j.ydbio.2011.01.030 PMID: 21295561
49. Sarkar J, Gou D, Turaka P, Viktorova E, Ramchandran R, Raj JU, MicroRNA-21 plays a role in hypoxia-mediated pulmonary artery smooth muscle cell proliferation and migration. Am J Physiol Lung Cell Mol Physiol. 2010; 299(6): L861-71. doi: 10.1152/ajplung.00201.2010 PMID: 20693317
50. Chen Po Yu, Manning Heiko, Slanchev Krasimir, Chien Minchen, Russo Jemes J, Ju Jingyue, et al. The developmental miRNA profiles of zebrafish as determined by small RNA cloning. Genes Dev. 2005; 19(11): 1288-93. PMID: 15937218
51. Li Tao Sheng, Komota Takahiro, Ohshima Mako, Qin Shu Lan, Kubo Masayuki, Ueda Kazuhiro, et al. TGF-beta induces the differentiation of bone marrow stem cells into immature cardiomyocytes. Biochem Biophys Res Commun. 2008; 366(4): 1074-80. PMID: 18158919