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The function and application of animal microRNA-181

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  • Key Laboratory of Molecular Cytogenetics and Genetic Breeding of Heilongjiang Province, College of Life Science and Technology, Harbin Normal University, Harbin 150025, China

Received date: 2013-08-22

  Revised date: 2013-12-04

  Online published: 2014-01-20

Abstract

MicroRNAs (miRNAs) are a type of non-coding RNAs which are short (17-25nt) and highly conservative in evolution. They can regulate gene expression by preventing target mRNA translation or inducing degradation via oligonucleotides complementary to target mRNA. Here, we briefly summarize the functions and regulatory mechanisms of microRNA-181 (miR-181) in cell proliferation, apoptosis and differentiation, and discuss the miR-181-mediated regulation of immune response in lymphocyte proliferation and differentiation, autoimmunity, inflammation and virus infection. Also, we analyze the functions of miR-181 in tumorigenesis, tumor development, diagnosis, treatment and prognosis. Finally, we discuss the application prospects of miR-181. The functional studies of miR-181 family members have important significance in understanding the mechanisms of biological events, pathogenesis of diseases, and finding new ways to diagnose and treat related diseases.

Cite this article

Yang Chang, Weitao Mu, Chaolai Man . The function and application of animal microRNA-181[J]. Hereditas(Beijing), 2014 , 36(2) : 103 -110 . DOI: 10.3724/SP.J.1005.2014.0103

References

[1] Huang S, Wu S, Ding J, Lin J, Wei L, Gu J, He X. Mi-croRNA-181a modulates gene expression of zinc finger family members by directly targeting their coding regions. Nucleic Acids Res, 2010, 38(20): 7211–7218. <\p>

[2] Chen CZ, Li L, Lodish HF, Bartel DP. MicroRNAs modu-late hematopoietic lineage differentiation. Science, 2004, 303(5654): 83–86. <\p>

[3] Zhang Q, Sun H, Jiang Y, Ding L, Wu S, Fang T, Yan G, Hu Y. MicroRNA-181a Suppresses Mouse Granulosa Cell Proliferation by Targeting Activin Receptor IIA. PLoS ONE, 2013, 8(3): e59667. <\p>

[4] Liu L, Wang Y, Fan H, Zhao X, Liu D, Hu Y, Kidd AR, Bao J, Hou Y. MicroRNA-181a regulates local immune balance by inhibiting proliferation and immunosuppres-sive properties of mesenchymal stem cells. Stem Cells, 2012, 30(8): 1756–1770. <\p>

[5] Dahlhaus M, Schult C, Lange S, Freund M, Junghanss C. MicroRNA 181a influences the expression of HMGB1 and CD4 in acute Leukemias. Anticancer Res, 2013, 33(2): 445–452. <\p>

[6] Zhu HY, Liu MY, Hong Q, Zhang D, Geng WJ, Xie YS, Chen XM. Role of microRNA-181a in the apoptosis of tubular epithelial cell induced by cisplatin. Chin Med J (Engl), 2012, 125(3): 523–526. <\p>

[7] Chen G, Zhu W, Shi D, Lü L, Zhang C, Liu P, Hu W. Mi-croRNA-181a sensitizes human malignant glioma U87MG cells to radiation by targeting Bcl-2. Oncol Rep, 2010, 23(4): 997–1003. <\p>

[8] Ouyang YB, Lu Y, Yue S, Giffard RG. MiR-181 targets multiple Bcl-2 family members and influences apoptosis and mitochondrial function in astrocytes. Mitochondrion, 2012, 12(2): 213–219. <\p>

[9] Chen H, Chen Q, Fang M, Mi Y. MicroRNA-181b tar-gets MLK2 in HL-60 cells. Sci China Life Sci, 2010, 53(1): 101–106. <\p>

[10] Shi L, Cheng Z, Zhang J, Li R, Zhao P, Fu Z, You Y. Hsa- mir-181a and hsa-mir-181b function as tumor suppressors in human glioma cells. Brain Res, 2008, 1236: 185–193. <\p>

[11] Xu ZY, Jiang JF, Xu C, Wang Y, Sun L, Guo XC, Liu HQ. MicroRNA-181 regulates CARM1 and histone aginine methylation to promote differentiation of human embry-onic stem cells. PLoS ONE, 2013, 8(1): e53146. <\p>

[12] Torres-Padilla ME, Parfitt DE, Kouzarides T, Zernicka- Goetz M. Histone arginine methylation regulates pluripotency in the early mouse embryo. Nature, 2007, 445(7124): 214–218. <\p>

[13] Wu Q, Bruce AW, Jedrusik A, Ellis PD, Andrews RM, Langford CF, Glover DM, Zernicka-Goetz M. CARM1 is required in embryonic stem cells to maintain pluripotency and resist differentiation. Stem Cells, 2009, 27(11): 2637–2645. <\p>

[14] Kane NM, Howard L, Descamps B, Meloni M, McClure J, Lu R, McCahill A, Breen C, Mackenzie RM, Delles C, Mountford JC, Milligan G, Emanueli C, Baker AH. Role of microRNAs 99b, 181a, and 181b in the differentia-tion of human embryonic stem cells to vascular endo-thelial cells. Stem Cells, 2012, 30(4): 643–654. <\p>

[15] O'Loghlen A, Muñoz-Cabello AM, Gaspar-Maia A, Wu HA, Banito A, Kunowska N, Racek T, Pemberton HN, Beolchi P, Lavial F, Masui O, Vermeulen M, Carroll T, Graumann J, Heard E, Dillon N, Azuara V, Snijders AP, Peters G, Bernstein E, Gil J. MicroRNA regulation of Cbx7 mediates a switch of polycomb orthologs during ESC differentiation. Cell Stem Cell, 2012, 10(1): 33–46. <\p>

[16] Mintz PJ, Sætrom P, Reebye V, Lundbæk MB, Lao K, Rossi JJ, Gaensler KM, Kasahara N, Nicholls JP, Jensen S, Haoudi A, Emara MM, Gordon MY, Habib NA. MicroRNA- 181a* targets nanog in a subpopulation of CD34(+) cells isolated from peripheral blood. Mol Ther Nucleic Acids, 2012, 1: e34. <\p>

[17] Niwa H, Toyooka Y, Shimosato D, Strumpf D, Takahashi K, Yagi R, Rossant J. Interaction between Oct3/4 and Cdx2 determines trophectoderm differentiation. Cell, 2005, 123(5): 917–92

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