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Establishment of miR-106b Transgenic Mouse |
WANG Hai-lin, QUAN Xiong-zhi, DONG Wei, ZONG Yuan-yuan, LIU Jia-lin, QIN Chuan |
Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences, Key Laboratory of Human Disease Animal Model, State Administration of Tranditional Chinese Medicine, Beijing 100021, China |
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Abstract Objective:To establish a miR-106b transgenic mouse and investigate its effect on the development of Alzheimer’s disease (AD). Methods:The expression vector of miR -106b was constructed. The transgenic mouse was produced by microinjection and genotype was detected by PCR. The expression levels of miR-106b were detected by real time RT-PCR. The protein levels of TGFBR2 were detected by Western blot. Results:Five founders of miR-106b transgenic mice were established and one high-level expression line was identified. Compared with the wild type mice, the expression of TGFBR2 was increased in miR-106b transgenic mice. Conclusion:miR-106b transgenic mouse has been established and it can be used to investigate the function of miR-106b on the development of Alzheimer’s disease.
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Received: 26 August 2010
Published: 25 December 2010
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[1] |
Hébert S S, Horré K, Nicola L, et al. MicroRNA regulation of Alzheimer’s amyloid precursor protein expression. Neurobiol Dis, 2009, 33(3):422-428.
|
|
|
[2] |
王海林,刘嘉琳,宗园媛,等. Mir-106b对阿尔茨海默病昼夜节律调控的初步研究.中国比较医学杂志,2010,20(4):19-23. Wang H L, Liu J L, Zong Y Y, et al. Chinese Journal of Comparative Medicine, 2010, 20(4): 19-23.
|
|
|
[3] |
王晓映,宗园媛,张连峰,等. 阿尔茨海默病中mir-222作用机制的初步研究.中国比较医学杂志,2008,18(9):13-15. Wang X Y, Zong Y Y, Zhang L F, et al. Chinese Journal of Comparative Medicine, 2008, 18(9): 13-15.
|
|
|
[4] |
Wang H, Liu J, Zong Y, et al. miR-106b aberrantly expressed in a double transgenic mouse model for Alzheimer’s disease targets TGF-β type II receptor. Brain Res, 2010, 1357: 166-174.
|
|
|
[5] |
Vasudevan S, Tong Y, Steitz J A. Switching from repression to activation: microRNAs can up-regulate translation. Science, 2007, 318(5858):1931-1934.
|
|
|
[6] |
Hobert O. miRNAs play a tune. Cell,2007, 131(1):22-24.
|
|
|
[7] |
Karres J S, Hilgers V, Carrera I, et al.The conserved microRNA miR-8 tunes atrophin levels to prevent neurodegeneration in Drosophila. Cell, 2007, 131(1):136-145.
|
|
|
[8] |
Ambs S, Prueitt R L, Yi M, et al. Genomic profiling of microRNA and messenger RNA reveals deregulated microRNA expression in prostate cancer. Cancer Res, 2008, 68(15):6162-6170.
|
|
|
[9] |
Pichiorri F, Suh S S, Ladetto M, et al. MicroRNAs regulate critical genes associated with multiple myeloma pathogenesis. Proc Natl Acad Sci U S A, 2008, 105(35):12885-12890.
|
|
|
[10] |
Kim Y K, Yu J, Han T S, et al. Functional links between clustered microRNAs: suppression of cell-cycle inhibitors by microRNA clusters in gastric cancer. Nucleic Acids Res, 2009, 37(5):1672-1681.
|
|
|
[11] |
Ivanovska I, Ball A S, Diaz R L, et al. MicroRNAs in the miR-106b family regulate p21/CDKN1A and promote cell cycle progression. Mol Cell Biol, 2008, 28(7):2167-2174.
|
|
|
[12] |
Petrocca F, Visone R, Onelli M R, et al. E2F1-regulated microRNAs impair TGFbeta-dependent cell-cycle arrest and apoptosis in gastric cancer. Cancer Cell, 2008, 13(3):272-286.
|
|
|
[13] |
Petrocca F, Vecchione A, Croce C M. Emerging role of miR-106b-25/miR-17-92 clusters in the control of transforming growth factor beta signaling. Cancer Res, 2008, 68(20):8191-8194.
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