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Glial cell-line derived neurotrophic factor and neurturin regulate the expressions of distinct miRNA precursors through the activation of GFRα2
被引:10
作者:
Yoong, Li Foong
Wan, Guoqiang
Too, Heng-Phon
机构:
[1] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Singapore 117597, Singapore
[2] Singapore Massachusetts Inst Technol Alliance, MEBCS, Singapore, Singapore
[3] Johns Hopkins Singapore, Biopolis, Singapore, Singapore
关键词:
GDNF family receptor alpha-2;
glial cell line-derived neurotrophic factor;
microRNA;
neurturin;
receptor tyrosine kinase Ret;
D O I:
10.1111/j.1471-4159.2006.03959.x
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Glial cell line-derived neurotrophic factor (GDNF) and neurturin (NTN) are structurally related neurotrophic factors that have both been shown to prevent the degeneration of dopaminergic neurons in vitro and in vivo. NTN and GDNF are thought to bind with different affinities to the GDNF family receptor alpha-2 (GFR alpha 2), and can activate the same multi-component receptor system consisting of GFR alpha 2, receptor tyrosine kinase Ret (RET) and NCAM. MicroRNAs (miRNAs) are a class of short, non-coding RNAs that regulate gene expression through translational repression or RNA degradation. miRNAs have diverse functions, including regulating differentiation, proliferation and apoptosis in several organisms. It is currently unknown whether GDNF and NTN regulate the expression of miRNAs through activation of the same multi-component receptor system. Using quantitative real-time PCR, we measured the expression of some miRNA precursors in human BE(2)-C cells that express GFR alpha 2 but not GFR alpha 1. GDNF and NTN differentially regulate the expression of distinct miRNA precursors through the activation of mitogen-activated protein kinase (extracellular signal-regulated kinase 1/2). This study showed that the expression of distinct miRNA precursors is differentially regulated by specific ligands through the activation of GFR alpha 2.
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页码:1149 / 1158
页数:10
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