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首页> 外文期刊>Journal of Neuroscience Research >Expression and regulation of the LIM-class homeobox gene rlim-1 in neuronal progenitors of the rat cerebellum.
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Expression and regulation of the LIM-class homeobox gene rlim-1 in neuronal progenitors of the rat cerebellum.

机译:LIM类同源盒基因rlim-1在大鼠小脑神经元祖细胞中的表达和调控。

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To investigate LIM gene function in the rat cerebellar system, we analyzed expression and regulation of the rat homologue of frog Xlim-1 (rlim-1) in vivo and in cultured cells. In developing cerebellum, peak levels of rlim-1 mRNA at postnatal day 8 (p8) are coincident with the peak period of granule cell proliferation. Analysis of rlim-1 protein with a specific antibody showed that expression was also maximal at p8. In situ hybridization showed that at p8 rlim-1 mRNA was expressed in Purkinje and granule cells. Both the proliferative and the premigratory granule cells in the external germinal zone displayed high levels of rlim-1 mRNA expression. Immunocytochemical staining demonstrated that at p8 rlim-1 protein was also present in proliferative and premigratory granule cells. In adult cerebellum (p30), rlim-1 mRNA and protein expression in granule cells was strongly attenuated. The down-regulation of rlim-1 mRNA occurred in granule cells just after the time of final division, coinciding with the onset of their migration. rlim-1 protein was detected in migratory granule neurons. The developmental decrease in rlim-1 mRNA and protein found in vivo was reproduced in pure cerebellar granule cell cultures. In these cultures, granule neurons were postmitotic 1 day after plating but still displayed high levels of rlim-1 protein expression up to 3 days in vitro. Our findings indicate that 1) rlim-1 is likely to act in concert with other genes to specify granule cell fate, 2) rlim-1 expression in granule neurons is regulated autonomously, and 3) rlim-1 protein may also play an important role in granule neuron differentiation and survival. Published 2001 Wiley-Liss, Inc.
机译:为了研究LIM基因在大鼠小脑系统中的功能,我们分析了青蛙Xlim-1(rli​​m-1)在体内和培养细胞中大鼠同源物的表达和调控。在发育中的小脑中,出生后第8天(p8)的rlim-1 mRNA峰值水平与颗粒细胞增殖的高峰期一致。用特异抗体分析rlim-1蛋白显示,在p8处表达也最大。原位杂交表明在p8 rlim-1 mRNA在Purkinje和颗粒细胞中表达。外部生发区的增殖和迁移前颗粒细胞均显示高水平的rlim-1 mRNA表达。免疫细胞化学染色表明在p8 rlim-1蛋白也存在于增殖和迁移前的颗粒细胞中。在成年小脑(p30)中,颗粒细胞中rlim-1 mRNA和蛋白表达强烈减弱。 rlim-1 mRNA的下调恰好在最终分裂后立即在颗粒细胞中发生,这与它们的迁移开始相吻合。在迁徙的颗粒神经元中检测到rlim-1蛋白。体内发现的rlim-1 mRNA和蛋白质的发育下降在纯小脑颗粒细胞培养物中得以再现。在这些培养物中,铺板后1天颗粒神经元发生有丝分裂,但直到体外培养3天仍显示高水平的rlim-1蛋白表达。我们的发现表明:1)rlim-1可能与其他基因协同作用以指定颗粒细胞的命运,2)rlim-1在颗粒神经元中的表达是自主调节的,并且3)rlim-1蛋白也可能起重要作用在颗粒神经元的分化和存活。 2001年出版的Wiley-Liss,Inc.

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