Sashihara S, Felts P A, Waxman S G, Matsui T
Department of Neurology, Yale University School of Medicine, New Haven, CT 06520-8018, USA.
Brain Res Mol Brain Res. 1996 Nov;42(1):109-17. doi: 10.1016/s0169-328x(96)00118-0.
We analyzed expression of mouse orphan nuclear receptor ROR alpha during postnatal development of rodent brain. Using a riboprobe corresponding to the 3'-end of mROR alpha cDNA a peak of ROR alpha expression was observed at postnatal 16 day (P16) in the Purkinje cells of cerebellum, neurons of the thalamus and the olfactory bulb. The hippocampus was also shown to express ROR alpha with an earlier peak at P7. Expression in cell types other than the Purkinje cells appeared transient. On the other hand, when a probe to the 5'-end of mROR alpha cDNA was used, we observed patterns of ROR alpha expression that are different from those observed with the 3'-probe. No specific transcripts of ROR alpha were detected with the 5'-probe in the Purkinje cells until P16. Additionally, the relative level of the hybridization signals with the 5'-probe and the 3'-probe were different among the various brain regions. Together with the previous findings that ROR alpha comprises at least four isoforms which differ from one another in their N-terminal regions, these observations suggest that the spatiotemporal expression of ROR alpha is under isoform-specific regulation. The timing of its expression suggests that ROR alpha may be involved in regulation of postnatal maturation of specific classes of neurons.
我们分析了啮齿动物脑产后发育过程中小鼠孤儿核受体RORα的表达情况。使用与mRORα cDNA 3'端对应的核糖探针,在出生后第16天(P16),在小脑的浦肯野细胞、丘脑神经元和嗅球中观察到RORα表达的峰值。海马体也显示出表达RORα,在P7时出现较早的峰值。除浦肯野细胞外,其他细胞类型中的表达似乎是短暂的。另一方面,当使用针对mRORα cDNA 5'端的探针时,我们观察到的RORα表达模式与使用3'探针时观察到的不同。直到P16,在浦肯野细胞中用5'探针未检测到RORα的特异性转录本。此外,在不同脑区中,5'探针和3'探针的杂交信号相对水平不同。结合之前的研究结果,即RORα至少包含四种在N端区域彼此不同的亚型,这些观察结果表明RORα的时空表达受亚型特异性调控。其表达时间表明RORα可能参与特定类型神经元产后成熟的调控。