Zhang Xulun, Zhang Hailing, Oberdick John
Department of Neuroscience and the Neurobiotechnology Center, The Ohio State University, 190 Rightmire Hall, 1060 Carmack Road, Columbus, OH 43210, USA.
Brain Res Mol Brain Res. 2002 Sep 30;105(1-2):1-10. doi: 10.1016/s0169-328x(02)00379-0.
L7/Pcp-2 is a GoLoco domain protein that modulates the activation of Galpha(i) and Galpha(o). We have previously described the Purkinje cell-specific expression of the Pcp-2(L7) gene and the abundant localization of its mRNA in mouse cerebellar Purkinje cell dendrites. Here we report on two alternative cerebellar forms of the L7/Pcp-2 mRNA and protein by examination of the gene structures and cDNA sequences of the mouse, rat, and human genes. The structures of the rodent and human genes are very similar with the most notable difference in the genomic configuration of the first exon. Despite this difference, the human and rodent genes both encode two alternative mRNAs due to the choice of two transcriptional start positions. The two mRNA forms, in turn, predict two forms of the L7/Pcp-2 protein, which are both highly conserved across species. These two protein forms differ with respect to the number of GoLoco domains. Lastly we examined the issue of mRNA localization in dendrites. In mouse both mRNA forms are detectable in dendrites but their relative proportions change during development. In addition we performed in situ hybridization on a developmental series of human cerebellar sections and demonstrate that the L7/Pcp-2 mRNA is also localized in dendrites of humans. As previously described in the mouse the dendritic localization in humans is developmentally regulated being most prominent during the peak phase of synaptogenesis and decreasing dramatically with age. The conservation of all of these properties of both the L7/Pcp-2 protein and mRNA highlights their likely importance in controlling the development and/or motor control function of Purkinje cells.
L7/Pcp-2是一种具有GoLoco结构域的蛋白质,可调节Gα(i)和Gα(o)的激活。我们之前曾描述过Pcp-2(L7)基因在浦肯野细胞中的特异性表达及其mRNA在小鼠小脑浦肯野细胞树突中的大量定位。在此,我们通过对小鼠、大鼠和人类基因的基因结构和cDNA序列进行研究,报告了L7/Pcp-2 mRNA和蛋白质的两种小脑特异形式。啮齿动物和人类基因的结构非常相似,最显著的差异在于第一个外显子的基因组构型。尽管存在这种差异,但由于选择了两个转录起始位置,人类和啮齿动物基因均编码两种可变mRNA。这两种mRNA形式进而预测了L7/Pcp-2蛋白质的两种形式,它们在物种间都高度保守。这两种蛋白质形式在GoLoco结构域的数量上有所不同。最后,我们研究了mRNA在树突中的定位问题。在小鼠中,两种mRNA形式在树突中均可检测到,但它们的相对比例在发育过程中会发生变化。此外,我们对人类小脑切片的发育系列进行了原位杂交,并证明L7/Pcp-2 mRNA也定位于人类的树突中。正如之前在小鼠中所描述的那样,人类树突中的定位在发育过程中受到调控,在突触发生的高峰期最为突出,并随着年龄的增长而显著下降。L7/Pcp-2蛋白质和mRNA的所有这些特性的保守性突出了它们在控制浦肯野细胞发育和/或运动控制功能方面可能的重要性。