Frantz G D, Wuenschell C W, Messer A, Tobin A J
Department of Biology, University of California, Los Angeles, USA.
J Neurosci Res. 1996 May 1;44(3):255-62. doi: 10.1002/(SICI)1097-4547(19960501)44:3<255::AID-JNR6>3.0.CO;2-F.
We used in situ hybridization to study the expression of GAD67 and calbindin D28K mRNAs in developing mouse cerebellar Purkinje cells. Both genes are expressed prenatally; calbindin D28K mRNAs can be detected in Purkinje cells of embryonic day (E) 15 mice, whereas GAD67 mRNAs first appear slightly later, in E16 mice. The stunted Purkinje cells of staggerer (sg/sg) mutant mice maintain calbindin D28K and GAD67 expression. Our data suggest that the sg/sg mutation does not interfere with the transcriptional activation of these two genes, and might therefore act after the induction of specific gene expression in developing Purkinje cells.
我们采用原位杂交技术研究了发育中小鼠小脑浦肯野细胞中GAD67和钙结合蛋白D28K mRNA的表达。这两个基因在出生前均有表达;在胚胎第15天(E15)小鼠的浦肯野细胞中可检测到钙结合蛋白D28K mRNA,而GAD67 mRNA首次出现稍晚,在E16小鼠中出现。蹒跚(sg/sg)突变小鼠发育不良的浦肯野细胞维持钙结合蛋白D28K和GAD67的表达。我们的数据表明,sg/sg突变并不干扰这两个基因的转录激活,因此可能在发育中的浦肯野细胞中特定基因表达诱导之后发挥作用。