Guo H, Sekiguchi M, Tanaka O, Inoue T, Shima H, Nagao M, Tamura S, Abe H
Department of Morphology, Tokai University School of Medicine, Isehara, Japan.
Brain Res Mol Brain Res. 1995 Oct;33(1):121-6. doi: 10.1016/0169-328x(95)00121-8.
We used in situ hybridization to search for the expression of three protein phosphatase (PP) mRNAs in Purkinje cells of normal mice, and staggerer (sg/sg) and reeler (rl/rl) mutant mice, two strains with known Purkinje cell disorders. The expression of the mRNAs was comparable in the normal and rl/rl Purkinje cells, but considerably reduced in the sg/sg. We interpret this finding as indicating: (a) the staggerer mutant gene may directly affect the phosphatase component of the protein phosphorylation-dephosphorylation cycle in the sg/sg Purkinje cells; or (b) the reduced mRNA expression may be a secondary phenomenon, resulting from abnormal Purkinje cell function due to the lack of synaptic input.
我们运用原位杂交技术,探寻三种蛋白磷酸酶(PP)mRNA在正常小鼠、蹒跚突变小鼠(sg/sg)和旋转突变小鼠(rl/rl)浦肯野细胞中的表达情况,后两种是已知存在浦肯野细胞功能紊乱的品系。正常小鼠和rl/rl小鼠的浦肯野细胞中mRNA的表达相当,但在sg/sg小鼠中显著降低。我们将这一发现解释为表明:(a)蹒跚突变基因可能直接影响sg/sg小鼠浦肯野细胞中蛋白质磷酸化-去磷酸化循环的磷酸酶成分;或者(b)mRNA表达降低可能是一种继发现象,是由于缺乏突触输入导致浦肯野细胞功能异常所致。