Sugiura Y, Mori N
Division of Neurogerontology, Ethel Percy Andrus Gerontology Center, University of Southern California, Los Angeles 90089, USA.
Brain Res Dev Brain Res. 1995 Dec 21;90(1-2):73-91. doi: 10.1016/0165-3806(96)83488-2.
The gene encoding SCG10 was originally isolated as a neuronal marker from neural crest derivatives, implying that this protein may contribute to fundamental neuronal properties. To examine the developmental change of SCG10 expression in brain, immunoblot analysis and in situ hybridization were performed in embryonic day 15 (E15), E19, postnatal day 0 (P0), P6, P14, P30 and P90 rat brains. The distribution of SCG10 mRNA was compared to those of its homologue, p19/stathmin, and the well-characterized growth-associated protein GAP-43. Overall expression of SCG10 in brain reached a peak at E19 and decreased gradually by P30 to the adult level. The expression pattern of SCG10 in E15 whole body was identical with that of GAP-43; both mRNAs were specifically detected in developing neuronal structures. p19/stathmin mRNA, on the other hand, showed widespread expression throughout the whole body. Expression patterns of the three mRNAs overlapped in many structures in the perinatal brain, yet each showed unique expression during postnatal development. For example, in the developing cerebellum, strong GAP-43 expression was found in the external granule cells, which are presumably extending parallel fibers, while SCG10 strongly hybridized in the internal granule cells which have reached their final position and begun dendrite outgrowth. The unique transient expression of p19/stathmin was found in the subventricular zone in the cortex, the white matter in the cerebellum, the optic nerve layer of the superior colliculus and the inner edge of the dentate granule layer in the hippocampus. Considering the timing, all of these areas are known to produce neurons or glia. This is consistent with the suggestion that p19/stathmin is related to differentiation. SCG10 may be a new member of growth-associated proteins and this protein may contribute to neurite extension in perinatal brain as does GAP-43. However, the differential expression between SCG10 and GAP-43 in later developmental stages suggests their diverse functions, which indicates these proteins may play different roles during postnatal brain development.
编码SCG10的基因最初是作为一种神经嵴衍生物的神经元标记物分离出来的,这意味着这种蛋白质可能对基本的神经元特性有贡献。为了研究大脑中SCG10表达的发育变化,在胚胎第15天(E15)、E19、出生后第0天(P0)、P6、P14、P30和P90的大鼠大脑中进行了免疫印迹分析和原位杂交。将SCG10 mRNA的分布与其同源物p19/Stathmin以及特征明确的生长相关蛋白GAP-43的分布进行了比较。大脑中SCG10的总体表达在E19达到峰值,并在P30时逐渐下降至成年水平。E15全身中SCG10的表达模式与GAP-43相同;两种mRNA都在发育中的神经元结构中被特异性检测到。另一方面,p19/Stathmin mRNA在全身广泛表达。三种mRNA的表达模式在围产期大脑的许多结构中重叠,但每种在出生后发育过程中都表现出独特的表达。例如,在发育中的小脑中,在可能正在延伸平行纤维的外颗粒细胞中发现了强烈的GAP-43表达,而SCG10在已到达其最终位置并开始树突生长的内颗粒细胞中强烈杂交。在皮质的脑室下区、小脑的白质、上丘的视神经层和海马齿状颗粒层的内边缘发现了p19/Stathmin独特而短暂的表达。考虑到时间,所有这些区域都已知会产生神经元或神经胶质细胞。这与p19/Stathmin与分化相关的观点一致。SCG10可能是生长相关蛋白的一个新成员,并且这种蛋白质可能像GAP-43一样在围产期大脑中促进神经突延伸。然而,SCG10和GAP-43在后期发育阶段的差异表达表明它们具有不同的功能,这表明这些蛋白质在出生后大脑发育过程中可能发挥不同的作用。