Litman P, Barg J, Ginzburg I
Department of Neurobiology, Weizmann Institute of Science, Rehovot, Israel.
Neuron. 1994 Dec;13(6):1463-74. doi: 10.1016/0896-6273(94)90432-4.
Subcellular localization of neuronal mRNAs contributes to the development of identifiable microdomains. In differentiated neurons, tau mRNA is localized in the cell body and the proximal portion of the axon, and MAP2 mRNA is localized in the cell body and dendrites, whereas tubulin mRNA is restricted to the cell body. To investigate the mechanism(s) leading to segregation of mictrotubule-associated protein mRNA, we examined the role of the cytoskeleton in this process. Detergent extraction of primary neuronal cells in culture followed by in situ hybridization analysis demonstrated that tau mRNA remains bound to cytoskeleton of the treated cells. In addition, biochemical fractionation showed that tau and MAP2 mRNAs are preferentially associated with the fraction of assembled microtubules. In contrast, mRNAs restricted to the neuronal cell body, such as those of tubulin, the 68 kDa neurofilament, and mouse GAPDH, are preferentially found in the supernatant. Using cytoskeletal inhibitors, we demonstrate that tau mRNA is associated with the microtubule system, and not with the actin filaments, thus supporting the hypothesis that the mechanism of mRNA localization is a multistep pathway in which the microtubules play a crucial role.
神经元mRNA的亚细胞定位有助于可识别的微结构域的形成。在分化的神经元中,tau mRNA定位于细胞体和轴突近端,MAP2 mRNA定位于细胞体和树突,而微管蛋白mRNA则局限于细胞体。为了研究导致微管相关蛋白mRNA分离的机制,我们研究了细胞骨架在这一过程中的作用。用去污剂提取培养的原代神经元细胞,然后进行原位杂交分析,结果表明tau mRNA仍与处理过的细胞的细胞骨架结合。此外,生化分级分离显示tau和MAP2 mRNA优先与组装好的微管部分相关。相比之下,局限于神经元细胞体的mRNA,如微管蛋白、68 kDa神经丝和小鼠甘油醛-3-磷酸脱氢酶的mRNA,则优先存在于上清液中。使用细胞骨架抑制剂,我们证明tau mRNA与微管系统相关,而不与肌动蛋白丝相关,从而支持了mRNA定位机制是一个多步骤途径的假说,其中微管起着关键作用。