Sotelo-Silveira José Roberto, Calliari Aldo, Kun Alejandra, Elizondo Victoria, Canclini Lucía, Sotelo José Roberto
Department of Proteins and Nucleic Acids, Instituto de Investigaciones Biológicas Clemente Estable (IIBCE), Av. Italia 3318, CP 11600, Montevideo, Uruguay.
Methods Mol Biol. 2011;714:125-38. doi: 10.1007/978-1-61779-005-8_8.
The conclusive demonstration of RNA in vertebrate axons by in situ hybridization (ISH) has been elusive. We review the most important reasons for difficulties, including low concentration of axonal RNAs, localization in specific cortical domains, and the need to isolate axons. We demonstrate the importance of axon micro-dissection to obtain a whole mount perspective of mRNA distribution in the axonal territory. We describe a protocol to perform fluorescent ISH in isolated axons and guidelines for the preservation of structural and molecular integrity of cortical RNA-containing domains (e.g., Periaxoplasmic Ribosomal Plaques, or PARPs) in isolated axoplasm.
通过原位杂交(ISH)在脊椎动物轴突中确凿证明RNA一直难以实现。我们回顾了造成困难的最重要原因,包括轴突RNA浓度低、在特定皮质区域的定位以及分离轴突的必要性。我们证明了轴突显微切割对于获得轴突区域mRNA分布全貌的重要性。我们描述了一种在分离的轴突中进行荧光ISH的方案,以及在分离的轴浆中保存含皮质RNA区域(如轴周核糖体斑块或PARP)结构和分子完整性的指南。