Lewis M E, Krause R G, Roberts-Lewis J M
Cephalon, Inc., West Chester, Pennsylvania 19380.
Synapse. 1988;2(3):308-16. doi: 10.1002/syn.890020321.
Synthetic oligonucleotides have been used with increasing frequency as probes for the detection and study of the regulation of specific mRNAs by in situ hybridization histochemistry. These probes can be easily obtained and used by the nonmolecular biologist, and they have been shown to be effective for the study of a wide range of mRNAs in neuronal and neuroendocrine tissues. Considerations in oligonucleotide probe design, synthesis, purification, and labeling are described in this article, and current procedures for tissue preparation and hybridization are discussed. In addition, control procedures and methods for the quantitation of in situ hybridization by image analysis are discussed. Finally, the combination of this technique with immunocytochemistry and retrograde tract-tracing is reviewed. The coupling of quantitative in situ hybridization with other neuronal markers, e.g., of connectivity, provides an increasingly valuable technology for exploring the regulation of gene expression in a rich anatomical context.
合成寡核苷酸作为原位杂交组织化学检测和研究特定mRNA调控的探针,其使用频率越来越高。这些探针非分子生物学家也能轻松获取和使用,并且已证明它们对研究神经元和神经内分泌组织中的多种mRNA有效。本文描述了寡核苷酸探针设计、合成、纯化和标记的注意事项,并讨论了当前的组织制备和杂交程序。此外,还讨论了对照程序以及通过图像分析对原位杂交进行定量的方法。最后,综述了该技术与免疫细胞化学和逆行束路追踪的结合。定量原位杂交与其他神经元标记物(如连接性标记物)的结合,为在丰富的解剖背景下探索基因表达调控提供了一项越来越有价值的技术。