Saint-Jeannet Jean-Pierre
Department of Basic Science and Craniofacial Biology, College of Dentistry, New York University, New York, New York 10010
Cold Spring Harb Protoc. 2017 Dec 1;2017(12):pdb.prot097287. doi: 10.1101/pdb.prot097287.
Historically, techniques to analyze the localized distribution of mRNAs during development were performed on sectioned embryos using radioactively labeled riboprobes. The processing of the tissues and the use of emulsion autoradiography were laborious and time-consuming, leading to the development of more direct approaches. The nonradioactive whole-mount in situ hybridization method was first introduced in embryos, and later adapted to embryos for abundant transcripts such as muscle actin. Since then, the technique has been improved and is now broadly used for the spatial detection of even less abundant transcripts in The technique has been especially powerful in the analysis of changes in gene expression in embryos manipulated by mRNA or antisense oligonucleotides microinjection, and in animal cap explants exposed to exogenous factors. The protocol described here provides an excellent signal-to-noise ratio for most labeled probes. It also is relatively high-throughput: With a little practice, approximately 50 samples can easily be processed simultaneously.
从历史上看,在发育过程中分析mRNA局部分布的技术是通过使用放射性标记的核糖探针在切片胚胎上进行的。组织处理和乳胶放射自显影的使用既费力又耗时,这促使了更直接方法的发展。非放射性全胚胎原位杂交方法于1989年首次在斑马鱼胚胎中引入,后来适用于非洲爪蟾胚胎以检测肌肉肌动蛋白等丰富转录本。从那时起,该技术不断改进,现在广泛用于检测非洲爪蟾中甚至丰度更低的转录本的空间分布。该技术在分析通过mRNA或反义寡核苷酸显微注射操作的胚胎以及暴露于外源因子的动物帽外植体中的基因表达变化方面特别有效。这里描述的方案对于大多数标记探针都提供了出色的信噪比。它也是相对高通量的:稍加练习,大约50个样本可以轻松地同时处理。