Denny P, Hamid Q, Krause J E, Polak J M, Legon S
Department of Histochemistry and Chemical Pathology, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.
Histochemistry. 1988;89(5):481-3. doi: 10.1007/BF00492605.
In situ hybridisation detection of mRNAs using riboprobes has become a widely used technique. However, the identification of cells producing closely-related yet distinct mRNAs is difficult with the usual size probes. Moreover, it is not always easy to obtain the required cDNA essential for cRNA probe synthesis. To avoid these problems, we have used synthetic oligodeoxynucleotides to generate short, single stranded RNA probes ("oligo-riboprobes"). These probes can be labelled to very high (10(9) cpm/micrograms) specific activity and can be prepared for any published nucleotide sequence. We have used these probes to localise beta (preprotachykinin) PPT mRNA producing neurons in rat hypothalamus and bowel. The results were compared to that obtained with cRNA probes generated from beta preprotachykinin cDNA.
使用核糖核酸探针进行mRNA的原位杂交检测已成为一种广泛应用的技术。然而,使用常规大小的探针难以鉴定产生密切相关但又不同的mRNA的细胞。此外,要获得cRNA探针合成所必需的所需cDNA并非总是容易的。为避免这些问题,我们使用合成寡脱氧核苷酸来生成短的单链RNA探针(“寡核糖核酸探针”)。这些探针可以标记到非常高的(10⁹ cpm/μg)比活性,并且可以针对任何已发表的核苷酸序列进行制备。我们已使用这些探针来定位大鼠下丘脑和肠道中产生β(前速激肽原)PPT mRNA的神经元。将结果与从β前速激肽原cDNA产生的cRNA探针所获得的结果进行了比较。