生物素化寡核苷酸探针在垂体激素mRNA检测中的应用:northern blot分析、光镜和电镜原位杂交。

The Histochemical Journal Pub Date : 1994-10-01
A Matsuno, A Teramoto, S Takekoshi, H Utsunomiya, Y Ohsugi, S Kishikawa, R Y Osamura, T Kirino, R V Lloyd
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引用次数: 0

摘要

放射性同位素原位杂交(ISH)研究证实了正常垂体和垂体腺瘤中垂体激素mrna的存在,已有许多报道。最近的研究表明,与放射性同位素方法相比,非放射性同位素ISH具有几个优点。使用ISH和生物素化寡核苷酸探针,我们已经能够在大鼠正常垂体和人垂体腺瘤的石蜡或冷冻切片中定位各种垂体激素mrna。在对照研究中,我们使用带传感探针的ISH、不带探针的ISH、核糖核酸酶预处理的ISH、带β -肌动蛋白探针的ISH和Northern blot杂交。采用生物素化探针,Northern blot杂交检测大鼠生长激素和催乳素基因转录本。同样的生物素化探针不仅用于光镜下的ISH,还用于电镜下粗内质网多体上大鼠生长激素和催乳素mrna的显示。强调生物素化寡核苷酸探针适用于三种杂交方法,即Northern blot杂交和ISH杂交,在光镜和电镜水平上可用于垂体内分泌功能的分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Application of biotinylated oligonucleotide probes to the detection of pituitary hormone mRNA using northern blot analysis, in situ hybridization at the light- and electron-microscope levels.

There have been many reports on radioisotopic in situ hybridization (ISH) studies for the demonstration of pituitary hormone mRNAs in normal pituitary gland and pituitary adenomas. Recent studies have revealed that non-radioisotopic ISH has several advantages over the radioisotopic method. Using ISH with biotinylated oligonucleotide probes, we have been able to localize various pituitary hormone mRNAs in paraffin wax or frozen sections of rat normal pituitary gland and human pituitary adenomas. For control studies we used ISH with sense probes, ISH without probes, pretreatment with ribonuclease, ISH with a probe for beta-actin and Northern blot hybridization. Using biotinylated probes, gene transcripts of rat growth hormone and prolactin were detected by Northern blot hybridization. The same biotinylated probes were used not for light microscope ISH but also for the electron microscopical demonstration of rat growth hormone and prolactin mRNAs on the polysomes of the rough endoplasmic reticula. It is emphasized that biotinylated oligonucleotide probes are useful for the analysis of pituitary endocrine function because they are applicable to the three hybridization methods, namely, Northern blot hybridization and ISH at the light and electron microscope levels.

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