Paul M, Wagner D, Metzger R, Ganten D, Lang R E, Suzuki F, Murakami K, Burbach J H, Ludwig G
German Institute for High Blood Pressure Research, Heidelberg, FRG.
J Hypertens. 1988 Mar;6(3):247-52. doi: 10.1097/00004872-198803000-00010.
A new solution hybridization assay was established for the measurement of renin mRNA. The assay makes use of a radioactively labelled renin complementary RNA as hybridization probe and allows rapid and sensitive detection of renin mRNA in amounts as low as 0.5 pg. With this assay it was possible to quantify renin mRNA in tissues with low-gene expression such as brain and heart as well as in testis, kidney and the submandibular gland (SMG) of mice. The concentrations in these organs were 0.03, 0.07, 1, 5.2 and 164 pg renin mRNA/micrograms RNA, respectively. These results are in agreement with Northern blotting experiments. The general applicability and ease of the solution hybridization assay described here should greatly improve the rapidity of mRNA measurements in future functional studies.
建立了一种用于测量肾素mRNA的新型溶液杂交测定法。该测定法使用放射性标记的肾素互补RNA作为杂交探针,能够快速、灵敏地检测低至0.5 pg的肾素mRNA。通过该测定法,可以对基因表达水平较低的组织(如脑和心脏)以及小鼠的睾丸、肾脏和下颌下腺(SMG)中的肾素mRNA进行定量。这些器官中的浓度分别为0.03、0.07、1、5.2和164 pg肾素mRNA/微克RNA。这些结果与Northern印迹实验结果一致。本文所述溶液杂交测定法的普遍适用性和简便性应能极大地提高未来功能研究中mRNA测量的速度。