Guiffre A, Atkinson K, Kearney P
Department of Hematology, St. Vincent's Hospital, Rushcutter's Bay, Australia.
Anal Biochem. 1993 Jul;212(1):50-7. doi: 10.1006/abio.1993.1290.
The quantitation of low abundance messenger (m)RNA species such as that for interleukin 5 (IL-5) cannot be achieved by Northern blotting. Polymerase chain reaction (PCR) technology can be used to overcome this paucity of target molecules, but in its standard format it is semiquantitative. We describe the synthesis, purification, and use of a synthetic IL-5 mRNA (cRNA) molecule which, when included in the PCR reaction, enabled the amplification of IL-5 mRNA molecules from clinical samples to be made quantitative. A stringent protocol involving analysis of the purified transcript by PCR (to ensure its freedom from template molecules) is required. Preliminary experiments indicate that IL-5 mRNA levels are elevated in asthmatics.
低丰度信使核糖核酸(mRNA)种类(如白细胞介素5(IL-5)的mRNA)的定量无法通过Northern印迹法实现。聚合酶链反应(PCR)技术可用于克服靶分子数量不足的问题,但其标准形式是半定量的。我们描述了一种合成的IL-5 mRNA(cRNA)分子的合成、纯化及应用,当将其加入PCR反应时,可使从临床样本中扩增的IL-5 mRNA分子实现定量。需要一个严格的方案,包括通过PCR分析纯化的转录本(以确保其不含模板分子)。初步实验表明,哮喘患者的IL-5 mRNA水平升高。