Siebert P D, Larrick J W
CLONTECH Laboratories, Palo Alto, CA 94303-4607.
Biotechniques. 1993 Feb;14(2):244-9.
A rapid and reliable method is described for preparing competitive DNA fragments for quantitative PCR. Synthetic DNAs complementary to previously established PCR primers are ligated together with the primers to both ends of a generic DNA fragment whose length differs from the natural target gene PCR product. After a short ligation step, the properly constructed ligation products (i.e., those that have the correct primer templates on opposite sides of the generic DNA fragment) are preferentially amplified by PCR. The generation of competitive PCR fragments, MIMICS, can be completed in a single day. To perform quantitative PCR, known quantities of PCR MIMICS are spiked into PCR amplification reactions containing the experimental cDNA samples. A visual or radioactive comparison of the PCR products can then be used to determine the initial quantity of target gene. We show that competitive PCR MIMICS can be used to accurately measure small changes in mRNA levels.
本文描述了一种快速可靠的方法,用于制备用于定量PCR的竞争性DNA片段。与先前建立的PCR引物互补的合成DNA与引物连接到一个通用DNA片段的两端,该通用DNA片段的长度与天然靶基因PCR产物不同。经过短暂的连接步骤后,正确构建的连接产物(即在通用DNA片段相对两侧具有正确引物模板的产物)通过PCR优先扩增。竞争性PCR片段(MIMICS)的生成可在一天内完成。为了进行定量PCR,将已知量的PCR MIMICS加入到含有实验cDNA样品的PCR扩增反应中。然后可以通过对PCR产物进行可视化或放射性比较来确定靶基因的初始量。我们表明,竞争性PCR MIMICS可用于准确测量mRNA水平的微小变化。