Rubin E, Levy A A
Department of Plant Genetics, Weizmann Institute of Science, Rehovot, Israel.
Nucleic Acids Res. 1996 Sep 15;24(18):3538-45. doi: 10.1093/nar/24.18.3538.
A mathematical model and a computer simulation were used to study PCR specificity. The model describes the occurrences of non-targeted PCR products formed through random primer-template interactions. The PCR simulation scans DNA sequence databases with primers pairs. According to the model prediction, PCR with complex templates should rarely yield non-targeted products under typical reaction conditions. This is surprising as such products are often amplified in real PCR under conditions optimized for stringency. The causes for this 'PCR paradox' were investigated by comparing the model predictions with simulation results. We found that deviations from randomness in sequences from real genomes could not explain the frequent occurrence of non-targeted products in real PCR. The most likely explanation to the 'PCR paradox' is a relatively high tolerance of PCR to mismatches. The model also predicts that mismatch tolerance has the strongest effect on the number of non-targeted products, followed by primer length, template size and product size limit. The model and the simulation can be utilized for PCR studies, primer design and probing DNA uniqueness and randomness.
使用数学模型和计算机模拟来研究聚合酶链反应(PCR)的特异性。该模型描述了通过随机引物-模板相互作用形成的非靶向PCR产物的出现情况。PCR模拟用引物对扫描DNA序列数据库。根据模型预测,在典型反应条件下,使用复杂模板的PCR很少会产生非靶向产物。这令人惊讶,因为在针对严格性进行优化的条件下,此类产物在实际PCR中经常被扩增。通过将模型预测与模拟结果进行比较,研究了这种“PCR悖论”的原因。我们发现,来自真实基因组的序列与随机性的偏差无法解释实际PCR中非靶向产物的频繁出现。对“PCR悖论”最可能的解释是PCR对错配具有相对较高的耐受性。该模型还预测,错配耐受性对非靶向产物数量的影响最大,其次是引物长度、模板大小和产物大小限制。该模型和模拟可用于PCR研究、引物设计以及探究DNA的独特性和随机性。