McKeown B J, Lyndon G J, Andersen J F
Metropolitan Police Forensic Science Laboratory, London, UK.
Biotechniques. 1994 Nov;17(5):901-8.
We demonstrate the potential to generate unambiguous minisatellite variant repeat PCR profiles on an automated DNA sequencer using fluorescent dye-labeled primers. The products of a 24-cycle PCR amplification using 100 ng of template DNA were analyzed by conventional blot hybridization and also on an Applied Biosystems 373A DNA Sequencer. The results from the sequencer were clear to the 20th repeat when using a primer labeled with 6-FAM, whereas conventional analysis allowed codes to be defined to in excess of the 60th repeat. Use of a modified Tag primer sequence, which eliminates the potential for self-annealing, did not improve the clarity of the results under the PCR cycling conditions used.
我们展示了使用荧光染料标记引物在自动DNA测序仪上生成明确的小卫星变异重复PCR图谱的潜力。使用100 ng模板DNA进行24个循环的PCR扩增产物,通过传统的印迹杂交以及在Applied Biosystems 373A DNA测序仪上进行分析。当使用用6-FAM标记的引物时,测序仪的结果在第20个重复时清晰可见,而传统分析允许在超过第60个重复时定义编码。在所用的PCR循环条件下,使用消除了自我退火可能性的改良Tag引物序列并没有提高结果的清晰度。