Zada Almira, Susanto Puspasari S, Putri Raden L, Sahiratmadja Edhyana K, Hernowo Bethy S, Rezano Andri, Sribudiani Yunia
Department of Biomedical Sciences, Division of Biochemistry and Molecular Biology, Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia.
Research Center of Medical Genetics, Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia.
Cell Mol Biol (Noisy-le-grand). 2018 Oct 30;64(13):38-41.
The tissue sample may have important genetic information in diagnostic, prognostic and counselling issues. Formalin-Fixed-Paraffin-Embedded (FFPE) is a routine method for preserving tissues. However, DNA isolated from FFPE tissue is often difficult to be amplified in PCR due to fragmentation and DNA-protein crosslinks. This study aimed to optimize the DNA isolation method from FFPE tissue and compare the performance of four different PCR ready-to-use kits. Genomic DNA was isolated from FFPE tissue colon of Short-segment Hirschsprung (S-HSCR) patients and prostate cancer tissue using Quick-DNA™ FFPE Kit (Zymo Research) with and without pre-heating treatment in KOH/NOH solution. Primers for Androgen Receptor (AR) gene and four different PCR kits: MyTaq HS Red Mix 2X (BioLine), FastStart Taq DNA Polymerase (Roche), KAPA2G fast PCR Kit 2X (KAPA Biosystem) and KOD FX Neo (Toyobo) were used for amplification. DNA electrophoresis was performed to compare the PCR results. BioLine and Toyobo kits gave better PCR results than those of Roche and KAPA Biosystem. Increasing amount of Taq polymerase and dNTPs of Roche kit by two-fold could increase the quality of PCR results. Toyobo could amplify DNA up to 417 bp, however, none of these PCR kits could amplify DNA above 450 bp. Pre-heated treatment of FFPE tissue in NaOH/KOH did not improve the DNA quality and PCR results. Toyobo PCR ready-to-use kit gave the best result among the other three PCR kits used in this study in amplifying DNA isolated from FFPE tissue. Designing the primers producing amplicon not more than 450 bp is suggested.
组织样本在诊断、预后和咨询问题方面可能具有重要的遗传信息。福尔马林固定石蜡包埋(FFPE)是保存组织的常规方法。然而,从FFPE组织中分离的DNA由于片段化和DNA-蛋白质交联,在PCR中往往难以扩增。本研究旨在优化从FFPE组织中分离DNA的方法,并比较四种不同即用型PCR试剂盒的性能。使用Quick-DNA™ FFPE试剂盒(Zymo Research),对短节段先天性巨结肠(S-HSCR)患者的FFPE结肠组织和前列腺癌组织进行基因组DNA分离,在KOH/NOH溶液中进行或不进行预热处理。使用雄激素受体(AR)基因的引物和四种不同的PCR试剂盒:MyTaq HS Red Mix 2X(BioLine)、FastStart Taq DNA聚合酶(罗氏)、KAPA2G fast PCR试剂盒2X(KAPA生物系统)和KOD FX Neo(东洋纺)进行扩增。进行DNA电泳以比较PCR结果。BioLine和东洋纺试剂盒的PCR结果优于罗氏和KAPA生物系统。将罗氏试剂盒的Taq聚合酶和dNTPs量增加两倍可提高PCR结果的质量。东洋纺可扩增至417 bp的DNA,但这些PCR试剂盒均无法扩增450 bp以上的DNA。FFPE组织在NaOH/KOH中的预热处理并未提高DNA质量和PCR结果。在本研究中使用的其他三种PCR试剂盒中,东洋纺即用型PCR试剂盒在扩增从FFPE组织中分离的DNA方面效果最佳。建议设计产生不超过450 bp扩增子的引物。