Sepp R, Szabó I, Uda H, Sakamoto H
2nd Department of Pathology, Kagawa Medical School, Japan.
J Clin Pathol. 1994 Apr;47(4):318-23. doi: 10.1136/jcp.47.4.318.
To evaluate the ability of four rapid DNA extraction methods to provide DNA for the polymerase chain reaction (PCR) from routinely fixed, paraffin wax embedded archival tissues.
Eighteen blocks of various tissues, 18 blocks of cervical cancer specimens, and nine blocks of B cell lymphomas were investigated. Both normal and biopsy specimen sized tissues were studied. DNA was extracted using four methods: boiling for 20 minutes in distilled water; boiling for 20 minutes in 5% Chelex-100 resin solution; 3-hour proteinase K digestion; and 3-hour proteinase K digestion, followed by boiling in 5% Chelex-100. Different exons of the p53 gene, human papillomavirus type 16 (HPV 16) sequence, and immunoglobulin heavy chain (IgH) gene rearrangement were amplified from the extracts.
The Chelex boiling, proteinase K digestion, and proteinase K digestion-Chelex boiling methods produced DNA suitable for amplification in all of the 45 samples. Boiling in water yielded insufficient template for the PCR in three of the 45 cases (7%), and in six of 42 positive cases (14%) much fainter bands were observed, mostly when the processed material was either biopsy specimen sized or a B cell lymphoma sample. Fragments of the p53 gene were successfully amplified up to 408 base pairs in water boiled extracts, up to 647 in Chelex boiled preparates, and up to 984 in proteinase K digested and proteinase K digested-Chelex boiled samples, although with decreased sensitivity in the last case. All of the templates were reusable after 3 months of storage at -20 degrees C.
Chelex boiling, proteinase K digestion, and proteinase K digestion followed by Chelex boiling produce suitable templates for the PCR from a large variety of paraffin wax embedded tissues. As the simple 20 minute boiling method in 5% Chelex-100 solution requires minimal manipulation and time, it could be useful, especially in the routine processing of large amounts of material.
评估四种快速DNA提取方法从常规固定、石蜡包埋存档组织中提取用于聚合酶链反应(PCR)的DNA的能力。
研究了18个不同组织块、18个宫颈癌标本块和9个B细胞淋巴瘤块。对正常组织和活检标本大小的组织均进行了研究。使用四种方法提取DNA:在蒸馏水中煮沸20分钟;在5% Chelex-100树脂溶液中煮沸20分钟;蛋白酶K消化3小时;蛋白酶K消化3小时,然后在5% Chelex-100中煮沸。从提取物中扩增p53基因的不同外显子、人乳头瘤病毒16型(HPV 16)序列和免疫球蛋白重链(IgH)基因重排。
Chelex煮沸法、蛋白酶K消化法以及蛋白酶K消化后Chelex煮沸法在所有45个样本中均产生了适合扩增的DNA。在水中煮沸的方法在45个病例中有3个(7%)产生的模板不足以用于PCR,在42个阳性病例中有6个(14%)观察到条带明显较淡,主要是在处理的材料为活检标本大小或B细胞淋巴瘤样本时。在水中煮沸的提取物中,p53基因片段成功扩增至408个碱基对,在Chelex煮沸的制剂中扩增至647个碱基对,在蛋白酶K消化和蛋白酶K消化后Chelex煮沸的样本中扩增至984个碱基对,尽管最后一种情况敏感性有所降低。所有模板在-20℃储存3个月后均可重复使用。
Chelex煮沸法、蛋白酶K消化法以及蛋白酶K消化后Chelex煮沸法能从多种石蜡包埋组织中产生适合PCR的模板。由于在5% Chelex-100溶液中简单煮沸20分钟的方法所需操作和时间最少,因此可能很有用,尤其是在大量材料的常规处理中。