Sara Kazmi, Bella Khatib-Shahidi, John Najjar, Anish Sharma, Caitlin Murphy, Humza Bashir, Benjamin French, Apurva Lad, David Kennedy, Steven Haller
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Storage duration, tissue handling and tissue preservation processes as well as their interactions with the nucleic acids could influence the quality and integrity of the DNA or RNA required for genetic analysis. \nObjectives: The goal of this study was to establish a protocol to extract high quality DNA and RNA from the FFPE tissues for further use in quantitative PCR analysis. \nMethods: For the purposes of this study, human FFPE biopsy tissues from lung, liver, colon and kidney were obtained from a single center biorepository. GeneJET Genomic DNA Purification Kit (Catalog # K0722) obtained from Thermo Fisher Scientific and RecoverAll Total Nucleic Acid Isolation Kit obtained from Life Technologies were modified and used for extraction of DNA and RNA, respectively. Briefly, modifications involved extending reagent incubation times, increasing sample volumes and wash steps, and increased final nucleic acids recovery and concentration steps. Eight sections around 8-10 ?m thick were microtomed for each tissue sample and used for extraction. The purity of the nucleic acids obtained was verified using Nanodrop Spectrophotometer. \nResults: The average DNA yield from eight sections for each of the tissues was 270±184 ng/?l and for RNA was 296±188 ng/?l. Nucleic acid quality was assessed by measuring the 260nm/280nm absorbance ratio for protein contamination as well as the 260nm/230nm absorbance ratio for salt contamination. Both were found to be within acceptable ranges. RNA was reverse transcribed to cDNA and qPCR was successfully performed on both DNA and cDNA samples. \nConclusions: These results indicate that protocols using the silica-based membrane technology can yield high quality DNA and RNA that can be successfully used for downstream genetic analysis.","PeriodicalId":220681,"journal":{"name":"Translation: The University of Toledo Journal of Medical Sciences","volume":"8 5","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Protocol Development for Yielding High Quality DNA and RNA from Archived Formalin-Fixed Paraffin Embedded Tissues\",\"authors\":\"Sara Kazmi, Bella Khatib-Shahidi, John Najjar, Anish Sharma, Caitlin Murphy, Humza Bashir, Benjamin French, Apurva Lad, David Kennedy, Steven Haller\",\"doi\":\"10.46570/utjms.vol11-2023-939\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: While genetic analysis of archived formalin-fixed paraffin embedded (FFPE) tissue specimens would be a significant research resource, extraction of high-quality DNA and RNA from these specimens is a significant challenge. Storage duration, tissue handling and tissue preservation processes as well as their interactions with the nucleic acids could influence the quality and integrity of the DNA or RNA required for genetic analysis. \\nObjectives: The goal of this study was to establish a protocol to extract high quality DNA and RNA from the FFPE tissues for further use in quantitative PCR analysis. \\nMethods: For the purposes of this study, human FFPE biopsy tissues from lung, liver, colon and kidney were obtained from a single center biorepository. GeneJET Genomic DNA Purification Kit (Catalog # K0722) obtained from Thermo Fisher Scientific and RecoverAll Total Nucleic Acid Isolation Kit obtained from Life Technologies were modified and used for extraction of DNA and RNA, respectively. Briefly, modifications involved extending reagent incubation times, increasing sample volumes and wash steps, and increased final nucleic acids recovery and concentration steps. 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引用次数: 0
摘要
简介虽然对归档的福尔马林固定石蜡包埋(FFPE)组织标本进行遗传分析是一项重要的研究资源,但从这些标本中提取高质量的 DNA 和 RNA 却是一项重大挑战。储存时间、组织处理和组织保存过程以及它们与核酸的相互作用都会影响遗传分析所需的 DNA 或 RNA 的质量和完整性。目标:本研究的目的是制定一套从 FFPE 组织中提取高质量 DNA 和 RNA 的方案,以便进一步用于定量 PCR 分析。方法:本研究从一个中心的生物库中获取了肺部、肝脏、结肠和肾脏的人体 FFPE 活检组织。对 Thermo Fisher Scientific 的 GeneJET 基因组 DNA 纯化试剂盒(目录号 K0722)和 Life Technologies 的 RecoverAll 总核酸分离试剂盒进行了改良,分别用于提取 DNA 和 RNA。简而言之,修改包括延长试剂孵育时间、增加样品量和清洗步骤,以及增加最终核酸回收和浓缩步骤。对每个组织样本进行显微切片,每个切片厚约 8-10 毫米,用于提取。使用纳氏分光光度计验证所获得核酸的纯度。结果:每个组织八个切片的平均 DNA 产量为 270±184 纳克/升,RNA 为 296±188 纳克/升。核酸质量通过测量 260nm/280nm 吸光度比值(蛋白质污染)和 260nm/230nm 吸光度比值(盐污染)来评估。 结果显示,两者均在可接受范围内。将 RNA 反转录为 cDNA,并成功地对 DNA 和 cDNA 样品进行了 qPCR 分析。结论:这些结果表明,使用硅基膜技术的方案可以获得高质量的 DNA 和 RNA,并可成功用于下游基因分析。
Protocol Development for Yielding High Quality DNA and RNA from Archived Formalin-Fixed Paraffin Embedded Tissues
Introduction: While genetic analysis of archived formalin-fixed paraffin embedded (FFPE) tissue specimens would be a significant research resource, extraction of high-quality DNA and RNA from these specimens is a significant challenge. Storage duration, tissue handling and tissue preservation processes as well as their interactions with the nucleic acids could influence the quality and integrity of the DNA or RNA required for genetic analysis.
Objectives: The goal of this study was to establish a protocol to extract high quality DNA and RNA from the FFPE tissues for further use in quantitative PCR analysis.
Methods: For the purposes of this study, human FFPE biopsy tissues from lung, liver, colon and kidney were obtained from a single center biorepository. GeneJET Genomic DNA Purification Kit (Catalog # K0722) obtained from Thermo Fisher Scientific and RecoverAll Total Nucleic Acid Isolation Kit obtained from Life Technologies were modified and used for extraction of DNA and RNA, respectively. Briefly, modifications involved extending reagent incubation times, increasing sample volumes and wash steps, and increased final nucleic acids recovery and concentration steps. Eight sections around 8-10 ?m thick were microtomed for each tissue sample and used for extraction. The purity of the nucleic acids obtained was verified using Nanodrop Spectrophotometer.
Results: The average DNA yield from eight sections for each of the tissues was 270±184 ng/?l and for RNA was 296±188 ng/?l. Nucleic acid quality was assessed by measuring the 260nm/280nm absorbance ratio for protein contamination as well as the 260nm/230nm absorbance ratio for salt contamination. Both were found to be within acceptable ranges. RNA was reverse transcribed to cDNA and qPCR was successfully performed on both DNA and cDNA samples.
Conclusions: These results indicate that protocols using the silica-based membrane technology can yield high quality DNA and RNA that can be successfully used for downstream genetic analysis.