BMC Biotechnology | |
Automated serial extraction of DNA and RNA from biobanked tissue specimens | |
Lucy Mathot1  Monica Wallin1  Tobias Sjöblom1  | |
[1] Science for Life Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, SE-751 85, Uppsala, Sweden | |
关键词: Tissue biobanking; Sample preparation; Open automation; Cancer; Nucleic acid extraction; | |
Others : 1089660 DOI : 10.1186/1472-6750-13-66 |
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received in 2012-08-13, accepted in 2013-08-15, 发布年份 2013 | |
【 摘 要 】
Background
With increasing biobanking of biological samples, methods for large scale extraction of nucleic acids are in demand. The lack of such techniques designed for extraction from tissues results in a bottleneck in downstream genetic analyses, particularly in the field of cancer research. We have developed an automated procedure for tissue homogenization and extraction of DNA and RNA into separate fractions from the same frozen tissue specimen. A purpose developed magnetic bead based technology to serially extract both DNA and RNA from tissues was automated on a Tecan Freedom Evo robotic workstation.
Results
864 fresh-frozen human normal and tumor tissue samples from breast and colon were serially extracted in batches of 96 samples. Yields and quality of DNA and RNA were determined. The DNA was evaluated in several downstream analyses, and the stability of RNA was determined after 9 months of storage. The extracted DNA performed consistently well in processes including PCR-based STR analysis, HaloPlex selection and deep sequencing on an Illumina platform, and gene copy number analysis using microarrays. The RNA has performed well in RT-PCR analyses and maintains integrity upon storage.
Conclusions
The technology described here enables the processing of many tissue samples simultaneously with a high quality product and a time and cost reduction for the user. This reduces the sample preparation bottleneck in cancer research. The open automation format also enables integration with upstream and downstream devices for automated sample quantitation or storage.
【 授权许可】
2013 Mathot et al.; licensee BioMed Central Ltd.
【 预 览 】
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20150126012439677.pdf | 633KB | download | |
Figure 4. | 59KB | Image | download |
Figure 3. | 48KB | Image | download |
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Figure 1. | 96KB | Image | download |
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【 参考文献 】
- [1]Botling J, Micke P: Fresh frozen tissue: RNA extraction and quality control. Methods Mol Biol 2011, 675:405-413.
- [2]Micke P, Ohshima M, Tahmasebpoor S, Ren ZP, Ostman A, Pontén F, et al.: Biobanking of fresh frozen tissue: RNA is stable in nonfixed surgical specimens. Lab Invest 2006, 86:202-211.
- [3]Hong SH, Baek HA, Jang KY, Chung MJ, Moon WS, Kang MJ, et al.: Effects of delay in the snap freezing of colorectal cancer tissues on the quality of DNA and RNA. J Korean Soc Coloproctol 2010, 26:316-323.
- [4]Morente MM, Mager R, Alonso S, Pezzella F, Spatz A, Knox K, et al.: TuBaFrost 2: Standardising tissue collection and quality control procedures for a European virtual frozen tissue bank network. Eur J Cancer 2006, 42:2684-2691.
- [5]Mathot L, Lindman M, Sjöblom T: Efficient and scalable serial extraction of DNA and RNA from frozen tissue samples. Chem Commun 2011, 47:547-549.
- [6]Reiser V, Smith RC, Xue J, Kurtz MM, Liu R, Legrand C, et al.: High-throughput simultaneous analysis of RNA, protein, and lipid biomarkers in heterogeneous tissue samples. Clin chem 2011, 57:1545-1555.
- [7]Dahl F, Stenberg J, Fredriksson S, Welch K, Zhang M, Nilsson M, et al.: Multigene amplification and massively parallel sequencing for cancer mutation discovery. Proc Natl Acad Sci U S A 2007, 104:9387-9392.
- [8]Bentley DR, Balasubramanian S, Swerdlow HP, Smith GP, Milton J, Brown CG, et al.: Accurate whole human genome sequencing using reversible terminator chemistry. Nature 2008, 456:53-59.
- [9]Glasel JA: Validity of nucleic acid purities monitored by 260nm/280nm absorbance ratios. Biotechniques 1995, 18:62-63.
- [10]Thermo Scientific: Assessment of Nucleic Acid Purity. Wilmington, Delaware USA: NanoDrop Spectrophotometers; [cited 2013 16th August]; Technical Bulletin T042]; Available from: http://www.nanodrop.com/Library/T042-NanoDrop-Spectrophotometers-Nucleic-Acid-Purity-Ratios.pdf webcite
- [11]Coenen MJ, Ploeg M, Schijvenaars MM, Cornel EB, Karthaus HF, Scheffer H, et al.: Allelic imbalance analysis using a single-nucleotide polymorphism microarray for the detection of bladder cancer recurrence. Clin Cancer Res 2008, 14:8198-8204.
- [12]Sjöblom T, Jones S, Wood LD, Parsons DW, Lin J, Barber TD, et al.: The consensus coding sequences of human breast and colorectal cancers. Science 2006, 314:268-274.
- [13]Schroeder A, Mueller O, Stocker S, Salowsky R, Leiber M, Gassmann M, et al.: The RIN: an RNA integrity number for assigning integrity values to RNA measurements. BMC Mol Biol 2006, 7:3. BioMed Central Full Text
- [14]Mathot L, Falk-Sorqvist E, Moens L, Allen M, Sjoblom T, Nilsson M: Automated genotyping of biobank samples by multiplex amplification of insertion/deletion polymorphisms. PloS one 2012, 7(12):e52750.