Forensic labs globally face the same problem growing need to process a greater number and wider variety of samples for DNA analysis.DNA purification step has been thought to be essential for typing of STR DNA. However, this process is time-consuming, and there is a risk of unexpected cross-contamination during purification. There is a need, for each sample type, to develop new methodology that is not only faster but also more reliable than past procedures. FTA technologies provides use most reliable method for DNA extraction.FTA is a chemical treatment of paper, unique to Whatman Bioscience, and is used for the stabilization and storage of biological samples. The FTA matrix is chemically treated with proprietary reagents that lyse cells upon contact. FTA cards protect nucleic acids from nucleases, oxidation, UV damage and microbial and fungal attack. In forensic laboratory there is a need of such a method by which DNA can be extracted by simple method in less time. Here, the method is modified for semen and saliva samples for extraction of DNA on FTA classic cards for forensic use. All the samples were collected only on FTA Classic cards. After DNA extraction, amplification of DNA was carried out then the amplified DNA was placed into DNA sequencer for STR profiling. STR peaks were obtained from the all biological samples such as Blood, Saliva and Semen in our study thus there is no need of other kits available for collection of samples. On the basis of results, it is considered that modified procedure using an FTA card can be applicable to routine work.
Patel Jignal, M.G.Shaikh and Marjadi Darshan., Forensic Conception: Dna Typing of Fta Spotted Samples. J App Biol Biotech, 2014; 2 (04): 021-029. DOI: 10.7324/JABB.2014.2404
1. Yoshida K, Sekiguchi K, Mizuno N, Kasai K, Sakai I, Sato H, Seta S. The modified method of two-step differential extraction of sperm and vaginal epithelial cell DNA from vaginal fluid mixed with semen. Forensic Sci Int 1995; 72:25–33.
2. Whatman Inc. [2002]; FTA Protocols: Collect, Transport, Archive and Access Nucleic Acids – All at Room Temperature; WB120047; Available at www.whatman.com
3. Whatman Inc. [2002]; FTA Protocol BD08, Preparing an FTA® Disc for DNA Analysis, Available at www.whatman.com
4. Whatman Inc. [2011]; Whatman FTA technology overview (Brochure). GE Healthcare Life Sciences , UK limited.
5. Pankaj Shrivastava , Veena Ben Trivedi , Anil K Singh and N.Mishra Application of DNA fingerprinting technology in forensic investigation. International Journal of Scientific and Research Publications, Volume 2, Issue 10, October 2012.
6. forensicdnacenter.com[Internet].DNA Diagnostic Center, DNA testing system, Short tandem repeats[1995 – 2008] , Available at www.forensicdnacenter.com
7. Whatman Inc. [2011]; FTA cards from GE Healthcare are chemically coated matrices that have been shown to preserve DNA more efficiently than untreated matrices (Brochure). GE Healthcare Life Sciences, UK limited
8. Whatman Inc. [2003-2010]; FTA- A highly flexible technology used widely in a range of technology (Brochure).GE Health Care Life Sciences, UK limited.
9. Lutz Roewer. Y chromosome STR typing in crime casework.Forensic Sci Med Pathol.2009;5:77–84
10. John M. Butler and Dennis J. Reeder (NIST Biochemical Science Division).Short Tandem Repeat DNA Internet Database, Forensic STR Information. Available from: http://www.cstl.nist.gov/strbase/
11. Beckett, S.M., S.J. Laughton, L.D. Pozza ,G. B. Mc Cowage, G. Marshall, R.J. Cohn, E. Milne, and L.J. Ashton. Buccal swabs and treated cards: methodological considerations for molecular epidemiologic. Am. J. Epidemiol.2008;167:1260-1267.
12. Zhou, H., J.G.H. Hickford, and Q. Fang. A two-step procedure for extracting genomic DNA from dried blood spots on filter paper for polymerase chain reaction amplification. Anal. Biochem. 2006; 354:159-161.
13. Hansen, T.V.O., M.K. Simonsen, F.C. Nielsen, and Y.A. Hundrup. Collection of blood, saliva, and buccal cell samples in a pilot study on the danish nurse cohort: comparison of the response rate and quality of genomic DNA. Cancer Epidemiol. Biomarkers Prev. 2007;16:2072- 2076.
14. Passmore, L.A., B. Kaesmann-Kellner, and B.H.F. Weber. Novel and recurrent mutations in the tyrosinase gene and the P gene in the German albino population. Hum. Genet. 1999;105:200-210.
15. Walker AH, Najarian D, White DL, et al. Collection of genomic DNA by buccal swabs for polymerase chain reaction-based biomarker assays. Environ Health Perspect 1999;107:517 – 20.
16. Kozlowski LT, Vogler GR, Vandenbergh DJ, et al. Using a telephone survey to acquire genetic and behavioral data related to cigarette smoking in ‘‘madeanonymous’’ and ‘‘registry’’ samples. Am J Epidemiol 2002;156:68– 77.
17. King IB, Satia-Abouta J, Thornquist MD, et al. Buccal cell DNA yield, quality, and collection costs: comparison of methods for large-scale studies. Cancer Epidemiol Biomarkers Prev 2002;11:1130 – 3.
18. Garcia-Closas M, Egan KM, Abruzzo J, et al. Collection of genomic DNA from adults in epidemiological studies by buccal cytobrush and mouthwash. Cancer Epidemiol Biomarkers Prev 2001;10:687 – 96.
19. Le Marchand L, Lum-Jones A, Saltzman B, et al. Feasibility of collecting buccal cell DNA by mail in a cohort study. Cancer Epidemiol Biomarkers Prev 2001;10:701 – 3.
20. Yang YG, Kim JY, Song YH, Kim DS. A novel buffer system, AnyDirect, can improve polymerase chain reaction from whole blood without DNA isolation. Clin Chim Acta 2007;380:112–7.
21. Yang YG, Kim JY, Soh MS, Kim DS. A simple and rapid gene amplification from Arabidopsis leaves using AnyDirect system. J Biochem Mol Biol 2007;40(3):444–7.
22. McCusker J, Dawson MT, Noone D, Gannon F, Smith T. Improved method for direct PCR amplification from whole blood. Nucleic Acids Res 1992; 20:6747.
23. Park SJ, Woo KM, Oh HH, Kim SH, Lee SH. Population data of the 25 STR loci in Koreans. J Forensic Sci 2005;50:710–2.
24. Yang YG, Kim JY, Kim SW, Lee SG, Inventors. Methods for performing direct enzymatic reactions involving nucleic acid molecules. Patent WO 090987 (Rep. of Korea PCT ⁄ KR 000457) 2006.
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