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Erschienen in: International Journal of Legal Medicine 3/2020

15.08.2019 | Method Paper

Development and forensic validation of human genomic DNA quantification kit

verfasst von: Jeongyong Kim, Ju Yeon Jung, So Yeun Kwon, Pilwon Kang, Hyunchul Park, Ki min Seong, Tae ue Kim, Hyeon Kyu Yoon, Si-Keun Lim

Erschienen in: International Journal of Legal Medicine | Ausgabe 3/2020

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Abstract

DNA quantification is an essential step for successful multiplex short tandem repeat (STR) polymerase chain reactions (PCR), which are used for confirming identities using human genomic DNA. The new DNA quantification kit, named the National Forensic Service Quantification (NFSQ) kit, simultaneously provides total human DNA concentration, human male DNA concentration, and a DNA degradation index (DI) using multiplex TaqMan fluorescent probes. The NFSQ was validated according to developmental validation guidelines from the SWGDAM and MIQE. NFSQ detected up to 0.00128 ng/μL and could detect male DNA up to a 1:8000 ratio of male to female DNA. In PCR inhibitor tests, NFSQ could measure DNA at a concentration of 200 ng/μL of humic acid and 600 μM of hematin. The NFSQ kit showed a DI value trend similar to other qPCR kits. In the reproducibility study, the coefficient of variation of the NFSQ kit was within 10%. The quantitative results of the casework samples obtained using the NFSQ kit were consistent with the STR interpretation results. The NFSQ kit can be useful in the human identification process, as it has detection capabilities similar to those of other comparable quantification kits.
Literatur
1.
Zurück zum Zitat Butler JM (2011) Advanced topics in forensic DNA typing: methodology. National Institute of standards and Technology, Gaithersburg Butler JM (2011) Advanced topics in forensic DNA typing: methodology. National Institute of standards and Technology, Gaithersburg
2.
Zurück zum Zitat Kitayama T, Fujii K, Nakahara H, Mizuno N, Kasai K, Yonezawa N, Sekiguchi K (2013) Estimation of the detection rate in STR analysis by determining the DNA degradation ratio using quantitative PCR. Legal Med 15:1–6CrossRef Kitayama T, Fujii K, Nakahara H, Mizuno N, Kasai K, Yonezawa N, Sekiguchi K (2013) Estimation of the detection rate in STR analysis by determining the DNA degradation ratio using quantitative PCR. Legal Med 15:1–6CrossRef
3.
Zurück zum Zitat Ambers A, Turnbough M, Benjamin R, Gill-King H, King J, Sajantila A, Budowle B (2016) Modified DOP-PCR for improved STR typing of degraded DNA from human skeletal remains and bloodstains. Legal Med 18:7–12CrossRef Ambers A, Turnbough M, Benjamin R, Gill-King H, King J, Sajantila A, Budowle B (2016) Modified DOP-PCR for improved STR typing of degraded DNA from human skeletal remains and bloodstains. Legal Med 18:7–12CrossRef
4.
Zurück zum Zitat Butler JM (2006) Genetics and genomics of core short tandem repeat loci used in human identity. J Forensic Sci 51(2):253–265CrossRef Butler JM (2006) Genetics and genomics of core short tandem repeat loci used in human identity. J Forensic Sci 51(2):253–265CrossRef
5.
Zurück zum Zitat Kline MC, Duewer DL, Redman JW, Butler JM (2003) Mixed stain study 3: DNA quantitation accuracy and its influence on short tandem repeat multiplex signal intensity. Anal Chem 46(5):1199–1210 Kline MC, Duewer DL, Redman JW, Butler JM (2003) Mixed stain study 3: DNA quantitation accuracy and its influence on short tandem repeat multiplex signal intensity. Anal Chem 46(5):1199–1210
6.
Zurück zum Zitat Lee SB, McCord B, Buel E (2014) Advances in forensic DNA quantification: a review. Electrophoresis 35(21–22):3044–3052CrossRef Lee SB, McCord B, Buel E (2014) Advances in forensic DNA quantification: a review. Electrophoresis 35(21–22):3044–3052CrossRef
7.
Zurück zum Zitat Nielsen K, Mogensen HS, Hedman J, Niederstätter H, Parson W, Morling N (2008) Comparison of five DNA quantification methods. Forensic Sci Int Genet 2:226–230CrossRef Nielsen K, Mogensen HS, Hedman J, Niederstätter H, Parson W, Morling N (2008) Comparison of five DNA quantification methods. Forensic Sci Int Genet 2:226–230CrossRef
8.
Zurück zum Zitat Deagle BE, Eveson JP, Buel E (2006) Quantification of damage in DNA recovered from highly degraded samples-a case study on DNA in faeces. Front Zool 3:11CrossRef Deagle BE, Eveson JP, Buel E (2006) Quantification of damage in DNA recovered from highly degraded samples-a case study on DNA in faeces. Front Zool 3:11CrossRef
9.
Zurück zum Zitat Alonso A, Martin P, Albarran C, Garcia P, Garcia O, Fernandez de Simon L, Garcia-Hirschfeld J, Sancho M, de la Rua C, Fernandez-Piqueras J (2004) Real-time PCR designs to estimate nuclear and mitochondrial DNA copy number in forensic and ancient DNA studies. Forensic Sci Int 139:141–149CrossRef Alonso A, Martin P, Albarran C, Garcia P, Garcia O, Fernandez de Simon L, Garcia-Hirschfeld J, Sancho M, de la Rua C, Fernandez-Piqueras J (2004) Real-time PCR designs to estimate nuclear and mitochondrial DNA copy number in forensic and ancient DNA studies. Forensic Sci Int 139:141–149CrossRef
10.
Zurück zum Zitat Van Guilder HD, Vrana KE, Freeman WM (2008) Twenty-five years of quantitative PCR for gene expression analysis. Biotechniques 44(5):619–626CrossRef Van Guilder HD, Vrana KE, Freeman WM (2008) Twenty-five years of quantitative PCR for gene expression analysis. Biotechniques 44(5):619–626CrossRef
11.
Zurück zum Zitat Udvardi MK, Czechowski T, Scheible WR (2008) Eleven Golden rules of quantitative RT-PCR. Plant Cell 20(7):1736–1737CrossRef Udvardi MK, Czechowski T, Scheible WR (2008) Eleven Golden rules of quantitative RT-PCR. Plant Cell 20(7):1736–1737CrossRef
13.
Zurück zum Zitat Lin SW, Li C, Ip SCY (2018) A performance study on three qPCR quantification kits and their compatibilities with the 6-dye DNA profiling systems. Forensic Sci Int Genet 33:72–83CrossRef Lin SW, Li C, Ip SCY (2018) A performance study on three qPCR quantification kits and their compatibilities with the 6-dye DNA profiling systems. Forensic Sci Int Genet 33:72–83CrossRef
14.
Zurück zum Zitat Stephen AB, Vladimir B, Jeremy AG, Jan H, Jim H, Mikael K, Reinhold M, Tania N, Michael WP, Gregory LS, Jo V (2009) Carl TW (2009) the MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments. Clin Chem 55(4):611–622CrossRef Stephen AB, Vladimir B, Jeremy AG, Jan H, Jim H, Mikael K, Reinhold M, Tania N, Michael WP, Gregory LS, Jo V (2009) Carl TW (2009) the MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments. Clin Chem 55(4):611–622CrossRef
15.
Zurück zum Zitat McMichael GL, Highet AR (2011) Comparison of DNA extraction methods from small samples of newborn screening cards suitable for retrospective perinatal viral research. J Biomol Tech 22(1):5–9PubMedPubMedCentral McMichael GL, Highet AR (2011) Comparison of DNA extraction methods from small samples of newborn screening cards suitable for retrospective perinatal viral research. J Biomol Tech 22(1):5–9PubMedPubMedCentral
17.
Zurück zum Zitat Girish PS, Anjaneyulu AS, Viswas KN, Anand M, Rajkumar N, Shivakumar BM, Bhaskar S (2004) Sequence analysis of mitochondrial 12S rRNA gene can identify meat species. Meat Sci 66(3):551–556CrossRef Girish PS, Anjaneyulu AS, Viswas KN, Anand M, Rajkumar N, Shivakumar BM, Bhaskar S (2004) Sequence analysis of mitochondrial 12S rRNA gene can identify meat species. Meat Sci 66(3):551–556CrossRef
18.
Zurück zum Zitat Swango KL, Timken MD, Date Chong M, Buoncristiani MR (2006) A quantitative PCR assay for the assessment of DNA degradation in forensic samples. Forensic Sci Int 158:14–26CrossRef Swango KL, Timken MD, Date Chong M, Buoncristiani MR (2006) A quantitative PCR assay for the assessment of DNA degradation in forensic samples. Forensic Sci Int 158:14–26CrossRef
19.
Zurück zum Zitat Elsner HI, Lindblad EB (1989) Ultrasonic degradation of DNA. DNA 8(10):697–701CrossRef Elsner HI, Lindblad EB (1989) Ultrasonic degradation of DNA. DNA 8(10):697–701CrossRef
20.
Zurück zum Zitat Swango KL, Hudlow WR, Timken MD, Buoristiani MR (2007) Developmental validation of a multiplex qPCR assay for assessing the quantity and quality of nuclear DNA in forensic samples. Forensic Sci Int 170:35–45CrossRef Swango KL, Hudlow WR, Timken MD, Buoristiani MR (2007) Developmental validation of a multiplex qPCR assay for assessing the quantity and quality of nuclear DNA in forensic samples. Forensic Sci Int 170:35–45CrossRef
21.
Zurück zum Zitat Holt A, Wootton SC, Mulero JJ, Brzoska PM, Langit E, Green RL (2016) Developmental validation of the Quantifiler® HP and trio kits for human DNA quantification in forensic samples. Forensic Sci Int Genet 21:145–157CrossRef Holt A, Wootton SC, Mulero JJ, Brzoska PM, Langit E, Green RL (2016) Developmental validation of the Quantifiler® HP and trio kits for human DNA quantification in forensic samples. Forensic Sci Int Genet 21:145–157CrossRef
22.
Zurück zum Zitat Maura Barbisin, Rixun Fang, Cristin E. O’Shea, Lisa M. Calandro, Monohar R. Furtado, J.G. Shewale (2009) Developmental validation of the Quantifiler® duo DNA quantification kit for simultaneous quantification of total human and human male DNA and detection of PCR inhibitors in biological samples. J Forensic Sci 54305–319, 54, 305 Maura Barbisin, Rixun Fang, Cristin E. O’Shea, Lisa M. Calandro, Monohar R. Furtado, J.G. Shewale (2009) Developmental validation of the Quantifiler® duo DNA quantification kit for simultaneous quantification of total human and human male DNA and detection of PCR inhibitors in biological samples. J Forensic Sci 54305–319, 54, 305
26.
Zurück zum Zitat Schaiff WT, Hruska KA Jr, McCourt DW, Green M, Schwartz BD (1992) HLA-DR associates with specific stress proteins and is retained in the endoplasmic reticulum in invariant chain negative cells. J Exp Med 176(3):657–666CrossRef Schaiff WT, Hruska KA Jr, McCourt DW, Green M, Schwartz BD (1992) HLA-DR associates with specific stress proteins and is retained in the endoplasmic reticulum in invariant chain negative cells. J Exp Med 176(3):657–666CrossRef
27.
Zurück zum Zitat Jonsson AK, Rask L (1989) Human class II DNA and DOB genes display low sequence variability. Immunogenetics 29(6):411–413CrossRef Jonsson AK, Rask L (1989) Human class II DNA and DOB genes display low sequence variability. Immunogenetics 29(6):411–413CrossRef
29.
Zurück zum Zitat Holmes AS, Houston R, Elwick K, Gangitano D, Hughes-Stamm S (2017) Evaluation of four commercial quantitative real-time PCR kits with inhibited and degraded samples. Int J Legal Med 129:1–11 Holmes AS, Houston R, Elwick K, Gangitano D, Hughes-Stamm S (2017) Evaluation of four commercial quantitative real-time PCR kits with inhibited and degraded samples. Int J Legal Med 129:1–11
30.
Zurück zum Zitat Karni M, Zidon D, Polak P, Zalevsky Z, Shefi O (2013) Thermal degradation of DNA. DNA Cell Biol 32:298–301CrossRef Karni M, Zidon D, Polak P, Zalevsky Z, Shefi O (2013) Thermal degradation of DNA. DNA Cell Biol 32:298–301CrossRef
31.
Zurück zum Zitat Cho Y, Kim HS, Kim MH, Park M, Kwon H, Lee YH, Lee DS (2018) Validation of reduced reagent volumes in the implementation of the Quantifiler® trio DNA quantification kit. J Forensic Sci 63(2):517–525CrossRef Cho Y, Kim HS, Kim MH, Park M, Kwon H, Lee YH, Lee DS (2018) Validation of reduced reagent volumes in the implementation of the Quantifiler® trio DNA quantification kit. J Forensic Sci 63(2):517–525CrossRef
32.
Zurück zum Zitat Goecker ZC, Swiontek SE, Lakhtakia A, Roy R (2016) Comparison of Quantifiler® trio and InnoQuant™ human DNA quantification kits for detection of DNA degradation in developed and aged fingerprints. Forensic Sci Int 263:132–138CrossRef Goecker ZC, Swiontek SE, Lakhtakia A, Roy R (2016) Comparison of Quantifiler® trio and InnoQuant™ human DNA quantification kits for detection of DNA degradation in developed and aged fingerprints. Forensic Sci Int 263:132–138CrossRef
33.
Zurück zum Zitat Ewing MM, Thompson JM, McLaren RS, Purpero VM, Thomas KJ, Dobrowski PA, DeGroot GA, Romsos EL, Storts DR (2016) Human DNA quantification and sample quality assessment: developmental validation of the PowerQuant® system. Forensic Sci Int Genet 23:166–177CrossRef Ewing MM, Thompson JM, McLaren RS, Purpero VM, Thomas KJ, Dobrowski PA, DeGroot GA, Romsos EL, Storts DR (2016) Human DNA quantification and sample quality assessment: developmental validation of the PowerQuant® system. Forensic Sci Int Genet 23:166–177CrossRef
34.
Zurück zum Zitat Vranes M, Scherer M, Elliott K (2017) Development and validation of the Investigator® Quantiplex Pro kit for qPCR-based examination of the quantity and quality of human DNA in forensic samples. Forensic Sci Int Genet Suppl Ser 6:e518–e519CrossRef Vranes M, Scherer M, Elliott K (2017) Development and validation of the Investigator® Quantiplex Pro kit for qPCR-based examination of the quantity and quality of human DNA in forensic samples. Forensic Sci Int Genet Suppl Ser 6:e518–e519CrossRef
Metadaten
Titel
Development and forensic validation of human genomic DNA quantification kit
verfasst von
Jeongyong Kim
Ju Yeon Jung
So Yeun Kwon
Pilwon Kang
Hyunchul Park
Ki min Seong
Tae ue Kim
Hyeon Kyu Yoon
Si-Keun Lim
Publikationsdatum
15.08.2019
Verlag
Springer Berlin Heidelberg
Erschienen in
International Journal of Legal Medicine / Ausgabe 3/2020
Print ISSN: 0937-9827
Elektronische ISSN: 1437-1596
DOI
https://doi.org/10.1007/s00414-019-02131-z

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