Skip to main content
Erschienen in: International Journal of Legal Medicine 3/2020

06.02.2020 | Original Article

Validation of a 52-mtSNP minisequencing panel for haplogroup classification of forensic DNA samples

verfasst von: Leire Palencia-Madrid, Diana Vinueza-Espinosa, Miriam Baeta, Ana M. Rocandio, Marian M. de Pancorbo

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

Einloggen, um Zugang zu erhalten

Abstract

Mitochondrial DNA (mtDNA) is a useful tool in forensic investigation as it provides information about the matrilineal ancestry of individuals. In addition, mtDNA can be analyzed when the analysis of other nuclear markers is underperforming. Recently, we developed a minisequencing panel for the simultaneous analysis of 52 mtDNA SNPs to classify maternal lineages into the main haplogroups and their phylogeographic origin. In order to make this panel suitable for forensic genetics laboratories, a validation study has been performed in accordance with the Scientific Working Group on DNA Analysis Methods (SWGDAM) guidelines, including species specificity, reproducibility, sensitivity, and stability tests. The results demonstrate that the panel of 52 mtDNA SNPs is highly sensitive, since it enables to obtain complete genetic profiles of samples containing minimal amounts of DNA (1 pg). Furthermore, it provides sufficient genetic information to detect the matrilineal biogeographical origin of highly degraded samples, i.e., ancient dating skeletal remains, and samples with the presence of inhibitors, such as hematin and humic acid. In addition, this panel can detect mixtures in samples whose mtDNA haplogroups of contributors are different. Overall, the results of this study demonstrate the suitability of this minisequencing panel of 52 mtDNA SNPs to be used in forensic cases, with samples of low amount or degraded DNA.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat Machida M, Taki T, Shimada R, Kibayashi K (2016) Investigation of single nucleotide polymorphism loci susceptible to degradation by ultraviolet light. J Forensic Legal Med 43:120–125CrossRef Machida M, Taki T, Shimada R, Kibayashi K (2016) Investigation of single nucleotide polymorphism loci susceptible to degradation by ultraviolet light. J Forensic Legal Med 43:120–125CrossRef
2.
Zurück zum Zitat Lutz S, Weisser HJ, Heizmann J, Pollak S (1998) Location and frequency of polymorphic positions in the mtDNA control region of individuals from Germany. Int J Legal Med 111(2):67–77CrossRef Lutz S, Weisser HJ, Heizmann J, Pollak S (1998) Location and frequency of polymorphic positions in the mtDNA control region of individuals from Germany. Int J Legal Med 111(2):67–77CrossRef
3.
Zurück zum Zitat Just RS, Scheible MK, Fast SA, Sturk-Andreaggi K, Higginbotham JL, Lyons EA, Bush JM, Peck MA, Ring JD, Diegoli TM, Röck AW, Huber GE, Nagl S, Strobl C, Zimmermann B, Parson W, Irwin JA (2014) Development of forensic-quality full mtGenome haplotypes: success rates with low template specimens. Forensic Sci Int Genet 10:73–79CrossRef Just RS, Scheible MK, Fast SA, Sturk-Andreaggi K, Higginbotham JL, Lyons EA, Bush JM, Peck MA, Ring JD, Diegoli TM, Röck AW, Huber GE, Nagl S, Strobl C, Zimmermann B, Parson W, Irwin JA (2014) Development of forensic-quality full mtGenome haplotypes: success rates with low template specimens. Forensic Sci Int Genet 10:73–79CrossRef
4.
Zurück zum Zitat Strobl C, Eduardoff M, Bus MM, Allen M, Parson W (2018) Evaluation of the precision ID whole MtDNA genome panel for forensic analyses. Forensic Sci Int Genet 35:21–25CrossRef Strobl C, Eduardoff M, Bus MM, Allen M, Parson W (2018) Evaluation of the precision ID whole MtDNA genome panel for forensic analyses. Forensic Sci Int Genet 35:21–25CrossRef
5.
Zurück zum Zitat Marshall C, Sturk-Andreaggi K, Daniels-Higginbotham J, Oliver RS, Barritt-Ross S, McMahon TP (2017) Performance evaluation of a mitogenome capture and Illumina sequencing protocol using non-probative, case-type skeletal samples: implications for the use of a positive control in a next-generation sequencing procedure. Forensic Sci Int Genet 31:198–206CrossRef Marshall C, Sturk-Andreaggi K, Daniels-Higginbotham J, Oliver RS, Barritt-Ross S, McMahon TP (2017) Performance evaluation of a mitogenome capture and Illumina sequencing protocol using non-probative, case-type skeletal samples: implications for the use of a positive control in a next-generation sequencing procedure. Forensic Sci Int Genet 31:198–206CrossRef
6.
Zurück zum Zitat Wai KT, Barash M, Gunn P (2018) Performance of the Early Access AmpliSeq™ Mitochondrial Panel with degraded DNA samples using the Ion Torrent™ platform. Electrophoresis 39(21):2776–2784CrossRef Wai KT, Barash M, Gunn P (2018) Performance of the Early Access AmpliSeq™ Mitochondrial Panel with degraded DNA samples using the Ion Torrent™ platform. Electrophoresis 39(21):2776–2784CrossRef
7.
Zurück zum Zitat Parson W, Strobl C, Huber G, Zimmermann B, Gomes SM, Souto L, Fendt L, Delport R, Langit R, Wootton S, Lagacé R, Irwin J (2013) Evaluation of next generation mtGenome sequencing using the Ion Torrent Personal Genome Machine (PGM). Forensic Sci Int Genet 7(5):543–549CrossRef Parson W, Strobl C, Huber G, Zimmermann B, Gomes SM, Souto L, Fendt L, Delport R, Langit R, Wootton S, Lagacé R, Irwin J (2013) Evaluation of next generation mtGenome sequencing using the Ion Torrent Personal Genome Machine (PGM). Forensic Sci Int Genet 7(5):543–549CrossRef
8.
Zurück zum Zitat Peck MA, Brandhagen MD, Marshall C, Diegoli TM, Irwin JA, Sturk-Andreaggi K (2016) Concordance and reproducibility of a next generation mtGenome sequencing method for high-quality samples using the Illumina MiSeq. Forensic Sci Int Genet 24:103–111CrossRef Peck MA, Brandhagen MD, Marshall C, Diegoli TM, Irwin JA, Sturk-Andreaggi K (2016) Concordance and reproducibility of a next generation mtGenome sequencing method for high-quality samples using the Illumina MiSeq. Forensic Sci Int Genet 24:103–111CrossRef
9.
Zurück zum Zitat Mosquera-Miguel A, Alvarez-Iglesias V, Cerezo M, Lareu MV, Carracedo A, Salas A (2009) Testing the performance of mtSNP minisequencing in forensic samples. Forensic Sci Int Genet 3(4):261–264 Mosquera-Miguel A, Alvarez-Iglesias V, Cerezo M, Lareu MV, Carracedo A, Salas A (2009) Testing the performance of mtSNP minisequencing in forensic samples. Forensic Sci Int Genet 3(4):261–264
10.
Zurück zum Zitat Palencia-Madrid L, Cardoso S, Castro-Maestre F, Baroja-Careaga I, Rocandio AM, de Pancorbo MM (2019) Development of a new screening method to determine the main 52 mitochondrial haplogroups through a single minisequencing reaction. Mitochondrion 45:46–51CrossRef Palencia-Madrid L, Cardoso S, Castro-Maestre F, Baroja-Careaga I, Rocandio AM, de Pancorbo MM (2019) Development of a new screening method to determine the main 52 mitochondrial haplogroups through a single minisequencing reaction. Mitochondrion 45:46–51CrossRef
11.
Zurück zum Zitat Tamm E, Kivisild T, Reidla M, Metspalu M, Smith DG, Mulligan CJ, Bravi CM, Rickards O, Martinez-Labarga C, Khusnutdinova EK, Fedorova SA, Golubenko MV, Stepanov VA, Gubina MA, Zhadanov SI, Ossipova LP, Damba L, Voevoda MI, Dipierri JE, Villems R, Malhi RS (2007) Beringian standstill and spread of Native American founders. PLoS One 2(9):e829CrossRef Tamm E, Kivisild T, Reidla M, Metspalu M, Smith DG, Mulligan CJ, Bravi CM, Rickards O, Martinez-Labarga C, Khusnutdinova EK, Fedorova SA, Golubenko MV, Stepanov VA, Gubina MA, Zhadanov SI, Ossipova LP, Damba L, Voevoda MI, Dipierri JE, Villems R, Malhi RS (2007) Beringian standstill and spread of Native American founders. PLoS One 2(9):e829CrossRef
13.
Zurück zum Zitat Baeta M, Núñez C, Cardoso S, Palencia-Madrid L, Herrasti L, Etxeberria F, de Pancorbo MM (2015) Digging up the recent Spanish memory: genetic identification of human remains from mass graves of the Spanish Civil War and posterior dictatorship. Forensic Sci Int Genet 19:272–279CrossRef Baeta M, Núñez C, Cardoso S, Palencia-Madrid L, Herrasti L, Etxeberria F, de Pancorbo MM (2015) Digging up the recent Spanish memory: genetic identification of human remains from mass graves of the Spanish Civil War and posterior dictatorship. Forensic Sci Int Genet 19:272–279CrossRef
14.
Zurück zum Zitat Butler JM (2015) Advanced topics in forensic DNA typing: interpretation. Elsevier/Academic Press, Amsterdam [etc.] Butler JM (2015) Advanced topics in forensic DNA typing: interpretation. Elsevier/Academic Press, Amsterdam [etc.]
15.
Zurück zum Zitat Bregu J, Conklin D, Coronado E, Terrill M, Cotton RW, Grgicak CM (2013) Analytical thresholds and sensitivity: establishing RFU thresholds for forensic DNA analysis. J Forensic Sci 58(1):120–129CrossRef Bregu J, Conklin D, Coronado E, Terrill M, Cotton RW, Grgicak CM (2013) Analytical thresholds and sensitivity: establishing RFU thresholds for forensic DNA analysis. J Forensic Sci 58(1):120–129CrossRef
16.
Zurück zum Zitat Lipson M, Szécsényi-Nagy A, Mallick S, Pósa A, Stégmár B, Keerl V, Rohland N, Stewardson K, Ferry M, Michel M, Oppenheimer J, Broomandkhoshbacht N, Harney E, Nordenfelt S, Llamas B, Mende BG, Köhler K, Oross K, Bondár M, Marton T, Osztás A, Jakucs J, Paluch T, Horváth F, Csengeri P, Koós J, Sebők K, Anders A, Raczky P, Regenye J, Barna JP, Fábián S, Serlegi G, Toldi Z, Nagy EG, Dani J, Molnár E, Pálfi G, Márk L, Melegh B, Bánfai Z, Domboróczki L, Fernández-Eraso J, Mujika-Alustiza JA, Fernández CA, Echevarría JJ, Bollongino R, Orschiedt J, Schierhold K, Meller H, Cooper A, Burger J, Bánffy E, Alt KW, Lalueza-Fox C, Haak W, Reich D (2017) Parallel palaeogenomic transects reveal complex genetic history of early European farmers. Nature 551(7680):368–372CrossRef Lipson M, Szécsényi-Nagy A, Mallick S, Pósa A, Stégmár B, Keerl V, Rohland N, Stewardson K, Ferry M, Michel M, Oppenheimer J, Broomandkhoshbacht N, Harney E, Nordenfelt S, Llamas B, Mende BG, Köhler K, Oross K, Bondár M, Marton T, Osztás A, Jakucs J, Paluch T, Horváth F, Csengeri P, Koós J, Sebők K, Anders A, Raczky P, Regenye J, Barna JP, Fábián S, Serlegi G, Toldi Z, Nagy EG, Dani J, Molnár E, Pálfi G, Márk L, Melegh B, Bánfai Z, Domboróczki L, Fernández-Eraso J, Mujika-Alustiza JA, Fernández CA, Echevarría JJ, Bollongino R, Orschiedt J, Schierhold K, Meller H, Cooper A, Burger J, Bánffy E, Alt KW, Lalueza-Fox C, Haak W, Reich D (2017) Parallel palaeogenomic transects reveal complex genetic history of early European farmers. Nature 551(7680):368–372CrossRef
17.
Zurück zum Zitat Torroni A, Lott MT, Cabell MF, Chen YS, Lavergne L, Wallace DC (1994) mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region. Am J Hum Genet 55(4):760–776PubMedPubMedCentral Torroni A, Lott MT, Cabell MF, Chen YS, Lavergne L, Wallace DC (1994) mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region. Am J Hum Genet 55(4):760–776PubMedPubMedCentral
18.
Zurück zum Zitat A. Biosystems, (2005) GeneMapper (R) Software Version 4.0. Reference and Troubleshooting Guide A. Biosystems, (2005) GeneMapper (R) Software Version 4.0. Reference and Troubleshooting Guide
19.
Zurück zum Zitat Vallone PM, Just RS, Coble MD, Butler JM, Parsons TJ (2004) A multiplex allele-specific primer extension assay for forensically informative SNPs distributed throughout the mitochondrial genome. Int J Legal Med 118(3):147–157CrossRef Vallone PM, Just RS, Coble MD, Butler JM, Parsons TJ (2004) A multiplex allele-specific primer extension assay for forensically informative SNPs distributed throughout the mitochondrial genome. Int J Legal Med 118(3):147–157CrossRef
20.
Zurück zum Zitat Poetsch M, Blöhm R, Harder M, Inoue H, von Wurmb-Schwark N, Freitag-Wolf S (2013) Prediction of people’s origin from degraded DNA--presentation of SNP assays and calculation of probability. Int J Legal Med 127(2):347–357CrossRef Poetsch M, Blöhm R, Harder M, Inoue H, von Wurmb-Schwark N, Freitag-Wolf S (2013) Prediction of people’s origin from degraded DNA--presentation of SNP assays and calculation of probability. Int J Legal Med 127(2):347–357CrossRef
21.
Zurück zum Zitat Chaitanya L, van Oven M, Weiler N, Harteveld J, Wirken L, Sijen T, de Knijff P, Kayser M (2014) Developmental validation of mitochondrial DNA genotyping assays for adept matrilineal inference of biogeographic ancestry at a continental level. Forensic Sci Int Genet 11:39–51CrossRef Chaitanya L, van Oven M, Weiler N, Harteveld J, Wirken L, Sijen T, de Knijff P, Kayser M (2014) Developmental validation of mitochondrial DNA genotyping assays for adept matrilineal inference of biogeographic ancestry at a continental level. Forensic Sci Int Genet 11:39–51CrossRef
22.
Zurück zum Zitat Qiu C, Sanchez SE, Hevner K, Enquobahrie DA, Williams MA (2015) Placental mitochondrial DNA content and placental abruption: a pilot study. BMC Res Notes 8:447CrossRef Qiu C, Sanchez SE, Hevner K, Enquobahrie DA, Williams MA (2015) Placental mitochondrial DNA content and placental abruption: a pilot study. BMC Res Notes 8:447CrossRef
23.
Zurück zum Zitat Williams MA, Sanchez SE, Ananth CV, Hevner K, Qiu C, Enquobahrie DA (2013) Maternal blood mitochondrial DNA copy number and placental abruption risk: results from a preliminary study. Int J Mol Epidemiol Genet 4(2):120–127PubMedPubMedCentral Williams MA, Sanchez SE, Ananth CV, Hevner K, Qiu C, Enquobahrie DA (2013) Maternal blood mitochondrial DNA copy number and placental abruption risk: results from a preliminary study. Int J Mol Epidemiol Genet 4(2):120–127PubMedPubMedCentral
24.
Zurück zum Zitat Andréasson H, Nilsson M, Budowle B, Frisk S, Allen M (2006) Quantification of mtDNA mixtures in forensic evidence material using pyrosequencing. Int J Legal Med 120(6):383–390CrossRef Andréasson H, Nilsson M, Budowle B, Frisk S, Allen M (2006) Quantification of mtDNA mixtures in forensic evidence material using pyrosequencing. Int J Legal Med 120(6):383–390CrossRef
25.
Zurück zum Zitat Montesino M, Salas A, Crespillo M, Albarrán C, Alonso A, Alvarez-Iglesias V, Cano JA, Carvalho M, Corach D, Cruz C, Di Lonardo A, Espinheira R, Farfán MJ, Filippini S, García-Hirschfeld J, Hernández A, Lima G, López-Cubría CM, López-Soto M, Pagano S, Paredes M, Pinheiro MF, Rodríguez-Monge AM, Sala A, Sóñora S, Sumita DR, Vide MC, Whittle MR, Zurita A, Prieto L (2007) Analysis of body fluid mixtures by mtDNA sequencing: an inter-laboratory study of the GEP-ISFG working group. Forensic Sci Int 168(1):42–56CrossRef Montesino M, Salas A, Crespillo M, Albarrán C, Alonso A, Alvarez-Iglesias V, Cano JA, Carvalho M, Corach D, Cruz C, Di Lonardo A, Espinheira R, Farfán MJ, Filippini S, García-Hirschfeld J, Hernández A, Lima G, López-Cubría CM, López-Soto M, Pagano S, Paredes M, Pinheiro MF, Rodríguez-Monge AM, Sala A, Sóñora S, Sumita DR, Vide MC, Whittle MR, Zurita A, Prieto L (2007) Analysis of body fluid mixtures by mtDNA sequencing: an inter-laboratory study of the GEP-ISFG working group. Forensic Sci Int 168(1):42–56CrossRef
26.
Zurück zum Zitat Naue J, Sänger T, Schmidt U, Klein R, Lutz-Bonengel S (2011) Factors affecting the detection and quantification of mitochondrial point heteroplasmy using Sanger sequencing and SNaPshot minisequencing. Int J Legal Med 125(3):427–436CrossRef Naue J, Sänger T, Schmidt U, Klein R, Lutz-Bonengel S (2011) Factors affecting the detection and quantification of mitochondrial point heteroplasmy using Sanger sequencing and SNaPshot minisequencing. Int J Legal Med 125(3):427–436CrossRef
27.
Zurück zum Zitat Torroni A, Achilli A, Macaulay V, Richards M, Bandelt HJ (2006) Harvesting the fruit of the human mtDNA tree. Trends Genet 22(6):339–345CrossRef Torroni A, Achilli A, Macaulay V, Richards M, Bandelt HJ (2006) Harvesting the fruit of the human mtDNA tree. Trends Genet 22(6):339–345CrossRef
Metadaten
Titel
Validation of a 52-mtSNP minisequencing panel for haplogroup classification of forensic DNA samples
verfasst von
Leire Palencia-Madrid
Diana Vinueza-Espinosa
Miriam Baeta
Ana M. Rocandio
Marian M. de Pancorbo
Publikationsdatum
06.02.2020
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/s00414-020-02264-6

Weitere Artikel der Ausgabe 3/2020

International Journal of Legal Medicine 3/2020 Zur Ausgabe

Neu im Fachgebiet Rechtsmedizin

Molekularpathologische Untersuchungen im Wandel der Zeit

Open Access Biomarker Leitthema

Um auch an kleinen Gewebeproben zuverlässige und reproduzierbare Ergebnisse zu gewährleisten ist eine strenge Qualitätskontrolle in jedem Schritt des Arbeitsablaufs erforderlich. Eine nicht ordnungsgemäße Prüfung oder Behandlung des …

Vergleichende Pathologie in der onkologischen Forschung

Pathologie Leitthema

Die vergleichende experimentelle Pathologie („comparative experimental pathology“) ist ein Fachbereich an der Schnittstelle von Human- und Veterinärmedizin. Sie widmet sich der vergleichenden Erforschung von Gemeinsamkeiten und Unterschieden von …

Gastrointestinale Stromatumoren

Open Access GIST CME-Artikel

Gastrointestinale Stromatumoren (GIST) stellen seit über 20 Jahren ein Paradigma für die zielgerichtete Therapie mit Tyrosinkinaseinhibitoren dar. Eine elementare Voraussetzung für eine mögliche neoadjuvante oder adjuvante Behandlung bei …

Personalisierte Medizin in der Onkologie

Aufgrund des erheblichen technologischen Fortschritts in der molekularen und genetischen Diagnostik sowie zunehmender Erkenntnisse über die molekulare Pathogenese von Krankheiten hat in den letzten zwei Jahrzehnten ein grundlegender …