TriXY—Homogeneous genetic sexing of highly degraded forensic samples including hair shafts. (November 2016)

• Record Type: Journal Article
• Authors: Madel, Maria-Bernadette; Niederstätter, Harald; Parson, Walther
• Is Part Of: Forensic science international. Volume 25(2016:Nov.)
• Page Start: 166
• Page End: 174
• Publication Date: 2016-11
• Subjects: Real-time PCR -- High-resolution melting -- Sex determination -- Degraded DNA -- Ancient DNA -- Forensic science; Forensic genetics -- Periodicals; Génétique légale -- Périodiques; Forensic genetics; Electronic journals; Periodicals; 614.1
• DOI: 10.1016/j.fsigen.2016.09.001
• Languages: English
• ISSNs: 1872-4973

Abstract

Highlights: This study presents a new homogeneous PCR assay (high-resolution melting curve analysis) for robust sex diagnosis (TriXY), especially for the analysis of severely fragmented DNA. TriXY's closed-tube format avoids post-PCR sample manipulations and, therefore, distinctly reduces the risk of PCR product carry-over contamination and sample mix-up. The method is sensitive down to the DNA contents of approximately two diploid cells. TriXY outperforms existing sexing methods both in terms of sensitivity and minimum required template molecule lengths. Abstract: Sexing of biological evidence is an important aspect in forensic investigations. A routinely used molecular-genetic approach to this endeavour is the amelogenin sex test, which is integrated in most commercially available polymerase chain reaction (PCR) kits for human identification. However, this assay is not entirely effective in respect to highly degraded DNA samples. This study presents a homogeneous PCR assay for robust sex diagnosis, especially for the analysis of severely fragmented DNA. The introduced triplex for the X and Y chromosome (TriXY) is based on real-time PCR amplification of short intergenic sequences (<50 bp) on both gonosomes. Subsequent PCR product examination and molecular-genetic sex-assignment rely on high-resolution melting (HRM) curve analysis. TriXY was optimized using commercially available multi-donor human DNA preparations of either male or female origin and successfully evaluated on challenging samples, including 46 ancient DNA specimens from archaeological excavations and a total of 16 DNA samples extracted from different segments of eight hair shafts of male and female donors. Additionally, sensitivity and cross-species amplification were examined to further test the assay's utility in forensic investigations. TriXY's closed-tube format avoids post-PCR sample manipulations and, therefore, distinctly reduces the risk of PCR product carry-over contamination and sample mix-up, while reducing labour and financial expenses at the same time. The method is sensitive down to the DNA content of approximately two diploid cells and has proven highly useful on severely fragmented and low quantity ancient DNA samples. Furthermore, it even allowed for sexing of proximal hair shafts with very good results. In summary, TriXY facilitates highly sensitive, rapid, and costeffective genetic sex-determination. It outperforms existing sexing methods both in terms of sensitivity and minimum required template molecule lengths. Therefore, we feel confident that TriXY will prove to be a reliable addition to the toolbox currently used for sex-typing in forensic genetics and other fields of research.