"GenderPlex" a PCR multiplex for reliable gender determination of degraded human DNA samples and complex gender constellations

被引:30
作者
Codina, Anna Esteve [1 ]
Niederstaetter, Harald [1 ]
Parson, Walther [1 ]
机构
[1] Innsbruck Med Univ, Inst Legal Med, A-6020 Innsbruck, Austria
关键词
GenderPlex; PCR multiplex; Gender determination; Degraded human DNA samples; Complex gender constellations; AMELOGENIN GENE; RARE MUTATION; Y-CHROMOSOME; SHORT ARM; SEX TEST; REGION; IDENTIFICATION; DELETIONS; LOCUS; FAILURES;
D O I
10.1007/s00414-008-0301-z
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
The amelogenin test integrated in most commercial polymerase chain reaction (PCR) multiplex kits is routinely used in the forensic field for gender determination of DNA samples. It has been demonstrated that this test is not entirely reliable. Males with deletions in the homologous amelogenin part on the Y chromosome (AMELY) were erroneously typed as females due to lack of Y-specific amelogenin amplification. Also, primer binding site mutations that result in a failure to amplify the AMELY or the X-chromosomal part (AMELX) have been observed. For clarification of such phenomena, a new PCR multiplex (GenderPlex) is presented, co-amplifying two different regions of the amelogenin gene (55/58 and 106/112 bp for the AMELX and AMELY alleles, respectively), a 93-bp sequence stretch of the SRY gene and four mini-X-STR loci DXS7424, DXS8378, DXS6803 and GATA172D05 (maximum product size less than 140 bp). This strategy helps with the evaluation of samples for the presence of amelogenin-based primer site mutations and confirms a male genotype by the absence of heterozygote X-STR alleles and the presence of an SRY-related peak. The short amplicon sizes of all involved loci proved to be beneficial in a study on artificially degraded DNA. Furthermore, we demonstrate by means of sensitivity, human specificity and mixture studies that the multiplex is suitable for investigations in the forensic scene. Finally, the performance of the GenderPlex was evaluated on a west Eurasian population sample from Austria comprising 166 male and 104 female individuals.
引用
收藏
页码:459 / 464
页数:6
相关论文
共 40 条
[1]  
Alves C., 2006, PROGR FORENSIC GENET, V1288, P271, DOI DOI 10.1016/J.ICS.2005.10.036
[2]   MiniX-STR multiplex system population study in Japan and application to degraded DNA analysis [J].
Asamura, H ;
Sakai, H ;
Kobayashi, K ;
Ota, M ;
Fukushima, H .
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 2006, 120 (03) :174-181
[3]  
Ballard Linda Wood, 2002, J Biomol Tech, V13, P20
[4]   DNA recommendations - Further report of the DNA Commission of the ISFH regarding the use of short tandem repeat systems [J].
Bar, W ;
Brinkmann, B ;
Budowle, B ;
Carracedo, A ;
Gill, P ;
Lincoln, P ;
Mayr, W ;
Olaisen, B .
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 1997, 110 (04) :175-176
[5]   Dissection of mitochondrial superhaplogroup H using coding region SNPs [J].
Brandstatter, Anita ;
Salas, Antonio ;
Niederstatter, Harald ;
Gassner, Christoph ;
Carracedo, Angel ;
Parson, Walther .
ELECTROPHORESIS, 2006, 27 (13) :2541-2550
[6]  
BUEL E, 1995, J FORENSIC SCI, V40, P641
[7]   Male amelogenin dropouts: phylogenetic context, origins and implications [J].
Cadenas, A. M. ;
Regueiro, M. ;
Gayden, T. ;
Singh, N. ;
Zhivotovsky, L. A. ;
Underhill, P. A. ;
Herrera, R. J. .
FORENSIC SCIENCE INTERNATIONAL, 2007, 166 (2-3) :155-163
[8]   DXYS156:: a multi-purpose short tandem repeat locus for determination of sex, paternal and maternal geographic origins and DNA fingerprinting [J].
Calì, F ;
Forster, P ;
Kersting, C ;
Mirisola, MG ;
D'Anna, R ;
De Leo, G ;
Romano, V .
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 2002, 116 (03) :133-138
[9]  
Chang YM, 2003, J FORENSIC SCI, V48, P1309
[10]   A distinct Y-STR haplotype for Amelogenin negative males characterized by a large Yp11.2 (DYS458-MSY1-AMEL-Y) deletion [J].
Chang, Yuet Meng ;
Perumal, Revathi ;
Keat, Phoon Yoong ;
Yong, Rita Y. Y. ;
Kuehn, Daniel L. C. ;
Burgoyne, Leigh .
FORENSIC SCIENCE INTERNATIONAL, 2007, 166 (2-3) :115-120