Adriana Castillo , Verónica Gomes , Humberto Ossa , Bibiana Ribeiro , Maria João Prata , Fernando Rondón , Filipa Simão , Leonor Gusmão
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引用次数: 0
Abstract
In Colombia, a country in the northwest corner of South America, populations are highly diverse due to the intercontinental admixture of Native Americans, European settlers, and enslaved Africans. While genetic diversity has been largely assessed based on autosomal markers, studies on mtDNA are much scarcer, allowing only a fragmentary view of the distribution of maternal lineages in the country. In this study the genetic diversity of maternal lineages in Colombian Andean populations was interrogated to infer whether the pattern of structuring was in line with the different colonization histories of the departments within the region. The ultimate goal was to establish a haplotype database for forensic purposes. In a total of 458 individuals born and residing in the departments of the Andean region, haplotypes of the total mtDNA control region were determined and assigned to the corresponding haplogroups. Across the 10 departments, haplotype diversities ranged between 0.9665 and 0.9967, and power of exclusion between 0.9208 and 0.9845. A component ascribed to be of Native American ancestry prevailed in all departments, where 89.27 % of haplotypes in the total sample belonged to mtDNA macro-haplogroups A2, B4, C1, and D. The remaining lineages were of Eurasian (6.65 %) or African (4.08 %) origin. Pairwise FST values showed signs of genetic differentiation, but still only reached statistical significance when Risaralda or Cundinamarca were compared with other populations. Principal component analysis showed that the population structure was mainly due to some differences in Native American substrates. The results obtained highlighted a heterogeneity within Andean populations that must be considered when developing mtDNA haplotype databases for forensic purposes. In this context, the use of specific databases is recommended for the departments of Risaralda and Cundinamarca, while the other departments can rely on a single haplotype frequency database.
期刊介绍:
Forensic Science International: Genetics is the premier journal in the field of Forensic Genetics. This branch of Forensic Science can be defined as the application of genetics to human and non-human material (in the sense of a science with the purpose of studying inherited characteristics for the analysis of inter- and intra-specific variations in populations) for the resolution of legal conflicts.
The scope of the journal includes:
Forensic applications of human polymorphism.
Testing of paternity and other family relationships, immigration cases, typing of biological stains and tissues from criminal casework, identification of human remains by DNA testing methodologies.
Description of human polymorphisms of forensic interest, with special interest in DNA polymorphisms.
Autosomal DNA polymorphisms, mini- and microsatellites (or short tandem repeats, STRs), single nucleotide polymorphisms (SNPs), X and Y chromosome polymorphisms, mtDNA polymorphisms, and any other type of DNA variation with potential forensic applications.
Non-human DNA polymorphisms for crime scene investigation.
Population genetics of human polymorphisms of forensic interest.
Population data, especially from DNA polymorphisms of interest for the solution of forensic problems.
DNA typing methodologies and strategies.
Biostatistical methods in forensic genetics.
Evaluation of DNA evidence in forensic problems (such as paternity or immigration cases, criminal casework, identification), classical and new statistical approaches.
Standards in forensic genetics.
Recommendations of regulatory bodies concerning methods, markers, interpretation or strategies or proposals for procedural or technical standards.
Quality control.
Quality control and quality assurance strategies, proficiency testing for DNA typing methodologies.
Criminal DNA databases.
Technical, legal and statistical issues.
General ethical and legal issues related to forensic genetics.