Genetic insight into an extinct population of Asian elephants (Elephas maximus) in the Near East

The current range of the Asian elephant is fragmented and restricted to southern Asia. Its historical range was far wider and extended from Anatolia and the Levant to Central China. The fossil record from these peripheral populations is scant and we know little of their relationship to modern Asian elephants. To gain a first insight to the genetic affinity of an E. maximus population that once inhabited Turkey we sequenced ca. 570 bp mtDNA from four individuals dating to ~3500 cal. BP. We show that these elephants carried a rare haplotype previously only observed in one modern elephant from Thailand. These results clarify the taxonomic identity of specimens with indeterminate morphologies and show that this ancient population groups within extant genetic variation. By placing the age of the common ancestor of this haplotype in the interval 3.7–58.7 kya (mean = 23.5 kya) we show that range-wide connectivity occurred at some time or times since the start of MIS 3, ~57 kya, probably reflecting range and population expansion during a favourable climatic episode. The genetic data do not distinguish natural versus anthropogenic origin of the Near Eastern Bronze Age population, but together with archaeological and paleoclimatic data they allow the possibility of a natural westward expansion around that time

Elucidating recent history by tracing genetic affinity of three 16th century miners from Sweden.

Objectives: Sala Silver Mine in central Sweden was an important manufacturer of silver from at least the 16th till the early 20th century, with production peaking in the 16th, mid 17th and 19th centuries. The job opportunities offered by the mine attracted people to the area resulting in the development of a small township with an associated cemetery in the vicinity of the mining center. People affiliated to the mine were buried on the cemetery for around 150 years. Written sources reveal that common criminal convicts from Sweden-Finland and war prisoners from the numerous wars fought by Sweden during the time were exploited in the mine, and some of them were likely buried on the cemetery. The cemetery has been excavated on several occasions and the recovered human remains were divided into two different groups based on burial custom, demography and biochemical results. One group was believed to contain war prisoners; the aim of this study was to produce and interpret genomic data from these individuals to test if their genetic ancestry is consistent with the hypothesis that they were non-locals. Materials: Teeth from seven different individuals were sampled for dentine. Results: Three of the analyzed teeth contained sufficient amounts of endogenous human DNA for the generation of genomic sequence data to a coverage of 0.04, 0.19 and 0.83, respectively. Discussion: The results show that despite seeming heterogeneity the three individuals grouped within the range of genetic variation of modern and contemporary Swedes, yielding no statistical support to the hypothesis that they were foreign captives. However, due to the lack of contemporary or modern Danish genomic data we cannot refute these individuals originated in Denmark which was suggested as one of possible sources of the 17th century Swedish prisoners of war

Assessing the performance of quantity and quality metrics using the QIAGEN Investigator® Quantiplex® Pro RGQ kit

The Quantiplex® Pro RGQ kit quantifies DNA in a sample, supports the detection of mixtures and assesses the extent of DNA degradation based on relative ratios of amplified autosomal and male markers. Data show no significant difference in the accuracy and sensitivity of quantification between this and the Promega PowerQuant® System, both detecting the lowest amount of DNA tested, 4 pg. Laboratory controlled mixed male:female DNA samples together with mock sexual assault samples were quantified across a range of mixture ratios. Analysis software detected mixed DNA samples across all ratios for both quantification kits. Subsequent STR analysis using the Investigator® 24Plex QS Kit was able to corroborate mixture detection down to 1:25 male:female DNA ratios, past which point mixtures appeared identical to single-source female samples. Analysis software also detected laboratory degraded DNA samples, with data showing a positive trend between the Degradation Index (DI) and length of time of sonication. When used on ancient remains the assay was able to triage samples for further analysis, and STR profiles were concordant with DNA quantification results in all instances. STR analyses of laboratory-controlled sensitivity, mixture, and degradation studies supports the quality metric obtained from quantification. These data support the use of the Quantiplex® Pro RGQ kit for sample screening and quantification in forensic casework and ancient DNA studies