Evidence map›Paper›PMID 39482599›Full record

ArticleBMC ecology and evolution2024

Sequencing the orthologs of human autosomal forensic short tandem repeats provides individual- and species-level identification in African great apes.

Ettore Fedele, Jon H Wetton, Mark A Jobling

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Article in BMC ecology and evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Ettore FedeleDepartment of Genetics, Genomics & Cancer Sciences, University of Leicester, University Road, Leicester, LE1 7RH, UK.
Jon H WettonDepartment of Genetics, Genomics & Cancer Sciences, University of Leicester, University Road, Leicester, LE1 7RH, UK. jw418@le.ac.uk.
Mark A JoblingDepartment of Genetics, Genomics & Cancer Sciences, University of Leicester, University Road, Leicester, LE1 7RH, UK. maj4@le.ac.uk.

Funding

Natural Environment Research Council NE/L002493/1
6 · The paper itself

Abstract

backgroundGreat apes are a global conservation concern, with anthropogenic pressures threatening their survival. Genetic analysis can be used to assess the effects of reduced population sizes and the effectiveness of conservation measures. In humans, autosomal short tandem repeats (aSTRs) are widely used in population genetics and for forensic individual identification and kinship testing. Traditionally, genotyping is length-based via capillary electrophoresis (CE), but there is an increasing move to direct analysis by massively parallel sequencing (MPS). An example is the ForenSeq DNA Signature Prep Kit, which amplifies multiple loci including 27 aSTRs, prior to sequencing via Illumina technology. Here we assess the applicability of this human-based kit in African great apes. We ask whether cross-species genotyping of the orthologs of these loci can provide both individual and (sub)species identification.

resultsThe ForenSeq kit was used to amplify and sequence aSTRs in 52 individuals (14 chimpanzees; 4 bonobos; 16 western lowland, 6 eastern lowland, and 12 mountain gorillas). The orthologs of 24/27 human aSTRs amplified across species, and a core set of thirteen loci could be genotyped in all individuals. Genotypes were individually and (sub)species identifying. Both allelic diversity and the power to discriminate (sub)species were greater when considering STR sequences rather than allele lengths. Comparing human and African great-ape STR sequences with an orangutan outgroup showed general conservation of repeat types and allele size ranges. Variation in repeat array structures and a weak relationship with the known phylogeny suggests stochastic origins of mutations giving rise to diverse imperfect repeat arrays. Interruptions within long repeat arrays in African great apes do not appear to reduce allelic diversity.

conclusionsOrthologs of most human aSTRs in the ForenSeq DNA Signature Prep Kit can be analysed in African great apes. Primer redesign would reduce observed variability in amplification across some loci. MPS of the orthologs of human loci provides better resolution for both individual and (sub)species identification in great apes than standard CE-based approaches, and has the further advantage that there is no need to limit the number and size ranges of analysed loci.

Indexed as

HominidaeMicrosatellite RepeatsAnimalsForensic GeneticsGenotypeGorilla gorillaHigh-Throughput Nucleotide SequencingHumansPan paniscusSequence Analysis, DNABonoboChimpanzeeGorillaIndividual identificationMassively parallel sequencingShort-tandem repeat (STR)Single nucleotide polymorphism (SNP)Verogen ForenSeq™ DNA Signature Prep kit

Identifiers

PMID39482599
PMCPMC11526555

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.