A mini-STR typing system for degraded equine DNA.
Abstract: Degraded biological samples are a challenge for testing laboratories. Genotyping success can be improved through the use of mini-STRs, by which primers are placed adjacent to the repeat motifs to reduce amplicon size. Here, we present a genetic profiling system comprising 13 autosomal and one X-linked dinucleotide-repeat markers and the SRY gene based on the internationally accepted equine parentage panel. The markers are divided into two panels with all alleles falling at or below 182 bp. The application of this method significantly increases the ability to profile difficult samples and to provide discriminating results to clients.
© 2018 Stichting International Foundation for Animal Genetics.
Publication Date: 2018-08-16 PubMed ID: 30117168DOI: 10.1111/age.12716Google Scholar: Lookup
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- Journal Article
Summary
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The research article discusses a new genetic profiling system designed to improve genotyping success in degraded biological samples, specifically equine DNA. The system utilizes mini-STRs and includes 13 autosomal, one X-linked dinucleotide-repeat markers, and the SRY gene.
Mini-STR Typing System
- This is the genetic profiling system proposed by the researchers. It is made to work effectively on degraded equine DNA samples.
- The system utilizes short tandem repeats (STRs). These are short sequences of DNA, normally of length 2-5 base pairs, that are repeated numerous times in a row.
- STR markers have high variation rates and are therefore very effective for DNA profiling.
- The term “mini-STR” specifically denotes smaller sized STRs, which are designed to be more effective on degraded or poor-quality DNA samples. Their smaller size allows for successful amplification where traditional STRs might fail.
Markers Included in the System
- The genetic profiling system presented includes 13 autosomal markers, one X-linked dinucleotide-repeat marker, and the SRY gene.
- Autosomal markers refer to DNA sequences that are found on any of the “autosomes” – the chromosomes that are not sex chromosomes. These play a crucial role in genetic profiling.
- The X-linked dinucleotide-repeat marker is a specific type of genetic marker linked to the X chromosome.
- The SRY gene is a sex-determining gene on the Y chromosome. It’s inclusion allows the profiling system to also determine the sex of the sample.
Overall Impact of the System
- The introduction and application of this mini-STR typing system greatly improve the ability to profile degraded biological samples, providing more precise and accurate results.
- These results might be critical in many areas such as forensics, evolutionary biology, genetic genealogy, and breeding and conservation strategies.
- Due to its effectiveness, it provides more discriminating and actionable results to clients, making it a valuable tool for laboratories tackling with challenging samples.
Cite This Article
APA
Kun TJ, Wictum EJ, Penedo MCT.
(2018).
A mini-STR typing system for degraded equine DNA.
Anim Genet, 49(5), 464-466.
https://doi.org/10.1111/age.12716 Publication
Researcher Affiliations
- Forensic Unit, School of Veterinary Medicine, University of California, Davis, CA, USA.
- Forensic Unit, School of Veterinary Medicine, University of California, Davis, CA, USA.
- Veterinary Genetics Laboratory, University of California, Davis, CA, USA.
MeSH Terms
- Animals
- Genes, sry
- Genotype
- Horses / genetics
- Microsatellite Repeats
- Sequence Analysis, DNA / veterinary
Grant Funding
- Veterinary Genetics Laboratory, UC Davis
Citations
This article has been cited 2 times.- Liu Y, Cui W, Jin X, Wang K, Mei S, Zheng X, Zhu B. Forensic Efficiency Estimation of a Homemade Six-Color Fluorescence Multiplex Panel and In-Depth Anatomy of the Population Genetic Architecture in Two Tibetan Groups. Front Genet 2022;13:880346.
- Tan Y, Tian H, Xiao Y, Xu B, Wang H, Yang M, Liu S. Screening a new set of microhaplotypes in exonic regions for sample identity testing and paternity testing during whole exome sequencing analysis. Int J Legal Med 2025 Jan;139(1):77-85.
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