Equine marker genes: polymorphism for plasminogen.
Abstract: Polymorphism for two autosomal alleles of equine plasminogen, PLG1 and PLG2, was demonstrated in plasma by isoelectric focusing and immunofixation, with a goat anti-human plasminogen antibody. The frequency of PLG2 was 0.16 in 150 Standardbreds, 0.20 in 96 Thoroughbreds, and 0.39 in 32 Shetland ponies. No evidence for linkage of PLG with any of 13 marker loci was found.
Publication Date: 1983-01-01 PubMed ID: 6197914DOI: 10.1111/j.1365-2052.1983.tb01075.xGoogle Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
- Research Support
- U.S. Gov't
- P.H.S.
Summary
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The research article is about the identification of polymorphism in two allelic forms of equine plasminogen, and its prevalence in different horse breeds, with no evidence for its linkage with any of 13 marker loci.
Study Overview
- The researchers conducted a study on equine plasminogen, an important protein involved in clotting and dissolution of clots, especially due to its key role in fibrinolysis or the breakdown of fibrin clots.
- The two versions of the gene that codes for plasminogen, termed PLG1 and PLG2, were identified as polymorphic, meaning that they exist in more than one form.
Methodology
- The scientists utilized isoelectric focusing and immunofixation, which are advanced techniques used in protein analysis. This was paired with a goat anti-human plasminogen antibody to detect the different versions of plasminogen in plasma samples taken from the horses.
- Isoelectric focusing allows for the separation of proteins based on their isoelectric point, or the pH at which a particular molecule or surface carries no net electrical charge. Immunofixation, on the other hand, uses antibodies to “fix” proteins, making them easier to identify and analyze.
Key Findings
- Frequency of PLG2 was determined to be 0.16 in 150 Standardbreds, 0.20 in 96 Thoroughbreds, and 0.39 in 32 Shetland ponies. This means that the presence of PLG2 version of the gene is different among various horse breeds.
- The study found no evidence for the linkage of plasminogen polymorphism with any of the 13 marker loci. This implies that the genetic variations observed in PLG1 and PLG2 are independent of these 13 marker loci, which means they are not physically close to or inherited together with these particular sets of markers on the chromosomes.
Implications
- This study provides important insights into the genetic diversity among different horse breeds, in particular, regarding the plasminogen gene.
- It could potentially be useful in understanding the genetic basis of certain diseases related to clotting and dissolution of clots. For example, genetic variation (polymorphism) in plasminogen could possibly influence the susceptibility of horses to certain clot-related diseases.
Cite This Article
APA
Weitkamp LR, Costello-Leary P, Guttormsen SA.
(1983).
Equine marker genes: polymorphism for plasminogen.
Anim Blood Groups Biochem Genet, 14(3), 219-223.
https://doi.org/10.1111/j.1365-2052.1983.tb01075.x Publication
Researcher Affiliations
MeSH Terms
- Alleles
- Animals
- Epitopes
- Gene Frequency
- Genetic Linkage
- Horses / genetics
- Isoelectric Point
- Plasminogen / genetics
- Plasminogen / immunology
Grant Funding
- 1R01 HD14487 / NICHD NIH HHS
Citations
This article has been cited 1 times.- Weitkamp LR, Guttormsen SA, Schultz JS. Linkage between the loci for the Lp(a) lipoprotein (LP) and plasminogen (PLG). Hum Genet 1988 May;79(1):80-2.
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