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Animal blood groups and biochemical genetics1979; 10(4); 235-251; doi: 10.1111/j.1365-2052.1979.tb01031.x

Genetic polymorphism and close linkage of two alpha 1-protease inhibitors in horse serum.

Abstract: Two-dimensional electrophoretic analysis of horse serum proteins was done by a first-dimension separation in agarose gel (pH 5.4) followed by a second-dimension separation in horizontal polyacrylamide gel (pH 9.0). This method resulted in improved and reproducible separation of many alpha-globulins. Two groups of alpha 1-globulins, designated Pi1 and Pi2, were found to be protease inhibitors. Preliminary studies indicated that Pi1 and Pi2 proteins differed from each other in molecular weight and in protease inhibiting spectra. Extensive polymorphism was observed for both these proteins. Family data supported the hypothesis that Pi1 and Pi2 types were controlled by autosomal codominant alleles. For both Pi1 and Pi2 systems, most of the homozygous types showed two fractions each while the heterozygous types had 4 fractions. Six Pi1 and five Pi2 alleles were observed in two breeds of Swedish horses. Complete genetic linkage was observed for Pi1 and Pi2 loci as no recombinant type was observed in 40 informative matings studied.
Publication Date: 1979-01-01 PubMed ID: 94978DOI: 10.1111/j.1365-2052.1979.tb01031.xGoogle Scholar: Lookup
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  • Journal Article

Summary

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This research article discusses a study that investigated the genetic polymorphism and close linkage of two alpha 1-protease inhibitors in horse serum, identified as Pi1 and Pi2.

Methodology

  • The scientists used a two-dimensional electrophoretic analysis to examine horse serum proteins. They first separated the proteins in agarose gel at a pH of 5.4, and then again in a horizontal polyacrylamide gel at a pH of 9.0. This dual separation method led to improved and consistent separation of several alpha-globulins.

Findings

  • As part of the results, two groups of alpha 1-globulins were identified as Pi1 and Pi2, both of which showed protease inhibiting properties.
  • Initial studies revealed differences between Pi1 and Pi2 proteins in their molecular weight and protease inhibiting range. Both proteins underwent polymorphism.
  • Analysis of family data suggested that both Pi1 and Pi2 types were controlled by autosomal codominant alleles – a type of inheritance in which both inherited alleles contribute to the phenotype.
  • For both Pi1 and Pi2 systems, most of the homozygous types featured two factions, while the heterozygous types contained four factions.
  • In two breeds of Swedish horses, six Pi1 and five Pi2 alleles were observed.
  • The research found full genetic linkage between Pi1 and Pi2 loci, as no recombinant type was evident in the 40 informative matings set to study this aspect. This suggests that these loci might be very closely linked on the chromosome, or possibly even result from the same gene.

Significance

In conclusion, this study contributed valuable knowledge about the genetic polymorphism and linkage of protease inhibitors in horse serum. This information could potentially help other researchers understand more about the genetic underpinnings of certain equine diseases or conditions that involve these particular inhibitors. It could also inform animal breeding programs to maintain or improve equine health.

Cite This Article

APA
Juneja RK, Gahne B, Sandberg K. (1979). Genetic polymorphism and close linkage of two alpha 1-protease inhibitors in horse serum. Anim Blood Groups Biochem Genet, 10(4), 235-251. https://doi.org/10.1111/j.1365-2052.1979.tb01031.x

Publication

ISSN: 0003-3480
NlmUniqueID: 0263344
Country: Netherlands
Language: English
Volume: 10
Issue: 4
Pages: 235-251

Researcher Affiliations

Juneja, R K
    Gahne, B
      Sandberg, K

        MeSH Terms

        • Alleles
        • Alpha-Globulins / genetics
        • Animals
        • Crosses, Genetic
        • Gene Frequency
        • Genes
        • Genetic Linkage
        • Horses / genetics
        • Polymorphism, Genetic
        • Protease Inhibitors / genetics

        Citations

        This article has been cited 5 times.
        1. Braend M. Genetic variation of the equine serum protease inhibitor system Pi (Pr) characterized by an enzyme binding staining technique after starch gel electrophoresis. Acta Vet Scand 1982;23(4):592-602.
          doi: 10.1186/BF03546778pubmed: 6188351google scholar: lookup
        2. Patterson SD, Bell K. The equine protease inhibitory system (Pi): abnormal expressions of PiF, PiL, and PiS1. Biochem Genet 1986 Aug;24(7-8):529-43.
          doi: 10.1007/BF00504333pubmed: 3753429google scholar: lookup
        3. Gahne B, Juneja RK, Stratil A. Genetic polymorphism of human plasma alpha 1B-glycoprotein: phenotyping by immunoblotting or by a simple method of 2-D electrophoresis. Hum Genet 1987 Jun;76(2):111-5.
          doi: 10.1007/BF00284904pubmed: 3610142google scholar: lookup
        4. Potempa J, Wunderlich JK, Travis J. Comparative properties of three functionally different but structurally related serpin variants from horse plasma. Biochem J 1991 Mar 1;274 ( Pt 2)(Pt 2):465-71.
          doi: 10.1042/bj2740465pubmed: 2006910google scholar: lookup
        5. Patterson SD, Bell K, Shaw DC. The equine major plasma serpin multigene family: partial characterization including sequence of the reactive-site regions. Biochem Genet 1991 Oct;29(9-10):477-99.
          doi: 10.1007/BF02399689pubmed: 1772402google scholar: lookup