Analyze Diet
Animal blood groups and biochemical genetics1978; 9(4); 197-205; doi: 10.1111/j.1365-2052.1978.tb01437.x

The null allele in the horse esterase (Es) system detected by enzyme assay and rocket immunoelectrophoresis in heterozygous animals.

Abstract: The detection of the recessive null allele of horse serum esterase (Es) is possible in heterozygotes Es+/EsO which by starch gel electrophoresis appear like homozygotes Es+/Es+. Two methods are proposed, the titration of enzymatic activity of esterase and the immunochemical titration of esterase as antigen. These methods can be applied to solve the cases of suspect parentage or in population studies.
Publication Date: 1978-01-01 PubMed ID: 756141DOI: 10.1111/j.1365-2052.1978.tb01437.xGoogle Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research paper presents methods for identifying a specific recessive gene found in horse serum esterase that usually isn’t detectable in certain genetic combinations.

Identification of Null Allele in Horse Esterase

The research focuses primarily on identifying a unique characteristic found in the horse esterase (Es) gene system, called a null allele. Here are the primary aspects to understand:

  • A null allele is a variant of a gene that lacks the gene’s normal function due to changes in its genetic sequence. This anomaly is usually recessive.
  • The null allele under investigation relates to the horse serum esterase (Es), an enzyme primarily responsible for breaking down certain chemicals in the horse’s body.
  • The particular interest of this research is on the null allele in heterozygotes Es+/EsO. Heterozygotes usually carry two different versions of a gene. In this case, Es+/EsO means the horse has one functional esterase gene and one null esterase gene.
  • However, these heterozygotes appear identical to homozygotes Es+/Es+ on a starch gel electrophoresis (a common method for visualising proteins), making it challenging to identify the presence of the null allele.

Detection Methods for Null Allele

The paper proposes two alternative methods capable of correctly identifying the null allele in heterozygous horses:

  • The titration of enzymatic activity of esterase: This method basically measures the amount of enzyme activity in the horse’s serum. By determining the level of activity, experts can see if it aligns with the presence of one functional gene (heterozygous) or two functional genes (homozygous).
  • The immunochemical titration of esterase as antigen: This method requires using the immune response to the esterase protein to measure the amount present in the serum, which subsequently helps to identify if there is a null allele present.

Applications of the Research

The primary applications of this research can be seen in two main fields:

  • Resolving cases of suspect parentage: In scenarios where the parentage of a horse is in question, these methods could provide definitive results.
  • Population studies: For research work focused on genetic understanding of horse populations, this technique could provide critical insights.

Cite This Article

APA
Kaminski M. (1978). The null allele in the horse esterase (Es) system detected by enzyme assay and rocket immunoelectrophoresis in heterozygous animals. Anim Blood Groups Biochem Genet, 9(4), 197-205. https://doi.org/10.1111/j.1365-2052.1978.tb01437.x

Publication

ISSN: 0003-3480
NlmUniqueID: 0263344
Country: Netherlands
Language: English
Volume: 9
Issue: 4
Pages: 197-205

Researcher Affiliations

Kaminski, M

    MeSH Terms

    • Alleles
    • Animals
    • Antigens
    • Esterases / genetics
    • Esterases / immunology
    • Genetic Carrier Screening
    • Horses / genetics
    • Immunoelectrophoresis
    • Phenotype

    Citations

    This article has been cited 0 times.