[Immunochemical investigations on the gene expression of horse serum carboxylesterase (author’s transl)].
Abstract: Immunochemical and enzymatic analyses of horse serum carboxylesterase were carried out with respect to the existence of a silent gene. Sera with positive phenotypic expression of esterase, both heterozygotes and presumed homozygotes, were compared with:--sera with positive phenotypic expression but genotypically +/O;--sera with a negative phenotypic expression, i. e. genotypically O/O;--sera of natural +/O "hemi-zygotes": mules (donkey lacking the esterase);--positive sera heated at 60 degrees C;--positive sera after specific inhibition of enzymatic activity. Titration by immunocompetition has shown that sera phenotypically negative do not contain an immunologically active "dummy" protein; however, using a sensitive immunotitration (rocket immunoelectrophoresis), traces of active protein could be demonstrated. Sera of +/O genotypes, both horses and mules, contain approximatively half of esterase present in +/+ sera. Heating at 60 degrees destroys the antigenic properties of the esterase almost completely, while, on the contrary, a specific inhibition of enzymatic activity leaves the antigenic properties unaffected.
Publication Date: 1978-02-01 PubMed ID: 79331
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- English Abstract
- Journal Article
Summary
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The research article is about the immunochemical and enzymatic analysis of horse serum carboxylesterase to determine the presence of a silent gene.
Overview of the research
- The study examines the gene expression of horse serum carboxylesterase. Specifically, the research was looking for evidence of a silent gene – a gene that is present but not expressed in the phenotype.
- To conduct the research, the team compared different kinds of sera, including those with positive phenotypic expression of esterase – both assumed homozygotes and heterozygotes – against various other types of sera.
Research Findings
- The researchers used titration by immunocompetition, a technique used to determine the concentration of protein in a solution. They found that sera that are phenotypically negative do not contain an immunologically active dummy protein.
- However, a sensitive immunotitration method known as ‘rocket immunoelectrophoresis’ revealed the presence of some active protein traces.
- Horse and mule sera of +/O genotypes were found to have approximately half of the esterase present in +/+ sera. Esterase is an enzyme that splits esters into an acid and an alcohol in the process of hydrolysis.
- The study demonstrated that heating the serum at 60 degrees Celsius almost completely destroyed the antigenic properties of the esterase – meaning it could no longer trigger an immune response. However, specific inhibition of enzymatic activity did not impact the antigenic properties.
Significance of the Research
- This research provides valuable insights into the gene expression of horse serum carboxylesterase. Understanding these expressions and enzyme functions can potentially impact various fields such as veterinary medicine, genetics and possibly horse breeding strategies.
Cite This Article
APA
Méténier L, Kaminski M.
(1978).
[Immunochemical investigations on the gene expression of horse serum carboxylesterase (author’s transl)].
Ann Immunol (Paris), 129(2-3), 353-365.
Publication
Researcher Affiliations
MeSH Terms
- Animals
- Antigen-Antibody Reactions
- Carboxylic Ester Hydrolases / genetics
- Epitopes
- Genotype
- Horses / blood
- Immunoelectrophoresis
- Perissodactyla
- Phenotype
- Rabbits
Citations
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