Expressed gene sequences of the equine cytokines interleukin-17 and interleukin-23.
Abstract: This report describes the initial cloning and characterization of the equine interleukin-17 (IL-17) expressed gene sequence from mRNA obtained from equine intestinal tissue and interleukin-23 (IL-23) expressed gene sequence from mRNA obtained from equine peripheral blood mononuclear cells. Equine IL-17 has 462 nucleotides in the translated region, determined by homology with known human and mouse sequences, and shares 84% and 75% identity, respectively. For the deduced amino acid sequences, the identity with human and mouse is 76% and 70%. Equine IL-23 has 579 nucleotides in the translated region. Homology with known human and mouse sequences was determined to be 89% and 77%. Deduced amino acid identities are 89% with the human sequence and 70% with the mouse sequence. The gene sequences were identified as part of the U.S. Veterinary Immune Reagent Network with a goal of developing reagents in order to aid veterinary researchers in the investigation of diseases in livestock species.
Copyright 2009. Published by Elsevier B.V.
Publication Date: 2009-08-19 PubMed ID: 19775756DOI: 10.1016/j.vetimm.2009.08.008Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research focuses on the cloning and characterization of two types of equine cytokines, interleukin-17 and interleukin-23, obtained from horse intestinal tissue and peripheral blood mononuclear cells respectively.
Overview of the Study
- The study aims to examine the characteristics of the expressed gene sequences of two cytokines, named interleukin-17 (IL-17) and interleukin-23 (IL-23), in horses.
- These cytokines were obtained from two sources: equine intestinal tissue provided the IL-17, while IL-23 came from equine peripheral blood mononuclear cells.
Methods and Results
- The researchers initially cloned these equine cytokines and then studied their characteristics.
- The cloned equine IL-17 consists of 462 nucleotides in the translated region, sharing 84% and 75% identity with known human and mouse sequences, respectively.
- When considering the deduced amino acid sequences, the identity with human and mouse is slightly less, at 76% and 70% respectively.
- The equine IL-23 instead has 579 nucleotides in the translated region, and its identity was found to be 89% with human sequences and 77% with mouse sequences.
- Similar to IL-17, the deduced amino acid sequences identity of equine IL-23 with human and mouse sequences is 89% and 70%, respectively.
Purpose and Implications
- These gene sequences were identified as part of the U.S. Veterinary Immune Reagent Network’s initiative. The goal of this initiative is to develop reagents that could assist veterinary researchers to investigate diseases in livestock species.
- The identification and in-depth understanding of these cytokines could thus be a valuable contribution to veterinary medicine, aiding in the discovery of new treatments for diseases that afflict livestock.
Cite This Article
APA
Tompkins D, Hudgens E, Horohov D, Baldwin CL.
(2009).
Expressed gene sequences of the equine cytokines interleukin-17 and interleukin-23.
Vet Immunol Immunopathol, 133(2-4), 309-313.
https://doi.org/10.1016/j.vetimm.2009.08.008 Publication
Researcher Affiliations
- Department of Veterinary and Animal Sciences, Paige Laboratory, University of Massachusetts, Amherst, MA 01003, United States.
MeSH Terms
- Amino Acid Sequence
- Animals
- Base Sequence
- DNA Primers / genetics
- DNA, Complementary / genetics
- Gene Expression
- Horses / genetics
- Horses / immunology
- Humans
- Interleukin-17 / chemistry
- Interleukin-17 / genetics
- Interleukin-23 / chemistry
- Interleukin-23 / genetics
- Intestines / immunology
- Leukocytes, Mononuclear / immunology
- Mice
- Molecular Sequence Data
- Molecular Weight
- Phylogeny
- RNA, Messenger / genetics
- RNA, Messenger / metabolism
- Sequence Homology, Amino Acid
- Sequence Homology, Nucleic Acid
- Species Specificity
Citations
This article has been cited 1 times.- Ribitsch I, Baptista PM, Lange-Consiglio A, Melotti L, Patruno M, Jenner F, Schnabl-Feichter E, Dutton LC, Connolly DJ, van Steenbeek FG, Dudhia J, Penning LC. Large Animal Models in Regenerative Medicine and Tissue Engineering: To Do or Not to Do. Front Bioeng Biotechnol 2020;8:972.
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