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Immunobiology1998; 199(1); 105-118; doi: 10.1016/s0171-2985(98)80067-3

Organization of the equine immunoglobulin heavy chain constant region genes; III. Alignment of c mu, c gamma, c epsilon and c alpha genes.

Abstract: Previous restriction analysis of cloned equine DNA and genomic DNA of equine peripheral blood mononuclear cells had indicated the existence of one c epsilon, one c alpha and up to six c gamma genes in the haploid equine genome. The c epsilon and c alpha genes have been aligned on a 30 kb DNA fragment in the order 5' c epsilon-c alpha 3'. Here we describe the alignment of the equine c mu and c gamma genes by deletion analysis of one IgM, four IgG and two equine light chain expressing heterohybridomas. This analysis establishes the existence of six c gamma genes per haploid genome. The genomic alignment of the cH-genes is 5' c mu/(/) c gamma 1/(/) c gamma 2/(/) c gamma 3/(/) c gamma 4/(/) c gamma 5/(/) c gamma 6/(/) c epsilon-c alpha 3', naming the c gamma genes according to their position relative to c mu. For three of the c gamma genes the corresponding IgG isotypes could be identified as IgGa for c gamma 1, IgG(T) for c gamma 3 and IgGb for c gamma 4.
Publication Date: 1998-08-26 PubMed ID: 9717671DOI: 10.1016/s0171-2985(98)80067-3Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research article explores the structure of equine immunoglobulin heavy chain constant region genes. The scientists specifically studied how the c mu, c gamma, c epsilon, and c alpha genes align in the equine, or horse, genome—finding that there are six c gamma genes per haploid genome, with the c gamma genes named according to their position relative to c mu.

Background

  • The study builds on prior research, which indicated the existence of one c epsilon, one c alpha, and up to six c gamma genes in the haploid equine genome.
  • Immunoglobulins are integral to an organism’s immune response, helping to fight infections. Studying the arrangement of these genes can contribute to advancements in equine health and disease resistance.

Methodology

  • The resources used included the cloned equine DNA and genomic DNA of equine peripheral blood mononuclear cells.
  • Deletions were systematically made in IgM, four IgG, and two equine light chain expressing heterohybridomas to uncover the alignment of the c mu and c gamma genes.

Findings

  • From their analysis, the researchers established the existence of six c gamma genes per haploid genome.
  • The genomic alignment of the cH-genes is the following sequence: 5′ c mu – c gamma 1 – c gamma 2 – c gamma 3 – c gamma 4 – c gamma 5 – c gamma 6 – c epsilon – c alpha 3′.
  • The c gamma genes are named according to their position relative to c mu.
  • The researchers also determined that IgGa corresponds to c gamma 1, IgG(T) corresponds to c gamma 3, and IgGb corresponds to c gamma 4.

Implications

  • The outcomes of this study provide more detailed understanding of the high-level structure of immunoglobulin heavy chain constant region genes in horses.
  • This discovery might inform future research studies or interventions to enhance equine health and immunological functioning.

Cite This Article

APA
Wagner B, Overesch G, Sheoran AS, Holmes MA, Richards C, Leibold W, Radbruch A. (1998). Organization of the equine immunoglobulin heavy chain constant region genes; III. Alignment of c mu, c gamma, c epsilon and c alpha genes. Immunobiology, 199(1), 105-118. https://doi.org/10.1016/s0171-2985(98)80067-3

Publication

ISSN: 0171-2985
NlmUniqueID: 8002742
Country: Netherlands
Language: English
Volume: 199
Issue: 1
Pages: 105-118

Researcher Affiliations

Wagner, B
  • Immunology Unit, Hannover School of Veterinary Medicine, Germany. bwagner@immunologie.tiho-hannover.de
Overesch, G
    Sheoran, A S
      Holmes, M A
        Richards, C
          Leibold, W
            Radbruch, A

              MeSH Terms

              • Animals
              • Bacterial Proteins
              • DNA Probes
              • Deoxyribonuclease BamHI
              • Deoxyribonucleases, Type II Site-Specific
              • Gene Deletion
              • Genes, Immunoglobulin
              • Horses / genetics
              • Horses / immunology
              • Hybridomas
              • Immunoglobulin Constant Regions / genetics
              • Immunoglobulin Heavy Chains / genetics
              • Immunoglobulin Switch Region / genetics
              • Polymorphism, Restriction Fragment Length
              • Restriction Mapping

              Citations

              This article has been cited 3 times.
              1. Al-Swailem AM, Shehata MM, Abu-Duhier FM, Al-Yamani EJ, Al-Busadah KA, Al-Arawi MS, Al-Khider AY, Al-Muhaimeed AN, Al-Qahtani FH, Manee MM, Al-Shomrani BM, Al-Qhtani SM, Al-Harthi AS, Akdemir KC, Inan MS, Otu HH. Sequencing, analysis, and annotation of expressed sequence tags for Camelus dromedarius. PLoS One 2010 May 19;5(5):e10720.
                doi: 10.1371/journal.pone.0010720pubmed: 20502665google scholar: lookup
              2. Wagner B, Greiser-Wilke I, Antczak DF. Characterization of the horse (Equus caballus) IGHA gene. Immunogenetics 2003 Nov;55(8):552-60.
                doi: 10.1007/s00251-003-0617-2pubmed: 14564492google scholar: lookup
              3. Keggan A, Freer H, Rollins A, Wagner B. Production of seven monoclonal equine immunoglobulins isotyped by multiplex analysis. Vet Immunol Immunopathol 2013 Jun 15;153(3-4):187-93.
                doi: 10.1016/j.vetimm.2013.02.010pubmed: 23541920google scholar: lookup