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Animal genetics1992; 23(1); 43-50;

Localization of the calcium release channel gene in cattle and horse by in situ hybridization: evidence of a conserved synteny with glucose phosphate isomerase.

Abstract: In situ hybridization techniques were used to localize regionally the calcium release channel (CRC) gene on cattle and horse chromosomes, using a porcine CRC cDNA probe. In cattle, the hybridization signal peaked on the 18q23-q26 bands and in horse on the 10pter region. Previous studies have shown that the glucose phosphate isomerase (GPI) gene localizes at the same site in both species, indicating that the two loci are syntenic. As CRC and GPI are syntenic in human, pig and mouse, the present results in cattle and horse represent another example of synteny conservation in the evolution of mammalian chromosomes.
Publication Date: 1992-01-01 PubMed ID: 1315127
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  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

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 article discusses how the calcium release channel gene in cattle and horse has been traced to specific regions on their chromosomes. The gene’s location aligns with that of the glucose phosphate isomerase gene in both species, providing further evidence of a conserved synteny – meaning the genes are located at the same position on the chromosomes – in mammalian evolution.

Methods and Findings

  • The researchers adopted in situ hybridization techniques to trace the calcium release channel (CRC) gene on the chromosomes of cattle and horses. They utilized a porcine CRC cDNA probe for their experiment.
  • The investigation found that the hybridization signal, which denotes the location of the CRC gene, was focused on the 18q23-q26 bands in cattle and the 10pter region in horses.

Comparison with Previous Studies

  • This study’s findings were compared with previous research noting that the glucose phosphate isomerase (GPI) gene is present at the same site in both species.
  • The GPI and CRC genes’ identical locations suggest they are syntenic, that is, they are found on the same sections of the chromosome in both species.

Implications for Evolution

  • This study’s findings contribute to prior knowledge indicating that the GPI and CRC genes are syntenic not only in cattle and horses but also in humans, pigs, and mice.
  • These instances of conserved synteny are significant as they provide evidence of common patterns in the organization and evolution of mammalian chromosomes.

Cite This Article

APA
Chowdhary BP, Harbitz I, Davies W, Gustavsson I. (1992). Localization of the calcium release channel gene in cattle and horse by in situ hybridization: evidence of a conserved synteny with glucose phosphate isomerase. Anim Genet, 23(1), 43-50.

Publication

ISSN: 0268-9146
NlmUniqueID: 8605704
Country: England
Language: English
Volume: 23
Issue: 1
Pages: 43-50

Researcher Affiliations

Chowdhary, B P
  • Department of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, Uppsala.
Harbitz, I
    Davies, W
      Gustavsson, I

        MeSH Terms

        • Animals
        • Calcium Channels / chemistry
        • Cattle / genetics
        • Chromosome Mapping
        • Genetic Linkage
        • Glucose-6-Phosphate Isomerase / genetics
        • Horses / genetics
        • Humans
        • Metaphase
        • Mice
        • Nucleic Acid Hybridization
        • Species Specificity
        • Swine

        Citations

        This article has been cited 6 times.
        1. Bowling AT, Breen M, Chowdhary BP, Hirota K, Lear T, Millon LV, Ponce de Leon FA, Raudsepp T, Stranzinger G. International system for cytogenetic nomenclature of the domestic horse. Report of the Third International Committee for the Standardization of the domestic horse karyotype, Davis, CA, USA, 1996.. Chromosome Res 1997 Nov;5(7):433-43.
          doi: 10.1023/a:1018408811881pubmed: 9421259google scholar: lookup
        2. Raudsepp T, Otte K, Rozell B, Chowdhary BP. FISH mapping of the IGF2 gene in horse and donkey-detection of homoeology with HSA11.. Mamm Genome 1997 Aug;8(8):569-72.
          doi: 10.1007/s003359900505pubmed: 9250862google scholar: lookup
        3. Breen M, Lindgren G, Binns MM, Norman J, Irvin Z, Bell K, Sandberg K, Ellegren H. Genetical and physical assignments of equine microsatellites--first integration of anchored markers in horse genome mapping.. Mamm Genome 1997 Apr;8(4):267-73.
          doi: 10.1007/s003359900407pubmed: 9096108google scholar: lookup
        4. Brzozowska A, Fries R, Womack JE, Grimholt U, Myklebost O, Rogne S. Isolation, sequencing, and expression analysis of a bovine apolipoprotein E (APOE) cDNA and chromosomal localization of the APOE locus.. Mamm Genome 1993;4(1):53-7.
          doi: 10.1007/BF00364665pubmed: 8422503google scholar: lookup
        5. Cockett NE, Jackson SP, Shay TL, Nielsen D, Moore SS, Steele MR, Barendse W, Green RD, Georges M. Chromosomal localization of the callipyge gene in sheep (Ovis aries) using bovine DNA markers.. Proc Natl Acad Sci U S A 1994 Apr 12;91(8):3019-23.
          doi: 10.1073/pnas.91.8.3019pubmed: 8159698google scholar: lookup
        6. Fries R, Eggen A, Womack JE. The bovine genome map.. Mamm Genome 1993;4(8):405-28.
          doi: 10.1007/BF00296815pubmed: 8104056google scholar: lookup