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Topic:Genomics

Genomics in horses involves the study and analysis of the horse genome to understand genetic variations and their implications for equine health, performance, and breeding. This field encompasses the identification and mapping of genes associated with specific traits, diseases, and conditions in horses. Techniques such as whole-genome sequencing and genome-wide association studies (GWAS) are employed to explore genetic diversity and inheritance patterns among different horse breeds. Genomics provides insights into hereditary disorders, informs selective breeding practices, and aids in the development of personalized veterinary care. This page compiles peer-reviewed research studies and scholarly articles that explore the applications, methodologies, and findings of genomic research in equine science.
Characterization of two polymorphic horse microsatellites: HMS15 and HMS20.
Animal genetics    April 1, 1996   Volume 27, Issue 2 123 
Guérin G, Bertaud M.No abstract available
Four equine dinucleotide repeats at microsatellite loci UCDEQ5, UCDEQ14, UCDEQ46 and UCDEQ62.
Animal genetics    April 1, 1996   Volume 27, Issue 2 129 
Eggleston-Stott ML, DelValle A, Bowling AT, Bautista M, Zahorchak R, Malyj W.No abstract available
Zoo-FISH delineates conserved chromosomal segments in horse and man. Raudsepp T, Frönicke L, Scherthan H, Gustavsson I, Chowdhary BP.Human chromosome specific libraries (CSLs) were individually applied to equine metaphase chromosomes using the fluorescence in situ hybridization (FISH) technique. All CSLs, except Y, showed painting signals on one or several horse chromosomes. In total 43 conserved chromosomal segments were painted. Homoeology could not, however, be detected for some segments of the equine genome. This is most likely related to the very weak signals displayed by some libraries, rather than to the absence of similarity with the human genome. In spite of divergence from the human genome, dated 70-80 million yea...
Nucleotide sequence of exons 5 to 9 of the p53 tumour-suppressor gene of the horse (Equus caballus).
DNA sequence : the journal of DNA sequencing and mapping    January 1, 1996   Volume 6, Issue 3 185-187 doi: 10.3109/10425179609010208
Nasir L, Reid SW.An evolutionary conserved 1.3 kb fragment corresponding to the horse p53 tumour suppressor gene was PCR amplified, cloned and the nucleotide sequence determined. The p53 fragment encoded exons 5 to 9 and the intervening introns. The nucleotide sequence and the predicted aminoacid sequence showed a high level of homology with human and donkey p53 sequences.
Differences between Taylorella equigenitalis strains in their invasion of and replication in cultured cells.
Clinical and diagnostic laboratory immunology    January 1, 1996   Volume 3, Issue 1 47-50 doi: 10.1128/cdli.3.1.47-50.1996
Bleumink-Pluym NM, ter Laak EA, Houwers DJ, van der Zeijst BA.The ability of Taylorella equigenitalis, the causative agent of contagious equine metritis, to invade and replicate in equine derm cells was studied. The kinetics of invasion and replication were determined for four T. equigenitalis strains. On the basis of these experiments, a simpler assay in which the invasive as well as the replicative properties of a particular strain could be determined was developed. This assay was used to characterize 32 strains, which had previously been typed by field inversion gel electrophoresis of genomic restriction fragments. The invasiveness of T. equigenitalis...
Demonstration of three DRB loci in a domestic horse family.
Immunogenetics    January 1, 1996   Volume 44, Issue 6 441-445 doi: 10.1007/BF02602805
Fraser DG, Bailey E.Single-strand conformational polymorphism (SSCP) gel electrophoresis and DNA sequencing were used to characterize the second exon of the horse DRB homologue as well as to identify eight new DRB alleles. The SSCP gels presented a complex pattern, with phenotypes exhibiting between 4 and 13 bands. The DRB SSCP patterns were studied for two families (6 to 13 bands per pattern). For both families, the patterns showed simple Mendelian inheritance. The polymerase chain reaction products from two individuals possessing homozygous major histocompatibility complex (MHC) alleles by descent were cloned a...
Comparison of nucleic and amino acid sequences and phylogenetic analysis of the Gs protein of various equine arteritis virus isolates.
Virus genes    January 1, 1996   Volume 13, Issue 1 87-91 doi: 10.1007/BF00576983
Lepage N, St-Laurent G, Carman S, Archambault D.The genetic variation in equine arteritis virus (EAV) Gs protein encoding gene was investigated. Nucleic and deduced amino acid sequences from eight different EAV isolates (one European, two American and five Canadian isolates) were compared with those of the Bucyrus reference strain. Nucleotide and amino acid identities between these isolates and the Bucyrus reference strain ranged from 92.3 to 96.4%, and 93.2 to 95.5%, respectively. However, phylogenetic tree analysis and estimation of genetic distances based on the Gs protein encoding gene sequences showed that the European prototype Vienna...
Phylogenetic analysis of open reading frame 5 of field isolates of equine arteritis virus and identification of conserved and nonconserved regions in the GL envelope glycoprotein.
Virology    December 20, 1995   Volume 214, Issue 2 690-697 doi: 10.1006/viro.1995.0087
Balasuriya UB, Timoney PJ, McCollum WH, MacLachlan NJ.The variation and phylogenetic relationship of open reading frame 5 (ORF5) of 3 different laboratory strains of the original prototype Bucyrus strain of equine arteritis virus (EAV), the modified live virus vaccine (ARVAC, Fort Dodge Laboratories), and 18 field isolates of EAV from North America and Europe were determined by comparison of their gene sequences. The viruses differed from the published sequence by between 3 (99.6% homology) and 94 (87.8%) nucleotides and by between 3 (98.8%) and 24 (90.6%) amino acids. The field isolates differed from each other by between 2 (99.7%) and 110 (85.7...
DNA testing in the equine.
The Veterinary clinics of North America. Equine practice    December 1, 1995   Volume 11, Issue 3 525-542 doi: 10.1016/s0749-0739(17)30314-0
Malyj W.No abstract available
Cloning of a DNA repeat element from horse: DNA sequence and chromosomal localization.
Genome    December 1, 1995   Volume 38, Issue 6 1132-1138 doi: 10.1139/g95-150
Broad TE, Forrest JW, Lewis PE, Pearce PD, Phua SH, Pugh PA, Stewart-Scott IA.A DNA repeat element, revealed initially by digestion of horse DNA with TaqI, was cloned and characterized by Southern and in situ hybridization studies and nucleotide sequencing. The clone, e4/1, consisted of 32 tandem reiteration of a unit repeat of 21-22 bp, and produced multilocus DNA fingerprinting profiles that were useful for parentage analysis in horses. The tandem repeat element was shown by in situ hybridization to be localized in the centromeres of the acrocentric but not metacentric classes of horse chromosomes.
Families of tandemly repeated DNA elements from horse: cloning, nucleotide sequence, and organization.
Genome    December 1, 1995   Volume 38, Issue 6 1285-1289 doi: 10.1139/g95-169
Broad TE, Ede AJ, Forrest JW, Lewis PE, Phua SH, Pugh PA.DNA repeats, revealed initially by digestion of horse DNA with restriction enzymes, were cloned and characterized by cross-hybridization studies and nucleotide sequencing. The Sau-like family of tandem repeats contained two classes of repetitive elements with unit repeats of about 80 bp that shared no sequence similarity. Both unit repeats were present, frequently in tandem, in cloned segments of horse DNA of less than 600 bp. Evidence is presented, based on their ladderlike patterns of hybridization to horse DNA and their high level of similarity to published sequences of satellites from equi...
Genetics and disease in the horse.
Equine veterinary journal    November 1, 1995   Volume 27, Issue 6 400-401 doi: 10.1111/j.2042-3306.1995.tb04416.x
Gerber V, Bailey E.No abstract available
Amino acid sequence of HSP-1, a major protein of stallion seminal plasma: effect of glycosylation on its heparin- and gelatin-binding capabilities.
The Biochemical journal    September 1, 1995   Volume 310 ( Pt 2), Issue Pt 2 615-622 doi: 10.1042/bj3100615
Calvete JJ, Mann K, Schäfer W, Sanz L, Reinert M, Nessau S, Raida M, Töpfer-Petersen E.We report the complete amino acid sequence of HSP-1, a major protein isolated from stallion seminal plasma or acid extracts of ejaculated spermatozoa. The protein consists of 121 amino acids organized in two types of homologous repeats arranged in the pattern AA'BB'. Each of the 13-15-residue A-type repeats contains two O-linked oligosaccharide chains. The B-type repeats span 44-47 amino acids each, are not glycosylated, and have the consensus pattern of the gelatin-binding fibronectin type-II module. This domain also occurs in the major bovine seminal plasma heparin-binding proteins PDC-109 (...
An equine microsatellite repeat at the VIAS-H64 locus.
Animal genetics    August 1, 1995   Volume 26, Issue 4 282 doi: 10.1111/j.1365-2052.1995.tb03263.x
Ewen KR, Matthews ME.No abstract available
Mitochondrial DNA sequences of various species of the genus Equus with special reference to the phylogenetic relationship between Przewalskii’s wild horse and domestic horse.
Journal of molecular evolution    August 1, 1995   Volume 41, Issue 2 180-188 doi: 10.1007/BF00170671
Ishida N, Oyunsuren T, Mashima S, Mukoyama H, Saitou N.The noncoding region between tRNAPro and the large conserved sequence block is the most variable region in the mammalian mitochondrial DNA D-loop region. This variable region (ca. 270 bp) of four species of Equus, including Mongolian and Japanese native domestic horses as well as Przewalskii's (or Mongolian) wild horse, were sequenced. These data were compared with our recently published Thoroughbred horse mitochondrial DNA sequences. The evolutionary rate of this region among the four species of Equus was estimated to be 2-4 x 10(-8) per site per year. Phylogenetic trees of Equus species demo...
The DNA sequence of equine herpesvirus 2.
Journal of molecular biology    June 9, 1995   Volume 249, Issue 3 520-528 doi: 10.1006/jmbi.1995.0314
Telford EA, Watson MS, Aird HC, Perry J, Davison AJ.The complete DNA sequence of equine herpesvirus 2 (EHV-2) strain 86/67 was determined. The genome is 184,427 bp in size and has a base composition of 57.5% G + C. Unusually for a herpesvirus, about a third of the sequence distributed in several large blocks appears not to encode proteins. The 79 open reading frames that were identified as probably polypeptide-coding are predicted to encode 77 distinct proteins. Amino acid sequence comparisons confirmed that EHV-2 is a gamma-herpesvirus that is genetically collinear with herpesvirus saimiri (HVS; a gamma 2-herpesvirus) and Epstein-Barr virus (E...
Extensive mtDNA diversity in horses revealed by PCR-SSCP analysis.
Animal genetics    June 1, 1995   Volume 26, Issue 3 193-196 doi: 10.1111/j.1365-2052.1995.tb03162.x
Marklund S, Chaudhary R, Marklund L, Sandberg K, Andersson L.The hypervariable D-loop region of mitochondrial DNA (mtDNA) was amplified with the polymerase chain reaction using total horse DNA samples. Analysis of single strand conformation polymorphism (SSCP) of denatured amplification products was carried out by native polyacrylamide (8%) gel electrophoresis followed by silver staining. As many as 15 distinct SSCP variants were revealed when screening a total of 78 maternally unrelated horses representing five different breeds. All breeds showed a high degree of polymorphism and the estimated probability (PImt) that two maternally unrelated individual...
Comparative RAPD-PCR analysis of lungworms (Dictyocaulidae) from fallow deer, cattle, sheep, and horses.
Zentralblatt fur Veterinarmedizin. Reihe B. Journal of veterinary medicine. Series B    May 1, 1995   Volume 42, Issue 3 187-191 doi: 10.1111/j.1439-0450.1995.tb00699.x
Epe C, Bienioschek S, Rehbein S, Schnieder T.Genomic DNA isolated from the four Dictyocaulus species D. viviparus, D. eckerti, D. filaria and D. arnfieldi was compared by random amplified polymorphic DNA polymerase chain reaction (RAPD)-PCR to get additional information whether lungworms from fallow deer belong to a separate species (D. eckerti) or have to be regarded as an isolate of D. viviparus in wild ruminants. The resulting banding patterns of the electrophoresed PCR products were compared to assess the degree of genetic differences between the different lungworms. For the two D. viviparus isolates a similarity coefficient of 93.4%...
Sodium channel inactivation is impaired in equine hyperkalemic periodic paralysis.
Journal of neurophysiology    May 1, 1995   Volume 73, Issue 5 1892-1899 doi: 10.1152/jn.1995.73.5.1892
Cannon SC, Hayward LJ, Beech J, Brown RH.1. Equine hyperkalemic periodic paralysis (E-HPP) is a dominantly inherited disorder of muscle that causes recurrent episodes of stiffness (myotonia) and weakness in association with elevated serum K+. Affected horses carry a mutant allele of the skeletal muscle isoform of the Na channel alpha-subunit. To understand how this mutation may cause the disease phenotype, the functional defect in Na channel behavior was defined physiologically by recording unitary currents from cell-attached patches on normal and affected equine myotubes. 2. The presence of the mutation was confirmed in our cell lin...
Equine parentage testing by microsatellite locus at chromosome 1q2.1.
Animal genetics    April 1, 1995   Volume 26, Issue 2 123-124 doi: 10.1111/j.1365-2052.1995.tb02647.x
Sakagami M, Tozaki T, Mashima S, Hirota K, Mukoyama H.No abstract available
Delineating minimal protein domains and promoter elements for transcriptional activation by lentivirus Tat proteins.
Journal of virology    April 1, 1995   Volume 69, Issue 4 2605-2610 doi: 10.1128/JVI.69.4.2605-2610.1995
Southgate CD, Green MR.Lentivirus Tat proteins comprise a novel class of RNA-binding transcriptional activators that are essential for viral replication. In this study, we performed a series of protein fusion experiments to delineate the minimal protein domains and promoter elements required for Tat action. We show that a 15-amino-acid region of equine infectious anemia virus (EIAV) Tat protein, when fused to the GAL4 or LexA DNA binding domain, can activate transcription in appropriate promoter contexts. In the natural human immunodeficiency virus type 1 long terminal repeat, activation by Tat is dependent on multi...
Differences in a ribosomal DNA sequence of Strongylus species allows identification of single eggs.
International journal for parasitology    March 1, 1995   Volume 25, Issue 3 359-365 doi: 10.1016/0020-7519(94)00116-6
Campbell AJ, Gasser RB, Chilton NB.In the current study, molecular techniques were evaluated for the species identification of individual strongyle eggs. Adult worms of Strongylus edentatus, S. equinus and S. vulgaris were collected at necropsy from horses from Australia and the U.S.A. Genomic DNA was isolated and a ribosomal transcribed spacer (ITS-2) amplified and sequenced using polymerase chain reaction (PCR) techniques. The length of the ITS-2 sequence of S. edentatus, S. equinus and S. vulgaris ranged between 217 and 235 nucleotides. Extensive sequence analysis demonstrated a low degree (0-0.9%) of intraspecific variation...
Unusual D system inheritance in Anglo-Arab horse.
Animal genetics    February 1, 1995   Volume 26, Issue 1 53-54 doi: 10.1111/j.1365-2052.1995.tb02622.x
Kakoi H, Gawahara H, Miura N.An unusual D system phenogroup appeared in one family line of Anglo-Arab horse. This phenogroup probably originated from inheritance with an apparent absence of factors and was transmitted through successive generations.
A new GC allele in horses.
Hereditas    January 1, 1995   Volume 122, Issue 1 91-93 doi: 10.1111/j.1601-5223.1995.00091.x
Ouragh L, Juneja RK, Bengtsson S.No abstract available
Equine parentage testing and DNA technology–the route forward?
The British veterinary journal    January 1, 1995   Volume 151, Issue 1 1-3 doi: 10.1016/s0007-1935(05)80054-5
Knapp MR, Goelet P.No abstract available
The complete cDNA and deduced amino acid sequence of equine IgE.
Molecular immunology    January 1, 1995   Volume 32, Issue 1 1-8 doi: 10.1016/0161-5890(94)00143-o
Navarro P, Barbis DP, Antczak D, Butler JE.The cDNA from a transcript encoding the complete heavy chain of the equine immunoglobulin IgE has been cloned and sequenced. A fragment of the equine epsilon gene was amplified from cDNA using PCR and this fragment was then used to probe a horse cDNA library prepared from peripheral blood lymphocytes. A recombinant clone containing the cDNA encoding the complete horse epsilon chain and its associated V-D-J and leader, was subsequently isolated and sequenced. Comparison of the deduced amino acid sequence of equine IgE with the C epsilon heavy chains of other species indicates it to be most simi...
Nucleotide sequence of exons 5 to 9 of the p53 tumour-suppressor gene of the donkey (Equus asinus).
DNA sequence : the journal of DNA sequencing and mapping    January 1, 1995   Volume 6, Issue 1 61-63 doi: 10.3109/10425179509074702
Nasir L, Reid SW.The evolutionary conserved region of the equine homologue of the p53 gene from the donkey genome was PCR amplified and cloned. The 1380 bp fragment consisted of exons 5 to 9 and the intervening introns. The exonic and intronic DNA sequences showed a variable but high level of homology with previously published human sequences. The aminoacid sequences corresponding to the evolutionary conserved domains II, III, and V were identical to the human regions, whilst domain IV was 96% homologous.
The identification of polymorphic microsatellite loci in the horse and their use in thoroughbred parentage testing.
The British veterinary journal    January 1, 1995   Volume 151, Issue 1 9-15 doi: 10.1016/s0007-1935(05)80057-0
Binns MM, Holmes NG, Holliman A, Scott AM.Six new horse microsatellite loci were identified by sequencing M13 clones containing horse genomic inserts which gave positive signals when probed with a CA/GT repeat probe. Oligonucleotide primer pairs were synthesized for these loci and for two previously described horse microsatellites, HTG4 and HTG6. Polymerase chain reaction assays were then carried out on a panel of 20 different unrelated Thoroughbred horse DNAs. DNAs from eight cases of double covering which could not be solved by conventional blood typing were also examined. Several of the loci amplified were found to be polymorphic a...
The complete mitochondrial DNA sequence of the horse, Equus caballus: extensive heteroplasmy of the control region.
Gene    October 21, 1994   Volume 148, Issue 2 357-362 doi: 10.1016/0378-1119(94)90713-7
Xu X, Arnason U.The sequence of the mitochondrial (mt) DNA of the horse (Equus caballus) was determined. The length of the sequence presented is 16,660 bp. This figure, however, is not absolute due to pronounced heteroplasmy caused by variable numbers of the motif GTGCACCT in the control region of different molecules. Boundaries of the 13 peptide-coding genes were determined by the presence of start and stop codons, and by analogy with other eutherian mtDNAs. Three genes (COIII, NADH3 and NADH4) were not terminated by a stop codon. Comparison among the peptide-coding genes of the horse and eight other mammals...
Genetic Bit Analysis: a solid phase method for typing single nucleotide polymorphisms.
Nucleic acids research    October 11, 1994   Volume 22, Issue 20 4167-4175 doi: 10.1093/nar/22.20.4167
Nikiforov TT, Rendle RB, Goelet P, Rogers YH, Kotewicz ML, Anderson S, Trainor GL, Knapp MR.A new method for typing single nucleotide polymorphisms in DNA is described. In this method, specific fragments of genomic DNA containing the polymorphic site(s) are first amplified by the polymerase chain reaction (PCR) using one regular and one phosphorothioate-modified primer. The double-stranded PCR product is rendered single-stranded by treatment with the enzyme T7 gene 6 exonuclease, and captured onto individual wells of a 96 well polystyrene plate by hybridization to an immobilized oligonucleotide primer. This primer is designed to hybridize to the single-stranded target DNA immediately...
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