Genetics in horses encompasses the study of hereditary traits and the genetic makeup that influences various characteristics and health conditions in equine populations. This field involves the analysis of genes and their functions, inheritance patterns, and the impact of genetic variations on traits such as coat color, performance ability, and susceptibility to diseases. Research in equine genetics employs techniques such as genome mapping, sequencing, and genetic testing to identify specific genes and mutations associated with these traits. This page gathers peer-reviewed research studies and scholarly articles that explore the genetic basis of equine traits, the methodologies used in genetic research, and the implications for breeding, health management, and conservation of horse breeds.
Tischner M, Kosiniak K, Bielański W.The emission of stallion semen was studied with the aid of
an `open' Krak\l=o'\w-72Model artificial vagina. The pattern of mating
behaviour was constant in all copulations observed : a mean number of
seven intravaginal thrusts was required to elicit ejaculation. The
pressure within the vestibule of the artificial vagina averaged 66 mmHg
at the beginning of copulation, 142 mmHg just before ejaculation, and
70 mmHg during the emission of semen. Emission appeared to be a more
variable process. Five to ten jets were observed; the mean number was
eight. The early jets occurred under high pr...
Oeding P, Hájek V, Marsálek E.Out of 70 S. aurew strains isolated from the anterior nares of horses, 48 (69 per cent)
belonged to the E biotype. Approximately one third of these isolates were typed with factor
sera, the 6 (35 per cent) that were typable showing 5 different patterns. All strains but one
were non-typable with the basic sets of phages for typing human and bovine staphylococci
even at RTD x 100. Without any exception the equine staphylococci of the E biotype
contained polysaccharide Aa. Sixteen biochemically different strains belonged to the biotype A, B or C. A number of different serological patterns an...
Swierstra EE, Gebauer MR, Pickett BW.The cycle of the seminiferous epithelium of the stallion was
divided into eight stages, using as criteria the presence of meiotic divi-
sions, shape of the spermatid nuclei and location of spermatids with
elongated nuclei in the tubule. The mean frequencies ofstages 1 to 8 were
16\m=.\9, 14\m=.\9, 3\m=.\2, 15\m=.\8, 7\m=.\4, 13\m=.\5, 12\m=.\6 and 15\m=.\7%, respectively. The
duration of one cycle of the seminiferous epithelium was 12\m=.\2 days
(S.E.\m=+-\0\m=.\1) as determined by injecting a single dose of 700 \g=m\Ciof
[3H]thymidine into each spermatic artery of six stallions and rem...
Jönsson L, Madsen P, Mark T.Genetic evaluations of sport performance typically consider competition records of ranking points in each competition, accumulated lifetime points or annual earnings. Repeated observations have the advantage of allowing for adjustment of effects associated with each competition such as rider experience, judge and competing horses, but also demands more computer capacity than single-trait records, which could prohibit multiple-trait evaluations. The aim of the study was to compare CPU times, estimated breeding values (EBVs), reliabilities and model prediction abilities when modelling repeated c...
Alstad AD, Sahu SP, Pedersen DD, Saari DA, Kawaoka Y, Webster RG.An influenza virus, A/equine/Alaska/1/91 (H3N8), was isolated from horses from Alaska with an acute respiratory infection. Pathogenic and serologic studies revealed that this virus is similar to previously isolated equine H3N8 influenza viruses. Antigenic analyses utilizing hemagglutination inhibition and neuraminidase inhibition assays indicated an antigenic drift from the prototype equine H3N8 influenza virus, A/equine/Miami/1/63. Partial sequence analysis of the A/equine/Alaska influenza virus indicated that each of 8 gene sequences are of equine origin.
Li GP, Seidel GE, Squires EL.Five experiments were designed to study the fertilizability and development of bovine oocytes fertilized by intracytoplasmic sperm injection (ICSI) with stallion spermatozoa. Experiment 1 determined the time required for pronuclear formation after ICSI. Equine sperm head decondensation began 3 h after ICSI; 42% were decondensed 6 h after ICSI. Male pronuclei (MPN) began to form 12 h after ICSI. Female pronuclei (FPN), however, formed as early as 6 h after ICSI. In Experiment 2, ionomycin, ionomycin plus 6-dimethylaminopurine (DMAP), and thimerosal were used to activate ICSI ova. None of the IC...
