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Topic:Genetics
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.
Spermatogenesis and duration of transit of spermatozoa through the excurrent ducts of stallions. The cycle of the seminiferous epithelium was divided into eight stages on the basis of meiotic divisions, shape of the spermatid nuclei and location of the spermatids with elongated nuclei. Duration of this cycle was 12-2 days (S.E. +/- 0-1) as determined by [3H]thymidine injections and autoradiography. The life-span of primary spermatocytes was 19-0 days, secondary spermatocytes 0-7 days, spermatids with round nuclei 8-7 days, and spermatids with elongated nuclei 10-1 days. Labelled spermatozoa entered the caput epididymidis 35 days, and appeared in the ejaculate 39-9 days, after the isotope ...
Cytogenetic studies of three equine hybrids. A detailed investigation of testicular meiosis in a mule, a hinny and a Przewalski horse/domestic horse hybrid were made. Abnormalities of pairing were observed in the mule and hinny in most germ cells at the pachytene stage of meiotic prophase, and spermatogenesis was alsmot totally arrested. A few mature spermatozoa were recovered from the ejaculate and epididymal flushings of the hinny. The Przewalski horse/domestic horse hybrid was fertile and showed normal spermatogenesis. Chromosome banding studies showed a close homology between the karyotypes of the Prezwalski horse (Equus przewalskii,...
A histochemical study of steroid metabolism in the equine fetus and placenta. The distribution of several hydroxysteroid dehydrogenases (HSD) was examined in a variety of equine placental and fetal tissues. The main points of interest were: (a) the lack of dehydrogenase activity in the gonad, (b) the appearance of a variety of HSDs in the trophoblast as early as 13 days of gestation, (c) the histochemical similarity between the cells of the trophoblast and the endometrial cup, and (d) the restriction of the strong endometrial 17beta-HSD reaction to those parts of the uterine epithelium directly apposed to the trophoblast.
[Production of antirickettsial sera by immunizing horses. II. Obtaining and testing an immune serum to D. sibericus]. The authors present the results of immunization of horses-producers with a commercial antigen and the yolk culture of the living R. sibericus (strain K1) for the purpose of obtaining specific immune sera for many purposes. It was shown that the original combined scheme of immunization and reimmunization of horses, successfully approved in the preparation of immune sera to Rickettsia prowazeki also proved to be highly effective for obtaining the antisera to R. sibericus. Sera obtained after the primary immunization of horses could be successfully used as diagnostic sera, but they were of no use...
An intersex (male pseudohermaphrodite) horse with 64XX/XXY mosaicism. The clinical, pathological and chromosomal findings in a male pseudohermaphrodite horse are reported. This animal appeared to be a female but showed strong male sexual behaviour. A small penis emerged from a rudimentary vagina. Two small testes were present in the abdomen and undifferentiated seminiferous tubules contained only supporting cells. No uterus was found. Culture of peripheral blood leucocytes revealed a 64XX/65XXY mosaicism.
Long chain base and fatty acid compositions of equine kidney sphingolipids. Equine renal glycopshingolipids were composed of galactocerebroside, glucocerbroside, ceramide dihexoside, ceramide trihexoside, sulfatide, globoside I, Forssman globoside, and hematoside. Free ceramide and sphingomyelin were also found in equine kidney. Their long chain bases consisted of sphingosine, dihydrosphingosine, C18-phytosphingosine, and C20-phytosphingosine, whereas the fatty acids were separated into two groups: nonhydroxy and hydroxy fatty acids. Ceramide monohexoside was separated into five spots by TLC on borax-impregnated plates. The major component of ceramide monohexoside was...
Immunological and chemical correlation between alpha-fetoproteins from human and several mammalian species. Alpha-Fetoproteins of several animals were purified and their molecular weights, amino acid compositions and peptide maps were compared, demonstrating the close similarities. These data indicated that the alpha-fetoproteins of mammalian species have closely related antigenical and chemical structures. Rabbits and horses were immunized with human alpha-fetoprotein, and it was observed that the animals produced antibodies reaction not only with human alpha-fetoprotein but with their homologous alpha-fetoproteins. The results were interpreted as the breakdown of the tolerance to their own alpha-f...
Conformational energy refinement of horse-heart ferricytochrome c. The reported X-ray structure of horse-heart ferricytochrome c has been refined by conformational energy calculations, using a three-stage computational procedure. In stage I, the atomic positions are adjusted to conform to idealized bond lengths and bond angles characteristic of small amino acid derivatives, while yet remaining as close as possible to the X-ray coordinates. In stage II, atomic overlaps are eliminated by adjusting the backbone and side-chain dihedral angles to minimize the nonbonded energy, hydrogen-bonded energy, and rotational energy contributions. In the final stage of refin...
The influence of amino acid substitutions on the conformational energy of cytochrome c. Conformational energies have been evaluated for each of the staggered side-chain conformations associated with the 261 amino acid substitutions known to occur among 60 eucaryotic species. At least 86% of these substitutions can be sterically accommodated (one at a time) within the structure of horse-heart cytochrome c resulting from conformational energy refinement. Simultaneous incorporation of all pertinent amino acid substitutions found in eight representative species into the refined horse-heart structure is also shown to be sterically possible, with few exceptions. In two cases (Pekin duc...
Studies on the epidemiology of Strongylus vulgaris infection of the horse. Studies on the epidemiology of Strongylus vulgaris infection of the
horse. International Journalfor Parasitology 5: 423426. Observations are reported on the size and age
structure of Stronglyus vulguris populations recovered from the anterior mesenteric artery and its
main branches of horses slaughtered at regular intervals throughout a year. Marked seasonal variations were found in the mean monthly numbers of worms present. During spring/early summer the
numbers were relatively low and a large proportion of the arteries had no worms in them at all.
Thereafter, the arterial worm burdens q...
Differences in subunit composition and iron content of isoferritins. Horse spleen ferritin was fractionated into its constituent isoferritins by isoelectric focusing. Separated isoferritins were stable and showed no tendency to redistribute when re-examined by analytical gel focusing. All of the isoferritins were immunologically indistinguishable when tested with antibodies raised against unfractionated horse spleen ferritin. The separated isoferritins also had similar conformations as determined by circular dichroism. Iron distribution studies, however, revealed a wide disparity among the isoferritins. The most acidic components had the lowest iron content but...
Inhibition of horse muscle acylphosphatase by pyridoxal 5′-phosphate. It has been shown that horse muscle acylphosphatase is inhibited by pyridoxal 5'-phosphate and that the inhibition is pH dependent, reversible and competitive with respect to substrate binding. Spectral analysis on the EI complex demonstrates the presence of a Schiff base. Reduction of the pyridoxal 5'-phosphate-inhibited enzyme with sodium borohydride, followed by amino acid analysis, produces a diminution of the free lysine peak and the appearance of a new peak corresponding to epsilon-pyridoxyllysine. The results suggest that there is at least one NH2-lysyl residue of horse muscle acylphosp...
Morphology of epididymal spermatozoa in the ass (Equus asinus) and stallion (Equus caballus). The morphological changes which take place in the sperm during their passage
through the excurrent ducts have been studied in the bull (BRANTON and SALISBURY
1947; HANCOCK 1955; BAILY and SMITH 1958; AMANN and ALMQUIST 1962; GUSTAFSSON and CRABO 1971 ; RAO 1971) and boar (GUSTAFSSON, CRABO and EINARSSON 1970).
Such knowledge is of major importance in understanding the origin and significance
of the different sperm abnormalties as well as providing the basis for proper appraisal
of semen picture and devising useful spermiograms.
The aim of the present work is to study the morphological ch...
Comparison of the myoglobin of the zebra (Equus burchelli) with that of the horse (Equus caballus). The tryptic and peptic peptides from the myoglobin of the zebra (Equus burchelli) have been compared with those obtained from the myoglobin of the horse (Equus caballus). No differences in the myoglobin were found between these two species.
Identification of O-cetylated N-acylneuraminic acids by mass spectrometry. A number of O-acetylated N-acylneuraminic acids, isolated from submandibular glands of cow and horse and from horse erythrocytes, have been characterized by mass spectrometry. On the basis of the typical fragmentation patterns of the pertrimethylsilyl derivatives of the methyl esters of the compounds, they were identified as 4-O-acetyl-, 9-O-acetyl-, 4,9-di-O-acetyl-, and 7,9-di-O-acetyl N-acetylneuraminic acid, and 4-O-acetyl-and 9-O-acetyl-N-glycolylneuraminic acid.
