Topic:Chromosomes
Chromosomes in horses are structures composed of DNA and proteins that carry genetic information crucial for the development, functioning, and reproduction of equine species. Horses typically have 64 chromosomes, organized into 32 pairs, which include one pair of sex chromosomes that determine the genetic sex of the individual. Chromosomal analysis in horses is used to study genetic disorders, inheritance patterns, and species evolution. Variations or abnormalities in chromosome number or structure can lead to developmental issues and impact fertility. This page compiles peer-reviewed research studies and scholarly articles that explore the structure, function, and implications of chromosomal variations in equine genetics and breeding.
A cytogenetic study of the Caspian pony. The group of Caspian ponies studied contained some animals with 65 chromosomes and others with 64 chromosomes. The morphology and G-banding pattern of the chromosomes resembled those of Equus caballus and E. przewalskii. The karyogram of animals with 65 chromosomes was identical to that of the cross between E. caballus and E. przewalskii. It is suggested that the Caspian pony is the product of natural hybridization between E. caballus and E. prezwalskii. Low reproductive effeciency of the Caspian pony is suggested as the cause of decline in the population of these animals.
Molecular cytogenetics of the Equidae. I. Purification and cytological localization of a (G + C)-rich satellite DNA from Equus przewalskii. A (G + C)-rich density satellite DNA (rho = 1.713 gm/cc) has been purified from splenic DNA of Przewalski's horse, Equus przewalskii, by successive equilibrium density gradient centrifugations. The purified satellite, which may comprise as much as 29% of the total DNA, renatures rapidly; however, analyses of native, single-stranded, and reassociated molecules by analytical ultracentrifugation and melting properties suggest that some sequence heterogeniety exists in the 1.713 gm/cc satellite. Complementary RNA (cRNA) transcribed from satellite DNA has been utilized for in situ hybridization stu...
Cytogenetic and clinical findings in mares with gonadal dysgenesis. Gonadal dysgenesis in the mare is associated with several different karyotypes, including sex chromosome aneuploidy (63,X; 63,X/64,XX; 63,X/64,XY or 65,XXX), the normal male complement (64,XY) and autosomal deletion (64,XX?del2q-). The 63,X is the most common karyotype found in gonadal dysgenesis. Aneuploid cases probably represent spontaneous chromosome non-disjunction during oogenesis, spermatogenesis or early embryonic development. Cases with XY or autosomal deletion may be inherited defects or of spontaneous origin.
Infertility in the horse associated with chromosomal abnormalities. Reproductive failure was studied in 12 phenotypically normal mares (9 Arabian, 3 Quarter horses, 1 Appaloosa and 1 pony). Karyotyping was performed using lymphocytes isolated from peripheral blood by density gradient procedures, followed by standard culture methods for karyotyping. Nine mares had karyotypes of 63,XO; 1 had 63,XO/64,XX; 1 had 63,XO/64,XY and 1 had 64,XY. All mares had small, firm ovaries that when removed and examined from 4 mares, lacked germ cells and consisted of undifferentiated ovarian stroma.
Horse, ass, and mule chromosomes. Karyotypes of the horse with 64 chromosomes, the ass with 62 chromosomes, and the mule with 63 chromosomes are presented. The chromosome complements of each species and their mule hybrid are analyzed and compared.
An equine cryptorchid with testicular and ovarian tissues. Cytogenetic and histological studies were carried out on an intersex horse which was diagnosed clinically as a cryptorchid. Surgery confirmed the horse to be a bilateral abdominal cryptorchid and histological examination revealed ovarian tissue associated with the left epididymis. Chromosome analysis of cultured cells from testicular tissue, ovarian tissue and skin revealed 64-XX and 64-XY make-up, the left gonad containing a greater preponderance of XX cells over XY cells. The external characteristics and behaviour of the horse were indistinguishable from that of a "routine" cryptorchid. Othe...
A male pseudohermaphrodite horse with 63Xo?/64XX/65XXY mixoploidy. This study investigates a case of intersexuality in a 6-month-old Arabian filly found to be a male pseudohermaphrodite. Genetic analysis reveals a peculiar chromosomal composition exhibiting mixoploidy – a rare […]
Male pseudohermaphroditism of the testicular feminizing type in a horse. Features characteristic of the hereditary syndrome of testicular feminization (tfm) were observed in a 7-year-old Quarter Horse. The horse had female body habitus and male psychosexual behaviour. Gonads located in the abdomen were testes and the uterus and cervix were absent. The vagina was normal in depth but ended as a blind pocket. The sex chromosome composition of testicular fibroblast and leucocyte cultures was XY. Construction of a family pedigree revealed a pattern of hereditary transmission similar to that reported for tfm in other mammalian species.
Gonadal dysgenesis in the mare. Five phenotypically normal but infertile mares were studied; four had karyotypes of 63XO, and one was a 25,64XX/13,63XO mosaic. The mares exhibited small uteri and has small ovaries that lacked germ cells and consisted primarily of undifferentiated ovarian stroma. These cases demonstrate that chromosome analysis is an important technique for the diagnosis of some forms of equine infertility.
The contribution of the mule to scientific thought. The infertility of the mule has proved a continuing challenge to scientific thought. Since the chromosomal differences between the two parental species are so great as to render normal meiosis impossible, it is postulated that all mules and hinnies are sterile. The problem now is to explain how mules and hinnies can occasionally produce spermatozoa or ova. The appearance of the mule was sufficient to persuade the ancients that both parents, not just the male, must contribute to the make-up of the offspring. The mule has also taught us that, when the number of oocytes in the ovary is reduced, t...
A review of cytogenetics in equine reproduction. The karyotype of the horse consists of 64 chromosomes; 18 pairs have a terminal centromere and 13 pairs a non-terminal centromere. Identification of individual chromosomes is enhanced by the use of band-staining techniques which allow recognition of minor structural rearrangements of chromatin material. Seven previously reported cases of male pseudohermaphroditism with chromosome studies are reviewed. Three were genetic females, one was basically an XX/XY chimaera, one was an XX/XXY chimaera, and one was an XXXY. Also reviewed is an infertile mare with 63 chromosomes and no distinguishable sex...
Chromosome abnormalities as a cause of infertility in mares. Chromosomal abnormalities have been detected in seven mares isolated by their poor reproductive performance. All had small or rudimentary gonads and absent or irregular oestrous cycles. Two mares had an XO genotype, one was a 65,XXX female and another a 64,XY sex-reversed female. Two other mares were sex chromosome mosaics of the 63,X/64,XX type. The seventh mare showed a normal female karyotype but a small extra autosomal fragment was found in a few cells.
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,...
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.
XO-gonadal dysgenesis in the mare (report of two cases). TWo cases of XO-gonadal dysgenesis in the mare are presented. Case No 1 was a pure 63, XO, while Case No 2 was a mosaic with a preponderance of XX cells. The clinical picture was one of phenotypically normal female mares with small uteri and infantile ovaries. The ovaries lacked germ cells, and consisted of stroma only. This study emphasizes the importance of chromosome analysis in providing information concerning the mechanisms involved is some cases of equine infertility.