Sexual Differentiation of the Mullerian Ducts of the Chick Embryo

Nature ◽  
1962 ◽  
Vol 193 (4810) ◽  
pp. 88-89 ◽  
Author(s):  
TERRELL H. HAMILTON
PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e11945
Author(s):  
Lilja Fromme ◽  
Débora R. Yogui ◽  
Mario Henrique Alves ◽  
Arnaud L.J. Desbiez ◽  
Marion Langeheine ◽  
...  

Background The giant anteater belongs to the supraorder Xenarthra which occupies a systematically isolated position among placental mammals. The species is categorized as Vulnerable by the International Union for Conservation of Nature, and understanding its reproductive characteristics is critical for future conservation efforts. Methods Gross and microscopic anatomy of the genital organs of 23 male and 21 female adult and young roadkill giant anteaters in Brazil were studied. Results Male giant anteaters presented a short conical penis, intraabdominal testes, and prostate, vesicular and bulbourethral glands. A tubular remnant of the partially fused Müllerian ducts extended from the seminal colliculus through the prostate gland, continued cranially in the genital fold, bifurcated, and attached with one elongation each to the left and right epididymal corpus. The structure presented a total length of up to 10 cm and contained a yellowish liquid in its lumen. Histologically, the caudal section of this structure resembled the female vagina, the middle portion corresponded to the uterus, and the extensions showed characteristics of uterine tubes. In adult female giant anteaters, ovoid ovaries with occasional seminiferous cord-like structures were observed. The animals possessed a simple uterus, which was directly continuous with the vaginal canal. The caudal portion of the vagina had two lumina, separated by a longitudinal septum and opening into two apertures into the vaginal vestibule, cranial to the urethral opening. In the urethral and the lateral vestibular wall, glandular structures with characteristics of male prostate and bulbourethral glands, respectively, were found. The vestibule opened through a vertical vulvar cleft to the exterior. A pair of well-differentiated Wolffian ducts with a central lumen originated ventrally at the vaginal opening into the vestibule and passed in a cranial direction through the ventral vaginal and uterine wall. Each duct extended highly coiled along the ipsilateral uterine tube until the lateral pole of the ovaries where it merged with the rete ovarii. Discussion The reproductive morphology of giant anteaters reveals characteristics shared with other Xenarthrans: intraabdominal testes, a simple uterus, and a double caudal vagina. The persistence of well-differentiated genital ducts of the opposite sex in both males and females, however, singles them out among other species. These structures are the results of an aberration during fetal sexual differentiation and possess secretory functions. The possibility of a pathological degeneration of these organs should be considered in reproductive medicine of the species. Conclusion Knowledge of the unique reproductive characteristics of the giant anteater is essential for future reproductive management of the species. Additionally, further research on the peculiarities of the persisting genital duct structures might help to understand sexual differentiation in placental mammals in general.


Development ◽  
1978 ◽  
Vol 44 (1) ◽  
pp. 1-13
Author(s):  
Jean-Marie Gasc

The sex-dependent morphological asymmetry between gonads of bird embryos is generally considered to represent the critical point at which the definitive pattern of sexual differentiation is established. A quantitative study of growth in gonads of chick embryos (6- to 11-day-old) and of duck embryos (7- to 11-day-old) has been carried out in order to clarify in what manner growth of gonads is involved in sexual differentiation. Growth has been estimated by the determination of total protein and DNA content, and of DNA synthesis [3H]Tdr incorporation in vitro). Increase of protein and DNA content follow different growth curves according to the sex and the laterality of gonads. As early as day 6 (chick) or day 7 (duck) significant differences of protein content exist between gonads: left > right in both sex embryos, and male > female on both sides. Differences in DNA content of gonads are large even at the earliest stages. In the 6-day-old chick embryo both testes contain less DNA than the left ovary and more DNA than the right ovary. In the 7-day-old duck embryo both testes contain the same amount of DNA as the left ovary and twice as much DNA as the right ovary. Consequently, the protein/ DNA ratio has a different value according to the sex of the gonad. In the 6-day-old chick embryo and in the 7-day-old duck embryo absolute values of DNA synthesis (cpm/gonad) are higher in left gonads than in right gonads, and higher in male than in female gonads. When calculated as a ratio to the protein content (cpm/protein) DNA synthesis is lower in the left ovary than in the three other types of gonads, both in chick and duck embryos. When calculated as a ratio to the DNA content of gonads (cpm/DNA), DNA synthesis is lower in the left ovary than in the three other gonads in the chick, and lower in the left ovary and in testes than in the right ovary in the duck. The results show that growth of gonads is sex-dependent at a very early stage. The meaning of this sex character is discussed with special reference to the role of steroid hormone secretion.


2021 ◽  
Author(s):  
Abdol Hossain Ataei ◽  
Figen Kırkpınar

In intensive production, freshly hatched cockerels are culled in the layer hatchery (7 billion males each year), On the other hand, for meat production rearing female birds has not economic benefits because of male broiler chicks have a faster growth rate and better feed efficiency than females. In this regards several methods are being developed for sex determination in the chick embryo during the incubation period. But these methods need to be rapid, cost-efficient, and suitable practical for commercial use. Additionally, sex determination should be done before pain perception has evolved in chick embryos. Biotechnology by in ovo technique to sex determination of between male and female chicks or sex reversal could improve production and eliminate ethical dilemmas for poultry industries. In birds, the differentiation of embryonic gonads is not determined by genetic gender with the certainty that occurs in mammals and can be affected by early treatment with a steroid hormone. During the development of the chick embryo, the genotype of the zygote determines the nature of the gonads, which then caused male or female phenotype. The differentiation of gonads during the period called the "critical period of sexual differentiation" is accompanied by the beginning of secretion of sexual hormones. Namely, any change in the concentration of steroid hormones during the critical period affects the structure of the gonads. Many synthetic anti-aromatases such as federazole and non-synthetic in plants, mushrooms, and fruits containing natural flavonoids have been used in the experiments in ovo injection of anti-aromatase had no negative effect on the growth performance of sexual reversal female chickens. In conclusion, administration of an aromatase inhibitor causes testicular growth in the genetic female gender, and estrogen administration leads to the production of the left ovotestis in the genetic male gender. Therefore, in the early stages of embryonic development, sexual differentiation can be affected by changing the ratio of sexual hormones. In this review, effects of some substances applied by in ovo injection technique on sex reversal and performance in chicks.


1985 ◽  
Vol 6 (1) ◽  
pp. 83-92 ◽  
Author(s):  
Nicholas Mrosovsky ◽  
Jacques Fretey ◽  
Jean Lescure ◽  
Claude Pieau ◽  
Frédérique Rimblot

AbstractEggs of Dermochelys coriacea were incubated in the laboratory at different constant temperatures between 27 and 32°C up to hatching. The genital system of 72 neonates and 11 embryos was dissected and processed for histological study. All the individuals from the 27, 28 and 28.75°C incubations were phenotypic males. In the testes, the medulla was voluminous and very dense, composed of many epithelial cords, some enclosing germ cells, whereas the surface was covered by a thin layer of epithelial cells between which germ cells were still visible. The Müllerian ducts were in the process of regression. In all the individuals from eggs incubated at 29.75, 30.5 and 32°C, the gonads were somewhat longer than testes but were considerably reduced in width and thickness. The medulla was strongly inhibited, showing similar epithelial cords but much less numerous than in testes. The epithelium of the gonadal surface was pseudo-stratified and enclosed germ cells which had not enter meiotic prophase as in typical ovarian cortex. The Müllerian ducts were complete. These individuals were classified as potential females. These results show that temperature influences sexual differentiation of the gonads of Dermochelys coriacea and indicate that the threshold temperature (or pivotal temperature) lies between 28.75 and 29.75°C. They also reinforce fears about masculinising turtle populations by incubating eggs at cool temperatures in artificial hatcheries.


Author(s):  
J. J. Wang ◽  
C. S. Teng

The presence of SM-C/IGF-I has been described on chick embryo tissues. The binding of endogenous GH on Mullerian ducts (Mds) has been detected previously. Recently, the presence of SM/IGF and SM/IGF receptors were identified in 9-12 day-old mouse embryos. These evidences indicate that SM-C/IGF-I and GH are involved in embryonic development.Antiserum against porcine GH and anti-SM-C/IGF-I antibody were used as primary antibodies for immunocytochemical labelling probes by the avidin-biotin complex (ABC)-gold technique. There is no or very weak cross reactions between these two antibodies by ELISA. Chick embryos and Mds were fixed in 2.5% glutaraldehyde for 30 minutes. Washes with phosphate buffer were administered between each of the following incubations: 1. 2% bovine serum albumin, 2. Primary antibody (1/200 dilution), 3. Biotinated secondary antibody (1/100), 4. Avidin conjugated with gold particles (1/50). The 10-day Mds were double labelled with SM-C/IGF-I-gold and then with MIS-peroxidase (MIS-PO) as described before.


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