Sex inversion as a model for the study of sex determination in vertebrates

As a consequence of genetic sex determination, the indifferent gonadal blastema normally becomes either a testis or an ovary. This applies to mammals and to the majority of non-mammalian vertebrates. With the exception of placental mammals, however, partial or complete sex inversion can be induced in one sex by sexual steroid hormones of the opposite sex during a sensitive period of gonadogenesis. There is evidence that also during normal gonadogenesis in these species, in the XY/XX mechanism of sex determination testicular differentiation is induced by androgens, and in the ZZ/ZW mechanism, ovarian differentiation by oestrogens. In either case, the hormones may act via serological H-Y antigen as a morphogenetic factor. In contrast, in placental mammals including man, primary gonadal differentiation is independent of sexual steroid hormones, and factors directing differential gonadal development have not yet been conclusively identified. However, various mutations at the chromosome or gene level, resulting respectively in sex inversion or intersexuality, have provided clues as to some genes involved and their possible nature. In this context also, serological H-Y antigen is discussed as a possible factor acting on primordial gonadal cells and inducing differential growth or morphogenesis or both. The data available at present allow a tentative outline of the genetics of sex determination in placental mammals.

Author(s):  
Huynh Minh Sang ◽  
Pham Xuan Ky ◽  
Ho Son Lam ◽  
Phan Minh Thu

Reproduction in teleosts is regulated by a series of hormones including gonadotropin-releasing hormones (GnRHs), gonadotropins (GTHs) and steroid hormones. To contribute better understanding of steroid hormones in reproduction and GnRH-a in gonadal maturation, this literature review is concerned with the changes of steroid hormone levels in relation with sex inversion, reproductive behavior and gonadal development as well as the application of GnRH-a for inducing maturation of marine fish. The results revealed that in many species of teleost, steroid hormones E2, 11-11-KT and DHP are abundantly produced in gonadal tissues under the control of pituitary gonadotropins, and are essential for critical steps of gametogenesis. Plasma steroid levels have been used as indicators for both of the sex of the fish and its stage in the seasonal reproductive cycle, particularly with regard to induction of spawning. Determination of plasma steroid levels in relation with the sexual status of the gonads over several reproductive seasons might provide valuable information on the mechanisms of sex inversion in ambisexual fish species. In addition, changes of plasma steroid levels in correlation with gonadal development, number of spawning, fecundity, were described clearly in many marine species. The review also indicated that exogenous administration of GnRH-a triggered for final maturation of brood stock of some teleosts. In summary E2, T, 11-KT and C21 steroids are in relation with sex inversion, reproductive processes and GnRH-a is successful for inducing gonadal maturation in some fish species.


1999 ◽  
Vol 87 (1-2) ◽  
pp. 175-180 ◽  
Author(s):  
N.A. Hanley ◽  
S.G. Ball ◽  
M. Clement-Jones ◽  
D.M. Hagan ◽  
T. Strachan ◽  
...  

Life Sciences ◽  
1994 ◽  
Vol 54 (21) ◽  
pp. PL363-PL367 ◽  
Author(s):  
Selva Rivas-Arancibia ◽  
Francisca Vazquez-Pereyra

Author(s):  
Mary Jane West-Eberhard

Distinctive male and female traits are perhaps the most familiar of all divergent specializations within species. In cross-sexual transfer, discrete traits that are expressed exclusively in one sex in an ancestral species appear in the opposite sex of descendants. An example is the expression of brood care by males in a lineage where ancestral females are the exclusive caretakers of the young, as in some voles (Thomas and Birney, 1979). Despite the prominence of sexual dimorphism and sex reversals in nature, and an early explicit treatment by Darwin, discussed in the next section, cross-sexual transfer is not often recognized as a major factor in the evolution of novelty (but see, on animals, Mayr, 1963, pp. 435-439; Mayr, 1970, p. 254; on plants, Iltis, 1983). When more widely investigated, cross-sexual transfer may prove to rival heterochrony and duplication as an important source of novelties in sexually dimorphic lineages. For this reason, I devote more attention here to cross-sexual transfer than to these other, well-established general patterns of change. The male and female of a sexually dimorphic species may be so different that it is easy to forget that each individual carries most or all of the genes necessary to produce the phenotype of the opposite sex. Sex determination, like caste determination and other switches between alternative phenotypes, depends on only a few genetic loci or, in many species, environmental factors (Bull, 1983). There is considerable flexibility in sex determination and facultative reversal in some taxa. Among fish, for example, there is even a species wherein sex is determined by juvenile size at a critical age (Francis and Barlow, 1993). The sex determination mechanism, whatever its nature, leads to a series of sex-limited responses, often coordinated by hormones and not necessarily all occurring at once. A distinguishing aspect of sexually dimorphic traits in adults is that there is often a close homology between the secondary sexual traits that are differently modified in the two sexes.


2015 ◽  
Vol 58 (3) ◽  
pp. 395-405 ◽  
Author(s):  
Amilton Cesar dos Santos ◽  
Diego Carvalho Viana ◽  
Gleidson Benevides de Oliveira ◽  
Luis Miguel Lobo ◽  
Antônio Chaves Assis-Neto

Author(s):  
Jason Ioannidis ◽  
Debiao Zhao ◽  
Michael J. McGrew ◽  
Michael Clinton

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