Three sex-determining (SD) genes, SRY (mammals), Dmy (medaka), and DM-W (Xenopus laevis), have been identified to date in vertebrates. However, how and why a new sex-determining gene appears remains unknown, as do the switching mechanisms of the master sex-determining gene. Here, we used positional cloning to search for the sex-determining gene in Oryzias luzonensis and found that Gsdf Y (gonadal soma derived growth factor on the Y chromosome) has replaced Dmy as the master sex-determining gene in this species. We found that Gsdf Y showed high expression specifically in males during sex differentiation. Furthermore, the presence of a genomic fragment that included Gsdf Y converts XX individuals into fertile XX males. Luciferase assays demonstrated that the upstream sequence of Gsdf Y contributes to the male-specific high expression. Gsdf is downstream of Dmy in the sex-determining cascade of O. latipes, suggesting that emergence of the Dmy-independent Gsdf allele led to the appearance of this novel sexdetermining gene in O. luzonensis. IN most vertebrates, sex is determined genetically. Mammals and birds with cytogenetically well-differentiated sex chromosomes have sex determination systems that differ between the taxonomic classes but not within them (Solari 1994). In mammals, for example, the sex-determining (SD) gene SRY/Sry on the Y chromosome has a universal role in sex determination (Gubbay et al. 1990;Sinclair et al. 1990;Koopman et al. 1991;Foster et al. 1992). By contrast, some fish groups, such as salmonids, sticklebacks, and Oryzias fishes, have sex chromosomes that differ among closely related species (Devlin and Nagahama 2002;Woram et al. 2003;Takehana et al. 2007a;Ross et al. 2009).A DM-domain gene, Dmy, was the first SD gene identified in a nonmammalian vertebrate, the fish medaka Oryzias latipes (Matsuda et al. 2002(Matsuda et al. , 2007. In this species, the term Y chromosome is employed to refer to a recombining chromosome that carries the male-determining gene Dmy, and X is used for the homologous chromosome; these are not a heteromorphic pair. This gene is conserved among all wild populations of O. latipes examined to date . The closely related species O. curvinotus also has Dmy on its Y chromosome, which is orthologous to the O. latipes Y chromosome (Matsuda et al. 2003). However, Dmy has not been detected in any other type of fish, including other Oryzias fishes (Kondo et al. 2003). Analysis of the Y-specific region of the O. latipes sex chromosome has demonstrated that Dmy arose from duplication of the autosomal Dmrt1 gene (Nanda et al. 2002;Kondo et al. 2006). This Dmrt1 duplication is estimated to have occurred within the last 10 million years in a common ancestor of O. latipes, O. curvinotus, and O. luzonensis. In O. luzonensis, however, no functional duplicated copy of Dmrt1 has been detected (Kondo et al. 2003) (Figure 5A).O. luzonensis possesses an XX-XY system, which is homologous to an autosomal linkage group (LG 12) and Uwa 1985). In the d-rR strain, the wild-type alle...
DMRT1, which is found in many vertebrates, exhibits testis-specific expression during the sexual differentiation period, suggesting a conserved function of DMRT1 in the testicular development of vertebrate gonads. However, functional analyses have been reported only in mammals. The current study focused on the Dmrt1 function in the teleost medaka, Oryzias latipes, which has an XX-XY sex determination system. Although medaka sex is determined by the presence or absence of the Y chromosome-specific gene Dmy, we demonstrated that in one Dmrt1 mutant line, which was found by screening a gene-driven mutagenesis library, XY mutants developed into normal females and laid eggs. Histological analyses of this mutant revealed that the XY mutant gonads first developed into the normal testis type. However, the gonads transdifferentiated into the ovary type. The mutant phenotype could be rescued by transgenesis of the Dmrt1 genomic region. These results show that Dmrt1 is essential to maintain testis differentiation after Dmy-triggered male differentiation pathway.
Chromosomal sex determination is widely used by vertebrates, however, only two genes have been identified as master sex-determining genes: SRY/Sry in mammals and DMY in the teleost medaka. Transfer of both genes into genetically female (XX) individuals can induce male development. However, transgenic strains have not been established in both cases because of infertility of the transgenic founders in mammals and low germline transmission rates in medaka. In this study, we used a BAC clone containing DMY in a 117 kb genomic region and two types of fluorescent marker to establish two DMY-transgenic medaka strains. In these strains, exogenous DMY is completely linked to a male phenotype and early gonadal development is not different from that of the wild-type strain. Sex-linkage analysis showed that the exogenous DMY was located on linkage group (LG) 23 in one strain and on LG 5 in the other strain, whereas the sex chromosome in medaka is on LG 1. Real-time PCR analysis indicated that these strains have multiple copies of DMY and higher DMY expression levels than the wild-type strain. These results showed that LGs 23 and 5 function as sex chromosomes in the two strains, respectively. This is not only the first example of the artificial generation of heritable sex chromosomes in vertebrates but also the first evidence showing plasticity of homomorphic sex chromosomes. This plasticity appears to be a characteristic of lower vertebrates and the underlying cause of frequent sex chromosome switching, recently reported in several fish and frog species.
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