Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Mar 16;10(3):661.
doi: 10.3390/cells10030661.

Evolution of a Multiple Sex-Chromosome System by Three-Sequential Translocations among Potential Sex-Chromosomes in the Taiwanese Frog Odorrana swinhoana

Affiliations

Evolution of a Multiple Sex-Chromosome System by Three-Sequential Translocations among Potential Sex-Chromosomes in the Taiwanese Frog Odorrana swinhoana

Ikuo Miura et al. Cells. .

Abstract

Translocation between sex-chromosomes and autosomes generates multiple sex-chromosome systems. It happens unexpectedly, and therefore, the evolutionary meaning is not clear. The current study shows a multiple sex chromosome system comprising three different chromosome pairs in a Taiwanese brown frog (Odorrana swinhoana). The male-specific three translocations created a system of six sex-chromosomes, ♂X1Y1X2Y2X3Y3-♀X1X1X2X2X3X3. It is unique in that the translocations occurred among three out of the six members of potential sex-determining chromosomes, which are known to be involved in sex-chromosome turnover in frogs, and the two out of three include orthologs of the sex-determining genes in mammals, birds and fishes. This rare case suggests sex-specific, nonrandom translocations and thus provides a new viewpoint for the evolutionary meaning of the multiple sex chromosome system.

Keywords: autosome; fusion; hexavalent; sex-chromosome turnover.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest. The funders had no role in the design of the study.

Figures

Figure 1
Figure 1
Somatic and meiotic chromosomes of Odorrana swinhoana. Late replication banded karyotypes in male (a) and female (b). Chromosomes 1, 3, and 7 are heteromorphic in males (indicated by arrows), whereas they are homomorphic in females. The metaphase at first meiotic division comprises one hexavalent and ten bivalent rings (c). Each of the chromosome members comprising the hexavalent is numbered in red. The presumed pathway of triangular translocations through the chromosomes 1, 3 and 7 in male (d). The translocated chromosomal parts are diagrammatically indicated in black (chromosome 1), red (chromosome 3) and yellow (chromosome 7). The three translocations are diagrammatically represented in a box at the right bottom. Telomeres are indicated by two dots. The ring with an arrowhead indicates an inversion. Bar, 10 μm.
Figure 2
Figure 2
Chromosome painting and diagrams showing the multiple sex-chromosomes and potential sex-chromosomes. Hybridization with probes of microdissected chromosomes 1 (green) and 3 (red) onto the 1st meiotic chromosomes and somatic chromosomes of male and female (a1a3). Chromosome 1 probe DNA is shown in green, while chromosome 3, in red. The hybridization with hexavalent probe (red) onto the 1st meiotic chromosomes and somatic chromosomes of male and female (a4a6). Hexavalents are boxed by the white dotted line (a1,a4). Diagrams of six sex-chromosomes in males (left) and females (right) (b): chromosomal materials of No. 1, 3 and 7 are shown in black, red and yellow, respectively. The hexavalent is diagrammatically shown in (c). Thirteen haploid complements of ranid frogs, of which six potential sex-chromosomes are colored, and their chromosome numbers are circled (upper) (d). Orthologs of three sex-determining genes that are mapped in the Japanese frog G. rugosa are shown on the left or top of chromosomes 1 and 7, respectively. The late replication banding patterns of 13 chromosome complements are perfectly conserved between Glandirana rugosa and Odorrana swinhoana, shown at the bottom.

Similar articles

Cited by

References

    1. Graves J.A.M. The origin and function of the mammalian Y chromosome and Y-borne genes—An evolving understanding. BioEssays. 1995;17:311–320. doi: 10.1002/bies.950170407. - DOI - PubMed
    1. Graves J. Review: Sex chromosome evolution and the expression of sex-specific genes in the Placenta. Placenta. 2010;31:S27–S32. doi: 10.1016/j.placenta.2009.12.029. - DOI - PubMed
    1. Kitano J., Ross J.A., Mori S., Kume M., Jones F.C., Chan Y.F., Absher D.M., Grimwood J., Schmutz J., Myers R.M., et al. A role for a neo-sex chromosome in stickleback speciation. Nat. Cell Biol. 2009;461:1079–1083. doi: 10.1038/nature08441. - DOI - PMC - PubMed
    1. Smith D.A.S., Gordon I.J., Traut W., Herren J., Collins S., Martins D.J., Saitoti K., Ireri P., Ffrench-Constant R. A neo-W chromosome in a tropical butterfly links colour pattern, male-killing, and speciation. Proc. R. Soc. B Biol. Sci. 2016;283:20160821. doi: 10.1098/rspb.2016.0821. - DOI - PMC - PubMed
    1. Matsumoto T., Kitano J. The Intricate relationship between sexually antagonistic selection and the evolution of sex chro-mosome fusions. J. Theor. Biol. 2016;404:97–108. doi: 10.1016/j.jtbi.2016.05.036. - DOI - PubMed

Publication types

LinkOut - more resources