Skip to main content
Log in

A Single Genetic Determinant that Prevents Sex Reversal in C57BL-YPOS Congenic Mice

  • Published:
Biochemical Genetics Aims and scope Submit manuscript

Abstract

Sex determination in the mammalian embryo begins with the activation of a gene on the Y chromosome which triggers a cascade of events that lead to male development. The mechanism by which this gene, designated SRY in humans and Sry in mice (sex determining region of the Y chromosome), is activated remains unknown. Likewise, the downstream target genes for Sry remain unidentified at present. C57BL mice carrying a Y chromosome from Mus musculus musculus or molossinus develop normally as males. In contrast, C57BL/6 mice with the Y chromosome from M. m. domesticus often show sex reversal, i.e., develop as XY females. It has been documented that C57BL mice with the Y chromosome from Poschiavinus (YPOS), a domesticus subtype, always develop as females or hermaphrodites. This suggests that a C57BL gene either up- or downstream of Sry is ineffective in interacting with Sry, which then compromises the processes that lead to normal male sex development. Nonetheless, by selective breeding, we have been able to generate a sex reversal-resistant C57BL/6-congenic strain of mice in which the XYPOS individuals consistently develop as normal males with bilateral testes. Because the resistance to sex reversal was transferred from strain 129S1/Sv (nonalbino) by simple selection over 13 backcross generations, it is inferred that a single autosomal gene or chromosomal region confers resistance to the sex reversal that would otherwise result. XYPOS normal males generated in these crosses were compared to XYPOS abnormal individuals and to C57BL/6 controls for sexual phenotype, gonadal weight, serum testosterone, and major urinary protein (MUP) level. A clear correlation was found among phenotypic sex, MUP level, and testis weight in the males and in the incompletely masculinized XYPOS mice. The fully masculinized males of the congenic strain resemble C57BL/6 males in the tested parameters. DNA analysis confirmed that these males, in fact, carry the YPOS Sry gene.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

REFERENCES

  • Albrecht, K. H., and Eicher, E. M. (1997). DNA sequence analysis of the Sry alleles (subgenus Mus) implicates misregulation as the cause of C57BL/6J-YPOS sex reversal and defines the SRY functional unit. Genetics 147:1276.

    Google Scholar 

  • Berta, P., Hawkins, J. R., Sinclair, A. H., Taylor, A., Griffiths, B. L., Goodfellow, P. N., and Fellous, M. (1990). Genetic evidence equating SRY and the testis-determining factor. Nature 348:448.

    PubMed  Google Scholar 

  • Biddle, F. G., Eisner, J. R., and Eales, B. A. (1994). The testis-determining autosomal trait, Tda-1, of C57BL/6J is determined by more than a single autosomal gene when compared with DBA/2J mice. Genome 37:296.

    PubMed  Google Scholar 

  • Bocskei, Z., Groom, C. R., Flower, D. R., Wright, C. E., Phillips, S. E., Cavaggioni, A., Findlay, J. B., and North, A. C. (1992). Pheromone binding to two rodent urinary proteins revealed by X-ray crystallography. Nature 360:186.

    PubMed  Google Scholar 

  • Bowles, J., Cooper, L., Berkman, J., and Koopman, P. (1999). Sry requires a CAG repeat domain for male sex determination in Mus musculus. Nature Genet. 22:405.

    PubMed  Google Scholar 

  • Braun, A., Kammerer, S., Cleve, H., Lohrs, U., Schwarz, H. P., and Kuhnle, U. (1993). True hermaphroditism in a 46,XY individual, caused by a postzygotic somatic point mutation in the male gonadal sex-determining locus (SRY): Molecular genetics and histological findings in a sporadic case. Am.J.Hum.Genet. 52:578.

    PubMed  Google Scholar 

  • Coward, P., Nagai, K., Chen, D., Thomas, H. D., Nagamine, C. M., and Lau, Y. F. (1994). Polymorphism of a CAG trinucleotide repeat within Sry correlates with B6. YDom sex reversal. Nature Genet. 6:245.

    PubMed  Google Scholar 

  • Eicher, E. M. (1988). Autosomal genes involved in mammalian primary sex determination. Philos. Trans.R.Soc.Lond.Biol. 322:109.

    PubMed  Google Scholar 

  • Eicher, E. M. (1994). Sex and trinucleotide repeats. Nature Genet. 6:221.

    PubMed  Google Scholar 

  • Eicher, E. M., and Washburn, L. L. (1983). Inherited sex reversal in mice: Identification of a new primary sex-determining gene. J.Exp.Zool. 228:297.

    PubMed  Google Scholar 

  • Eicher, E. M., Washburn, L. L., Whitney, J. B., III, and Morrow, K. E. (1982). Mus poschiavinus Y chromosome in the C57BL/6 murine genome causes sex reversal. Science 217:535.

    PubMed  Google Scholar 

  • Eicher, E. M., Washburn, L. L., Schork, N. J., Lee, B. K., Shown, E. P., Xu, X., Dredge, R. D., Pringle, M. J., and Page, D. C. (1996). Sex-determining genes on mouse autosomes identified by linkage analysis of C57BL/6J-YPOS sex reversal. Nature Genet. 14(2):206.

    PubMed  Google Scholar 

  • Graves, P. E., and Erickson, R. P. (1995). Sequence variation in the 59, putative promoter of Sry and its possible relevance to the C57BL/6J-YDOM sex reversal. Biochem.Biophys.Res.Commun. 208:624.

    PubMed  Google Scholar 

  • Gubbay, J., Collignon, J., Koopman, P., Capel, B., Economou, A., Munsterberg, A., Vivian, N., Goodfellow, P., and Lovell-Badge, R. (1990). A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes. Nature 346:245.

    PubMed  Google Scholar 

  • Gubbay, J., Vivian, N., Economou, A., Jackson, D., Goodfellow, P., and Lovell-Badge, R. (1992). Inverted repeat structure of the Sry locus in mice. Proc.Natl.Acad.Sci.USA 89:7953.

    PubMed  Google Scholar 

  • Harley, V. R., Jackson, D. I., Hextall, P. J., Hawkins, J. R., Berkovitz, G. D., Sockanathan, S., Lovell-Badge, R., and Goodfellow, P. N. (1992). DNA binding activity of recombinant SRY from normal males and XY females. Science 255:453.

    PubMed  Google Scholar 

  • Hawkins, J. R., Koopman, P., and Berta, P. (1991). Testis-determining factor and Y-linked sex reversal. Curr.Opin.Genet.Dev. 1:30.

    PubMed  Google Scholar 

  • Hawkins, J. R., Taylor, A., Berta, P., Levilliers, J., Van der Auwera, B., and Goodfellow, P. N. (1992). Mutational analysis of SRY: Nonsense and missense mutations in XY sex reversal. Hum. Genet. 88:471.

    PubMed  Google Scholar 

  • Houle, A. M., and Taketo, T. (1992). True hermaphrodites: An experimental model in the mouse. J.Urol. 148:672.

    PubMed  Google Scholar 

  • Keel, B. A., and Abney, T. O. (1985). Oestrogen regulation of testicular androgen production during development in the rat. J.Endocrinol. 105:211.

    PubMed  Google Scholar 

  • Knopf, J. L., Gallagher, J. F., and Held, W. A. (1983). Differential, multihormonal regulation of the mouse major urinary protein gene family in the liver. Mol.Cell.Biol. 3:2232.

    PubMed  Google Scholar 

  • Koopman, P., Gubbay, J., Vivian, N., Goodfellow, P., and Lovell-Badge, R. (1991). Male development of chromosomally female mice transgenic for Sry. Nature 351:117.

    PubMed  Google Scholar 

  • Lau, Y.-F. C., and Zhang, J. (1998). Sry interactive proteins: Implications for the mechanisms of sex determination. Cytogenet.Cell.Genet. 80:128.

    PubMed  Google Scholar 

  • Lee, C. H., and Taketo, T. (1994). Normal onset, but prolonged expression, of Sry gene in the B6.YDOM sex-reversed mouse gonad. Dev.Biol. 1654:442.

    Google Scholar 

  • Mahadevaiah, S. K., Lovell-Badge, R., and Burgoyne, P. S. (1993). Tdy-negative XY, XXY and XYY female mice: Breeding data and synaptonemal complex analysis. J.Reprod.Fertil. 97:151.

    PubMed  Google Scholar 

  • Mannervik, M., Nibu, Y., Zhang, H., and Levine, M. (1999). Transcriptional coregulators in development. Science 284:606.

    PubMed  Google Scholar 

  • McElreavey, K., Barbaux, S., Ion, A., and Fellous, M. (1995). The genetic basis of murine and human sex determination: A review. Heredity 75:599.

    PubMed  Google Scholar 

  • Mucignat-Caretta, C., Carreta, A., and Cavaggioni, A. (1995). Acceleration of puberty onset in female mice by male urinary proteins. J.Physiol.(London) 486:517.

    Google Scholar 

  • Mucignat-Caretta, C., Carreta, A., and Baldini, E. (1998). Protein-bound male urinary pheromones: Differential responses according to age and gender. Chem.Senses 23:67.

    PubMed  Google Scholar 

  • Myers, R. B., and Abney, T. O. (1990). Testosterone and androstanediol production by regenerating Leydig cells in the ethylene dimethane sulphonate-treated mature rat. Int.J.Androl. 13:4.

    PubMed  Google Scholar 

  • Nagamini, C. M., Taketo, T., and Koo, G. C. (1987). Morphological development of the mouse gonad in tda-1 XY sex reversal. Differentiation 33:214.

    PubMed  Google Scholar 

  • Nallaseth, F. S. (1992). Sequence instability and functional inactivation of murine Y chromosomes can occur on a specific genetic background. Mol.Biol.Evol. 9(2):331.

    PubMed  Google Scholar 

  • Palmer, S. J., and Burgoyne, P. S. (1991). The Mus musculus domesticus Tdy allele acts later than the Mus musculus musculus Tdy allele: A basis for XY sex-reversal in C57BL/6-YPOS mice. Development 113:709.

    PubMed  Google Scholar 

  • Parker, K. L., Schedl, A., and Schimmer, B. P. (1999). Gene interactions in gonadal development. Annu.Rev.Physiol. 61:417.

    PubMed  Google Scholar 

  • Sinclair, A. H., Berta, P., Palmer, M. S., Hawkins, J. R., Griffiths, B. L., Smith, M. J., Foster, J. W., Frischauf, A. M., Lovell-Badge, R., and Goodfellow, P. N. (1990). A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif. Nature 346:240.

    PubMed  Google Scholar 

  • Taketo, T., Saeed, J., Nishioka, Y., and Donahoe, P. K. (1991). Delay of testicular differentiation in the B6.YDOM ovotestis demonstrated by immunocytochemical staining for mullerian inhibiting substance. Dev.Biol. 146:386.

    PubMed  Google Scholar 

  • Taketo-Hosotani, T., Nishioka, Y., Nagamine, C. M., Villalpando, I., and Merchant-Larios, H. (1989). Development and fertility of ovaries in the B6.YDOM sex-reversed female mouse. Development 107:95.

    PubMed  Google Scholar 

  • Washburn, L. L., and Eicher, E. M. (1989). Normal testis determination in the mouse depends on genetic interaction of a locus on chromosome 17 and the Y chromosome. Genetics 123:173.

    PubMed  Google Scholar 

  • Whitney, J. B., and Forrest, B. (1981). Hba: New genotypes. Mouse News Lett. 64:53.

    Google Scholar 

  • Whitney, J. B., and Russell, E. S. (1978). Alpha thalassemia (Hba th-J). Mouse News Lett. 58:47.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Whitney, J.B., Mills, T.M., Lewis, R.W. et al. A Single Genetic Determinant that Prevents Sex Reversal in C57BL-YPOS Congenic Mice. Biochem Genet 38, 119–137 (2000). https://doi.org/10.1023/A:1001935012134

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1001935012134

Navigation