Skip to main content
Log in

Variable spread of X inactivation affecting the expression of different epitopes of the Hya gene product in mouse B-cell clones

  • Original Articles
  • Published:
Immunogenetics Aims and scope Submit manuscript

Abstract

Cloned B-cell lines from a female T16H/XSxr mouse in which Tdy expression was suppressed due to X inactivation and from a male X/XSxr mouse, both of the (kxb)F1 haplotype, were examined for H-Y expression. This was determined both by their ability to act as targets for H-2k and H-2b-restricted H-Y-specific cytotoxic T cells and by their ability to stimulate the proliferation of H-2Kk, H-2Db (class I) and Ab (class II)-restricted T-cell clones. In B-cell clones from the T16H/XSxr mouse, expression of H-Y/Db exhibited partial X inactivation and only a proportion (≃ 30%) of the cells were targets for or stimulated H-2Db-restricted H-Y-specific T cells. In contrast, H-Y eiptopes restricted by H-2k (H-Y/Kk, H-Y/Dk) and Ab (H-Y/Ab) exhibited no X inactivation. Furthermore, no inactivation of H-Y/Db, H-Y/Ab, or H-Yk was observed in the male X/XSxr mouse. These results indicate that the T16H/XSxr female is a mosaic, as a result of the variable spread of X inactivation into the Sxr region. They further suggest that the H-Y antigen recognized in association with H-2k and H-2Db class I molecules and Ab class II molecules may be the product of more than one 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

  • Boon, T. and Van Pel, A.: T cell-recognized antigenic peptides derived from the cellular genome are not protein degradation products but can be generated directly by transcription and translation of short subgenic regions. A hypothesis. Immunogenetics 29: 75–79, 1989

    Google Scholar 

  • Brown, S. and Rastan, S.: Age-related reactivation of an X-linked gene close to the inactivation centre in the mouse. Genet Res 52: 151–154, 1988

    Google Scholar 

  • Cattanach, B. M.: Position effect variegation in the mouse. Genet Res 23: 291–306, 1974

    Google Scholar 

  • Cattanach, B. M., Pollard, C. E., and Hawkes, S. G.: Sex-reversed mice: XX and XO males. Cytogenetics 10: 318–337, 1971

    Google Scholar 

  • Cattanach, B. M., Evans, E. P., Burtenshaw, M., and Barlow, J.: Male, female and intersex development in mice of identical chromosome constitution. Nature 300: 445–446, 1982

    Google Scholar 

  • Feinberg, A. P. and Vogelstein, B.: A technique for radiolabelling DNA restriction endonuclease fragments to high specific activity. (Addendum.) Anal Biochem 137: 266–267, 1984

    CAS  PubMed  Google Scholar 

  • Lurquin, C., Van Pel, A., Mariame, B., De Plaen, E., Szikova, J.-P., Janssens, C., Reddehase, M. J., Lejeune, J., and Boon, T.: Structure of the gene of Tum- transplantation antigen P91A: the mutated exon encodes a peptide recognised with Ld by cytolytic T cells. Cell 58: 293–303, 1989

    Google Scholar 

  • Lyon, M. F.: Gene action in the X chromosome of the mouse (Mus musculus L). Nature 190: 372–373, 1961

    CAS  Google Scholar 

  • Lyon, M. F., Searle, A. G., Ford, C. E., and Ohno, S.: A mouse translocation suppressing sex-linked variegation. Cytogenetics 3: 306–323, 1964

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Scott, D., McLaren, A., Dyson, J. et al. Variable spread of X inactivation affecting the expression of different epitopes of the Hya gene product in mouse B-cell clones. Immunogenetics 33, 54–61 (1991). https://doi.org/10.1007/BF00211696

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00211696

Keywords

Navigation