Skip to main content
Log in

Gtl2 lacZ, an insertional mutation on mouse Chromosome 12 with parental origin-dependent phenotype

  • Original Contributions
  • Published:
Mammalian Genome Aims and scope Submit manuscript

Abstract

We have produced a transgenic mouse line, Gtl2 lacZ (Gene trap locus 2), that carries an insertional mutation with a dominant modified pattern of inheritance:heterozygous Gtl2 lacZ mice that inherited the transgene from the father show a proportionate dwarfism phenotype, whereas the penetrance and expressivity of the phenotype is strongly reduced in Gtl2 lacZ mice that inherited the transgene from the mother. On a mixed genetic background this pattern of inheritance was reversible upon transmission of the transgene through the germ line of the opposite sex. On a predominantly 129/Sv genetic background, however, transgene passage through the female germ line modified the transgene effect, such that the penetrance of the mutation was drastically reduced and the phenotype was no longer obvious after subsequent male germ line transmission. Expression of the transgene, however, was neither affected by genetic background nor by parental legacy. Gtl2 lacZ maps to mouse Chromosome 12 in a region that displays imprinting effects associated with maternal and paternal disomy. Our results suggest that the transgene insertion in Gtl2 lucZ mice affects an endogenous gene(s) required for fetal and postnatal growth and that this gene(s) is predominantly paternally expressed.

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

  • Allen, N.D., Norris M.L., Surani, M.A. (1990). Epigenetic control of trans-gene expression and imprinting by genotype-specific modifiers. Cell 61, 853–861.

    Article  PubMed  CAS  Google Scholar 

  • Antonarakis, S.E., Blouin, J.-L., Maher, J., Avramopoulos, D., Thomas, G., Conover Talbot, J.C. (1993). Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14. Am. J. Hum. Genet. 52, 1145–1152.

    PubMed  CAS  Google Scholar 

  • Barlow, D.P., Stoger, R., Herrmann, B.G., Saito, K., Schweifer, N. (1991). The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the tme locus. Nature 349, 84–87.

    Article  PubMed  CAS  Google Scholar 

  • Bartolomei, M.S., Zemel, S., Tilghman, S.M. (1991). Parental imprinting of the mouse H19 gene. Nature 351, 153–155.

    Article  PubMed  CAS  Google Scholar 

  • Breen, M., Deakin, L., Macdonald, B., Miller, S., Sibson, R., Tartellin, E., Avner, P., Bourgade, F., Guénet, J.-L., Montagutelli, X., Poirier, C., Simon, D., Tailor, D., Bishop, M., Kelly, M., Rysavy, F., Rastan, S., Norris, D., Shepherd, D., Abbott, C, Pilz, A., Hodge, S., Jackson, I., Boyd, Y., Blair, H., Maslen, G., Todd, J.A., Reed, P.W., Stoye, J., Ashworth, A., McCarthy, L., Cox, R., Schalkwyk, L., Lehrach, H., Klose, J., Gangadharan, U. and Brown, S. (1994). Towards high regulation maps of the mouse and human genomes—a facility for ordering markers to 0.1 cM resolution. Hum. Mol. Genet. 3, 621–627.

    Article  CAS  Google Scholar 

  • Cattanach, B.M. and Beechy, C.V. (1990). Autosomal and X-chromosome imprinting. Development Suppl., 63–72.

  • Cattanach, B.M., Kirk, M. (1985). Differential activity of maternally and paternally derived chromosome regions in mice. Nature 315, 496–498.

    Article  PubMed  CAS  Google Scholar 

  • Cattanach, B.M., Rasberry, C. (1994). Evidence of imprinting involving the distal region of Chr. 12. Mouse Genome 91, 858.

    Google Scholar 

  • Chaillet, J.R., Bader, D.S., Leder, P. (1995). Regulation of genomic imprinting by gametic and embryonic processes. Genes Dev., 1177–1187.

  • Chaillet, J.R., Voght, T.F., Beier, D.R., Leder, P. (1991). Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis. Cell 66, 77–83.

    Article  PubMed  CAS  Google Scholar 

  • DeChiara, T.M., Robertson, E.J., Efstratiadis, A. (1991). Parental imprinting of the mouse insulin-like growth factor II gene. Cell 64, 849–859.

    Article  PubMed  CAS  Google Scholar 

  • DeLoia, J.A., Solter, D. (1990). A transgene insertional mutation at an imprinted locus in the mouse genome. Development Suppl. 73–79.

  • Efstratiadis, A. (1994). Parental imprinting of autosomal mammalian genes. Genes Dev. 4, 265–280.

    CAS  Google Scholar 

  • Engler, P., Haasch, D., Pinkert, C.A., Doglio, L., Glymour, M., Brinster, R., Storb, U. (1991). A strain-specific modifier on mouse chromosome 4 controls methylation of independent transgene loci. Cell 65, 939–947.

    Article  PubMed  CAS  Google Scholar 

  • Gossler, A., Zachgo, J. (1993). Gene and enhancer trap screens in ES cell chimaeras. In Gene Targeting: A Practical Approach, A. Joyner, ed. (Oxford: Oxford University Press), pp. 181–227.

    Google Scholar 

  • Gossler, A., Doetschman, T., Korn, R., Serfling, E., Kemler, R. (1986). Transgenesis by means of blastocyst-derived embryonic stem cell lines. Proc. Natl. Acad. Sci. USA 83, 9065–9069.

    Article  PubMed  CAS  Google Scholar 

  • Hadchouel, M., Farza, H., Simon, D., Tiollais, P., Pourcel, C. (1987). Maternal inhibition of hepatitis B surface antigen gene expression in transgenic mice correlates with de novo methylation. Nature 329, 454–456.

    Article  PubMed  CAS  Google Scholar 

  • Healey, S., Powell, F., Battersby, M., Chenevix-Trench, G., McGill, J. (1994). Distinct phenotype in maternal uniparental disomy of chromosome 14. Am. J. Med. Genet. 51, 147–149.

    Article  PubMed  CAS  Google Scholar 

  • Kratochwil, K., Von der Mark, K., Kollar, E.J., Jaenisch, R., Mooslehner, K., Schwarz, M., Haase, K., Gmachl, I., Harbers, K. (1989). Retrovirus-induced insertional mutation in Movl3 mice affects collagen I expression in a tissue specific manner. Cell 57, 807–816.

    Article  PubMed  CAS  Google Scholar 

  • Kratochwil, K., Ghaffaritabrizi, N., Holzinger, I., Harbers, K. (1993). Restricted expression of mov13 mutant alpha-1(i) collagen gene in osteo-blasts and its consequences for bone-development. Dev. Dyn. 198, 273–283.

    PubMed  CAS  Google Scholar 

  • Leff, S.E., Brannan, C.I., Reed, M.L., Ozcelik, T., Francke, U., Copeland, N.G., Jenkins, N.A. (1992). Maternal imprinting of the mousesnrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. Nature Genet. 2, 259–264.

    Article  PubMed  CAS  Google Scholar 

  • McGrath, J., Solter, D. (1984). Completion of mouse embryogenesis requires both the maternal and paternal genomes. Cell 37, 179–183.

    Article  PubMed  CAS  Google Scholar 

  • Reik, W. (1992). Genomic imprinting in mammals. Results Probl. Cell Differ. 18, 203–229.

    PubMed  CAS  Google Scholar 

  • Reik, W., Collick, A., Norris, M.L., Barton, S.C., Surrani, M.A. (1987). Genomic imprinting determines methylation of parental alleles in transgenic mice. Nature 328, 248–251.

    Article  PubMed  CAS  Google Scholar 

  • Reik, W., Howlett, S.K., Surani, A. (1990). Imprinting by DNA methylation: from transgenes to endogenous gene sequences. Development Suppl., 99–106.

  • Sambrook, J., Fritsch, E.F., Maniatis, T. (1989). Molecular Cloning: A Laboratory Manual, (Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory Press).

    Google Scholar 

  • Sapienza, C, Peterson, A.C., Rossant, J., Balling, R. (1987). Degree of methylation of transgenes is dependent on gamete of origin. Nature 328, 251–254.

    Article  PubMed  CAS  Google Scholar 

  • Schuster-Gossler, K., Zachgo, J., Soininen, R., Schoor, M., Korn, R., Gossler, A. (1994). Gene trap integrations in genes active in mouse embryonic stem cells efficiently detect developmentally regulated gene expression. Transgene 1, 281–291.

    CAS  Google Scholar 

  • Skarnes, W.C., Auerbach, B.A., Joyner, A.L. (1992). A gene trap approach in mouse embryonic stem-cells: the lacZ reporter is activated by splicing, reflects endogenous gene-expression, and is mutagenic in mice. Genes Dev. 6, 903–918.

    Article  PubMed  CAS  Google Scholar 

  • Solter, D. (1988). Differential imprinting and expression of maternal and paternal genomes. Annu. Rev. Genet. 22, 127–146.

    Article  PubMed  CAS  Google Scholar 

  • Surani, M.A. (1993). Genomic imprinting—silence of the genes. Nature 366, 302–303.

    Article  PubMed  CAS  Google Scholar 

  • Surani, M.A., Barton, S.C., Norris, M.L. (1984). Development of reconstituted mouse eggs suggests imprinting of the genome during gamato-genesis. Nature 308, 548–550.

    Article  PubMed  CAS  Google Scholar 

  • Surani, M.A., Reik, W., Norris, M., Barton, S. (1986). Influence of germ-line modifications of homologous chromosomes on mouse development. J. Embryol Exp. Morph 97, 123–136.

    PubMed  Google Scholar 

  • Surani, M.A., Kothary, R., Allen, N.D., Singh, P.B., Fundele, R., Ferguson-Smith, A.C., Barton, S.C. (1990). Genome imprinting and development in the mouse. Development Suppl., 89–98.

  • Surani, M.A., Sasaki, H., Ferguson-Smith, A.C., Allen, N.D., Barton, S.C., Jones, P.A., Reik, W. (1993). The inheritance of germline-specific epi-genetic modifications during development. Philos. Trans. R. Soc. Lond. 339, 165–172.

    Article  CAS  Google Scholar 

  • Swain, J.L., Stewart, T.A., Leder, P. (1987). Parental legacy determines methylation and expression of an autosomal transgene: a molecular mechanism for parental imprinting. Cell 50, 719–727.

    Article  PubMed  CAS  Google Scholar 

  • Temple, I.K., Cockwell, A., Hassold, T., Pettay, D., Jacobs, P. (1991). Maternal uniparental disomy for chromosome 14. J. Med. Genet. 28, 511–514.

    Article  PubMed  CAS  Google Scholar 

  • Wang, J.-C.C., Passage, M.B., Yen, P.H., Shapiro, L.J., Mohandas, T.K. (1991). Uniparental heterodisomy for chromosome 14 in a phenotypically abnormal familial balanced 13/14 robertsonian translocation carrier. Am. J. Hum. Genet. 48, 1069–1074.

    PubMed  CAS  Google Scholar 

  • Watanabe, T., Tarttelin, E., Neubüser, A., Kimura, M., Solter, D. (1994). Fine genetic mapping defines the genetic order of pax9, txf3a, and acrodysplasia (adp). Mamm. Genome 5, 768–770.

    Article  PubMed  CAS  Google Scholar 

  • Zachgo, J., Gossler, A. (1994). Gene trapping strategies: screens for developmentally regulated genes and insertional mutagenesis. In Towards a Molecular Analysis of Mammalian Development, P. Lonai, ed. (Amsterdam, Harwood Academic Publishers) in press.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Schuster-Gossler, K., Simon-Chazottes, D., Guénet, J.L. et al. Gtl2 lacZ, an insertional mutation on mouse Chromosome 12 with parental origin-dependent phenotype. Mammalian Genome 7, 20–24 (1996). https://doi.org/10.1007/s003359900006

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s003359900006

Keywords

Navigation