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Genomic mapping within the albino-deletion complex using individual early postimplantation mouse embryos

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Abstract

Sensitive methods for analysis of DNA from limited amounts of tissue are often difficult, error prone, and time consuming. Here, we describe a procedure for molecular analysis of individual early post-implantation mouse embryos by Southern analysis. The procedure involves embedding single embryos in agarose before lysing and deproteinizing in situ. The embedded DNA can be digested with restriction enzymes and analyzed by standard Southern-blotting procedures. The procedure is sensitive enough to detect single-copy sequences in embryos as early as day 6.5 of development. We have used the technique to genotype embryos homozygous for an embryonic lethal deletion. Normally, the lethal phenotype associated with such mutations is identified by a retrospective statistical analysis of abnormal embryos produced from a heterozygous cross as compared to those produced from a control cross. Now, if associated with a detectable DNA abnormality, the mutant embryo can be genotyped directly. We also report the use of this method for mapping cloned markers relative to deletion breakpoints. This approach can save considerable time since mapping would conventionally be done using restriction fragment length polymorphisms (RFLPs) detected in Mus musculus/Mus spretus interspecies hybrids. Using this procedure, we have been able to redefine the distal limits of the region of Chromosome (Chr) 7 containing a gene (eed) needed for development of the embryonic ectoderm.

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References

  • Boultwood, J., Abrahamson, G.M. and Wainscoat, J.S.: Structural DNA analysis from a single hair root by standard or pulsed field gel electrophoresis. Nucl Acids Res 18: 4628, 1990.

    Google Scholar 

  • Church, G.M. and Gilbert, W.: Genomic Sequencing. Proc Natl Acad Sci USA 81: 1991–1995, 1984.

    Google Scholar 

  • D'Eustachio, P., Owens, G.C., Edelman, G.M. and Cunningham, B.A.: Chromosomal location of the gene encoding the neural cell adhesion molecule (N-CAM) in the mouse. Proc Natl Acad Sci USA 82: 7631–7635, 1985.

    Google Scholar 

  • Disteche, C.M., and Alder, D.: Localization of cloned mouse chromosome 7-specific DNA to lethal albino deletions. Som Cell Mol Genet 10: 211–215, 1984.

    Google Scholar 

  • Eicher, E.M., Lewis, S.E., Turchin, H.A. and Gluecksohn-Waelsch, S.: Absence of mitochondrial malic enzyme in mice carrying two complementing lethal albino alleles. Genet Res Camb 32: 1–7, 1978.

    Google Scholar 

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

    Google Scholar 

  • Gluecksohn-Waelsch, S.: Regulatory genes in development. Trend Genet 3: 123–127, 1987.

    Google Scholar 

  • Gluecksohn-Waelsch, S., Schiffman, M.B., Thorndike, J. and Cori, C.F.: Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase and serine dehydratase. Proc Natl Acad Sci USA 71: 825–829, 1974.

    Google Scholar 

  • Higuchi, R., von Beroldingen, C.H., Sensabaugh, G.F., and Erlich, H.A.: DNA typing from single hairs. Nature 332: 543–546, 1988.

    Google Scholar 

  • Johnson, D.K., Hand, R.E., and Rinchik, E.M.: Molecular mapping within the mouse albino-deletion complex. Proc Natl Acad Sci USA 86: 8862–8866, 1989.

    Google Scholar 

  • Klebig, M.L., Kwon, B.S., and Rinchik, E.M.: Physical analysis of murine albino deletions that disrupt liver-specific gene regulation or mesoderm development. Mammalian Genome 2: 51–63, 1992.

    Google Scholar 

  • Kwok, S. and Higuchi, R.: Avoiding false positives with PCR. Nature 339: 237–238, 1989.

    Google Scholar 

  • Lewis, S.E., Turchin H.A., and Gluecksohn-Waelsch, S.: The developmental analysis of an embryological lethal (c 6H) in the mouse. J Embryol Exp Morph 36: 363–371, 1976.

    Google Scholar 

  • McKnight, S.L., Lane, M.D., and Gluecksohn-Waelsch, S.: Is CCAAT/enhancer-binding protein a central regulator of energy metabolism? Genes Develop 3: 2021–2024, 1989.

    Google Scholar 

  • Maniatis, T., Fritsch, E.F., and Sambrook, J.: Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, New York, 1982.

    Google Scholar 

  • Nadijcka, M.D., Hillman, N., and Gluecksohn-Waelsch, S.: Ultrastructural studies of lethal c 25H /c 25H mouse embryos. J Embryol Exp Morph 52: 1–11, 1979.

    Google Scholar 

  • Nguyen, C., Mattei, M.-G., Mattei, J.-F., Santoni, M.-J., Goridis, C., and Jordan, B.R.: Localization of the human NCAM gene to band q23 of chromosome 11: The third gene coding for a cell interaction molecular mapped to the distal portion of the long arm of chromosome 11. J Cell Biol 102: 711–715, 1986.

    Google Scholar 

  • Niswander, L., Yee, D., Rinchik, E.M., Russell, L.B. and Magnuson, T.: The albino deletion complex and early postimplantation survival in the mouse. Development 102: 45–53, 1988.

    Google Scholar 

  • Niswander, L., Yee, D., Rinchik, E.M., Russell, L.B., and Magnuson, T.: The albino deletion complex in the mouse defines genes necessary for development of embryonic and extraembryonic ectoderm. Development 105: 175–182, 1989.

    Google Scholar 

  • Niswander, L., Kelsey, G., Schedl, A., Ruppert, S., Sharan, S.K., Holdener-Kenny, B., Rinchik, E.M., Edström, J.-E., and Magnuson, T.: Molecular mapping of albino deletions associated with early embryonic lethality in the mouse. Genomics 9: 162–169, 1991.

    Google Scholar 

  • Rappolee, D.A., Brenner, C.A., Schultz, R., Mark, D. and Werb, Z.: Developmental expression of PDGF, TGF-α, and TGF-β genes in preimplantation mouse embryos. Science 241: 1823–1825, 1988.

    Google Scholar 

  • Russell, L.B., Montgomery, C.S., Raymer, G.D.: Analysis of the albino-locus of the mouse. IV. Characterization of 34 deficiencies. Genetics 100: 427–453, 1982.

    Google Scholar 

  • Saunders, A.M. and Seldin, M.F.: A molecular genetic linkage map of mouse chromosome 7. Genomics 8: 525–535, 1990.

    Google Scholar 

  • Sharan, S.K., Holdener-Kenny, B., Ruppert, S., Schedl, G., Rinchik, E.M., and Magnuson, T.: The albino deletion complex of the mouse: Molecular mapping of deletion breakpoints that define regions necessary for development of the embryonic and extraembryonic ectoderm. Genetics 129:825–832, 1991.

    Google Scholar 

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Sharan, S.K., Holdener-Kenny, B., Threadgill, D.W. et al. Genomic mapping within the albino-deletion complex using individual early postimplantation mouse embryos. Mammalian Genome 3, 79–83 (1992). https://doi.org/10.1007/BF00431250

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