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Brown, C.F., Lafreuiere, R.G., Powers, V.E., Sebastio, G., Ballabio, A., Pettigrew, A.L., Ledbetter, D.H., Levy, E., Craig, I.W., and Willard, H.F.: Localization of the X inactivation centre on the human X chromosome in Xq13. Nature 349: 82–84, 1991.
Eissenberg, J.C.: Position effect variegation in Drosophila: towards a genetics of chromatin assembly. Bioessays 11: 14–17, 1989.
Eissenberg, J.C., James, T.C., Foster-Hartnett, D.M., Hartnett, T., Ngan, V., and Elgin, S.C.R.: Mutation in a heterochromatin-specific chromosomal protein is associated with suppressor of position-effect variegation in Drosophila melanogaster. Proc Natl Acad Sci USA 87: 9923–9927, 1990.
Fan, Y.-S., Davis, L.M., and Shows, T.B.: Mapping small DNA sequences by fluorescence in situ hybridization onto banded chromosomes. Proc Natl Acad Sci USA 87: 6223–6227, 1990.
Gaunt, S.J. and Singh, P.B.: Homeogene expression patterns and chromosomal imprinting. Trends Genet 6: 208–212, 1990.
Hamvas, R.M.J., Reik, W., Gaunt, S.J., Brown, S.D.M., and Singh, P.B.: Mapping of a mouse homolog of a Heterochromatin protein gene to the X Chromosome. Mammalian Genome 2: 72–75, 1992.
James, T.C. and Elgin, S.C.R.: Identification of a non-histone chromosomal protein associated with heterochromatin in Drosophila melanogaster and its gene. Mol Cell Biol 6: 3862–3872, 1986.
Kievits, T., Dauwerse, J.G., Wiegant, J., Devilee, P., Breuning, M.H., Cornelisse, C.J., van Ommen G.-J.B., and Pearson, P.L.: Rapid subchromosomal localization of cosmids by non-radioactive in situ hybridization. Cytogenet Cell Genet 53: 134–136, 1990.
Laird, C.D.: Proposed genetic basis of Huntington's disease. Trends Genet 6: 242–247, 1990.
Lyon, M.F.: The quest for the X-inactivation center. Trends Genet 7: 69–70, 1991.
Paro, R.: Imprinting a determined state into the chromatin of Drosophila melanogaster. Trends Genet 6: 416–421, 1990.
Paro, R. and Hogness, D.S.: The polycomb protein shares a homologous domain with a heterochromatin-associated protein of Drosophila. Proc Natl Acad Sci USA 88: 263–267, 1991.
Sapienza, C.: Sex-linked dosage-sensitive modifiers as imprinting genes. Development (Suppl): 107–114, 1990.
Singh, P.B., Miller, J.R., Pearce, J., Kothary, R., Burton, R.D., Paro, R., James, T.C., and Gaunt, S.J.: A sequence motif found in a Drosophila heterochromatin protein is conserved in animals and plants. Nucleic Acids Res 19: 789–794, 1991.
Spofford, J.: Position effect variegation in Drosophila. In M. Ashburner and E. Novitski (eds.); The Genetics and Biology of Drosophila, pp. 955–1018, Academic Press, New York, 1976.
Viegas-Pequignot, E., Dutrillaux, B., Magdelenat, H., and Coppey-Moisan, M.: Mapping of single-copy DNA sequences on human chromosomes by in situ hybridization with biotinylated probes: enhancement of detection sensitivity by intensified-fluorescence digital-imaging microscopy. Proc Natl Acad Sci USA 86: 582–586, 1989.
Weiner, A.M., Deininger, P.L., and Efstratiadis, A.: Nonviral retroposons: genes, pseudogenes and transposable elements generated by the reverse flow of genetic information. Annu Rev Biochem 55: 631–661, 1986.
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Reik, W., Leversha, M.A., Waterfield, N.R. et al. Mapping of two human homologs of a Drosophila heterochromatin protein gene to the X Chromosome. Mammalian Genome 3, 650–652 (1992). https://doi.org/10.1007/BF00352483
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DOI: https://doi.org/10.1007/BF00352483