Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt) (original) (raw)
References
Fahrner, K., Hogan, B.L.M., and Flavell, R.A.: Transcription of H-2 and Qa genes in embryonic and adult mice. EMBO J 6: 1265–1271, 1987. Google Scholar
Franz, T. and Beseke, A.: The development of the eye in homozygous mutants of the extra-toes locus of the mouse. Anat Embryol 184: 335–361, 1991. Google Scholar
Gollop, T.R. and Fontes, L.R.: The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature. Am J Med Genet 22: 59–68, 1985. Google Scholar
Johnson, D.R.: Extra-toes: a new mutant gene causing multiple abnormalities in the mouse. J Embryol Exp Morphol 17: 543–581, 1967. Google Scholar
Krüger, G., Götz, J., Kvist, U., Dunker, H., Erfurth, F., Pelz, L. and Zech, L.: Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13). Am J Med Genet 32: 411–416, 1989. Google Scholar
Kunkel, L.M., Tantravahi, U., Eisenhard, M., and Latt, S.A.: Regional localization on the human X of DNA segments cloned from flow sorted chromosomes. Nucleic Acids Res 10: 1557–1578, 1982. Google Scholar
Pettigrew, A.L., Greenberg, F., Caskey, C.T., and Ledbetter, D.H.: Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13. Hum Genet87:452–456, 1991. Google Scholar
Pohl, T.M., Mattei, M.G., and Rüther, U.: Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra-toes (Xt). Development 110: 1153–1157, 1990. Google Scholar
Ruppert, J.M., Kinzler, K.W., Wong, A.J., Bigner, S.H., Kao, F.-T., Law, M.I., Seuanez, H.N., O'Brien, S.J., and Vogelstein, B.: The GLI-Krüppel family of human genes. Mol Cell Biol 8: 3104–3113, 1988. Google Scholar
Ruppert, J.M., Vogelstein, B., Arheden, K., and Kinzler, K.W.: GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity. Mol Cell Biol 10: 5408–5415, 1990. Google Scholar
Sambrook, J., Fritsch, E.G., and Maniatis, T.: Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989. Google Scholar
Tommerup, N. and Nielsen, F.: A familial reciprocal translocation (3;7)(p21.1;p13) associated with the Greig polysyndactylycraniofacial anomalies syndrome. Am J Med Genet 22: 313–321, 1983. Google Scholar
Vortkamp, A., Gessler, M., and Grzeschik, K.-H.: GLI3 zinc finger gene interrupted by translocations in Greig syndrome families. Nature 352: 539–540, 1991a. Google Scholar
Vortkamp, A., Thias, U., Gessler, M., Rosenkranz, W., Kroisel, P.M., Tommerup, N., Krüger, G., Götz, J., Pelz, L., and Grzeschik, K.-H.: A somatic cell hybrid panel and DNA probes for physical mapping of human chromosome 7p. Genomics 11: 737–743, 1991b. Google Scholar
Wagner, K., Kroisel, P.M., and Rosenkranz, W.: Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes. Genomics 8: 487–491, 1990. Google Scholar
Winter, R.M. and Huson, S.M.: Greig cephalopolysyndactyly syndrome: a possible mouse homologue (_Xt_-extra toes). Am J Med Genet 31: 793–798, 1988. Google Scholar