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Journal of Dental Research
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Gene Defect in Hypodontia: Exclusion of EGF, EGFR, and FGF-3 as Candidate Genes

S. Arte

Department of Pedodontics and Orthodontics, Institute of Dentistry, PO Box 41, FIN-00014 University of Helsinki, Finland

P. Nieminen

Department of Pedodontics and Orthodontics, Institute of Dentistry, PO Box 41, FIN-00014 University of Helsinki, Finland

S. Pirinen

Department of Pedodontics and Orthodontics, Institute of Dentistry, PO Box 41, FIN-00014 University of Helsinki, Finland

I. Thesleff

Department of Pedodontics and Orthodontics, Institute of Dentistry, PO Box 41, FIN-00014 University of Helsinki, Finland

L. Peltonen

Department of Human Molecular Genetics, National Public Health Institute, Finland

Hypodontia, congenital absence of one or a few permanent teeth without any systemic disorders, is regarded as an autosomally inherited dominant condition with varying expression and incomplete penetrance. Many studies have reported that the prevalence of hypodontia varies from 5% to 10% among European and Asian populations. The teeth most often missing are second premolars, upper lateral incisors, and lower central incisors. Consequently, we call this trait incisor-premolar hypodontia. Peg-shaped or strongly mesio-distally reduced upper lateral incisors demonstrate variation in the expression of the trait. The gene or genes causing incisor-premolar hypodontia are not known. We have begun the genetic mapping of hypodontia by using linkage analyses in seven Finnish three-generation families with 77 individuals, 31 affected with incisor-premolar hypodontia. As the first step, we studied the possibility of linkage between hypodontia and some candidate genes which have been suggested to have important functions during tooth development. Here we report the exclusion of EGF, EGFR, and FGF-3 loci as possible sites for gene mutation causing incisor-premolar hypodontia in our family material. Because of the close location of the FGF-3 and FGF-4 genes, the results also suggest the exclusion of the FGF-4 locus.

Key Words: hypodontia • linkage analysis • growth factors • growth factor receptors • tooth development

REFERENCES

  • Aasheim B., Ogaard B. (1993). Hypodontia in 9-year-old Norwegians related to need of orthodontic treatment. Scand J Dent Res 101:257-260.[Medline] [Order article via Infotrieve]
  • Alvesalo L., Portin P. (1969). The inheritance pattern of missing, peg-shaped and strongly mesio-distally reduced upper lateral incisors. Acta Odontol Scand 27:563-573.[Medline] [Order article via Infotrieve]
  • Bjerklin K., Kurol J., Valentin J. (1992). Ectopic eruption of maxillary first permanent molars and association with other tooth and developmental disturbances. Eur J Orthod 14:369-375.[Abstract/Free Full Text]
  • Brookes S., Lammie GA, Schuuring E., Dickson C., Peters G. (1992). Linkage map of region of human chromosome band llql3 amplified in breast and squamous cell tumors. Genes Chromos Cancer 4:290-301.
  • Burzynski N., Escobar V. (1983). Classification and genetics of numeric anomalies of dentition. Birth Defects: Orig Art Ser 13:95-106.
  • Chi DD, Hing AV, Helms C., Steinbrueck T., Mishra SK, Donis-Keller H. (1992). Two chromosome 7 dinucleotide repeat polymorphisms at gene loci epidermal growth factor receptor (EGFR) and proa2(I)collagen (COL1A2). Hum Molec Genet 1:135.[Free Full Text]
  • Cohen MM Jr (1995). Craniosynostoses: Phenotypic/molecular correlations. Am J Med Genet 56:334-339.[CrossRef][Medline] [Order article via Infotrieve]
  • Cohn MJ, Izpisua-Belmonte JC, Abud H., Heath JK, Tickle C. (1995). Fibroblast growth factors induce additional limb development from the flank of chick embryos. Cell 80:739-746.[CrossRef][Medline] [Order article via Infotrieve]
  • Davis PJ (1987). Hypodontia and hyperdontia of permanent teeth in Hong Kong schoolchildren. Community Dent Oral Epidemiol 15:218-220.[CrossRef][Medline] [Order article via Infotrieve]
  • Gorlin RJ, Cohen MM Jr, Levin SL, editors (1990). Syndromes of the head and neck. 3rd ed. New York: Oxford University Press.
  • Grahnen H. (1956). Hypodontia in the permanent dentition. Odont Revy 7(Suppl 3):1-100.
  • Haavikko K. (1971). Hypodontia of permanent teeth. An orthopantomographic study. Suom Hammaslääk Toim 67:219-225.[Medline] [Order article via Infotrieve]
  • Jernvall J., Kettunen P., Karavanova I., Martin LB, Thesleff I. (1994). Evidence for the role of the enamel knot as a control center in mammalian tooth cusp formation: non-dividing cells express growth stimulating Fgf-4 gene. Int J Dev Biol 38:463-469.[Medline] [Order article via Infotrieve]
  • Keiser-Nielsen S. (1971). Federation Dentaire Internationale two-digit system of designating teeth. Int Dent J 21:104-106.
  • Kere J., Grzeschik K-H., Limon J., Gremaud M., Schlessinger D., de la Chapelle A. (1993). Anhidrotic ectodermal dysplasia gene region cloned in yeast artificial chromosomes. Genomics 16:305-310.[Medline] [Order article via Infotrieve]
  • Kronmiller JE, Upholt WB, Kollar EJ (1991). EGF antisense oligonucleotides block murine odontogenesis in vitro. Dev Biol 147:485-488.[CrossRef][Medline] [Order article via Infotrieve]
  • Lathrop GM, Laouel JM, Julier J., Ott J. (1984). Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci USA 81:3443-3446.[Abstract/Free Full Text]
  • Lumsden AGS (1988). Spatial organization of the epithelium and the role of neural crest cells in the initiation of mammalian tooth germ. Development 103:155-169.[Abstract/Free Full Text]
  • MacKenzie A., Leeming GL, Jowett AK, Ferguson MJW, Sharpe PT (1991). The homeobox gene Hox 7.1 has specific regional and temporal expression patterns during early murine craniofacial embryogenesis, especially tooth development in vivo and in vitro. Development 111:269-285.[Abstract]
  • MacKenzie A., Ferguson MWJ, Sharpe PT (1992). Expression patterns of the homeobox gene, Hox 8, in the mouse embryo suggest a role in specifying tooth initiation and shape. Development 115:403-420.[Abstract]
  • Magnusson TE (1977). Prevalence of hypodontia and malformations of permanent teeth in Iceland. Community Dent Oral Epidemiol 5:173-178.[CrossRef][Medline] [Order article via Infotrieve]
  • Mansour SL, Goddard JM, Capecchi MR (1993). Mice homozygous for a targeted disruption of the proto-oncogene Int-2 have developmental defects in the tail and inner ear. Development 117:13-28.[Abstract/Free Full Text]
  • Mina M., Kollar EJ (1987). The induction of odontogenesis in non-dental mesenchyme combined with early murine mandibular arch epithelium. Arch Oral Biol 32:123-127.[CrossRef][Medline] [Order article via Infotrieve]
  • Murray JC, Bennett SR, Kwitek AE, Small KW, Schinzel A., Alward WIM et al. (1992). Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4. Nature Genet 2:46-49.[CrossRef][Medline] [Order article via Infotrieve]
  • Nieminen P., Arte S., Pirinen S., Peltonen L., Thesleff I. (1995). Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes. Hum Genet 96:305-308.[Medline] [Order article via Infotrieve]
  • Niswander L., Martin GR (1992). Fgf-4 expression during gastrulation, myogenesis, limb and tooth development in the mouse. Development 114:755-768.[Abstract]
  • Ott J. (1974). Estimation of recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. Am J Hum Genet 26:588-597.[Medline] [Order article via Infotrieve]
  • Ott J. (1989). Computer-simulation methods in human linkage analysis. Proc Natl Acad Sci USA 86:4175-4178.[Abstract/Free Full Text]
  • Partanen A-M., Ekblom P., Thesleff I. (1985). Epidermal growth factor inhibits morphogenesis and cell differentation in cultured mouse embryonic teeth. Dev Biol 111:84-94.[CrossRef][Medline] [Order article via Infotrieve]
  • Peck L., Peck S., Attia Y. (1993). Maxillary canine-first premolar transposition, associated dental anomalies and genetic bases. Angle Orthod 63:99-109.[Medline] [Order article via Infotrieve]
  • Peck S., Peck L., Kataja M. (1994). The palatally displaced canine as a dental anomaly of genetic origin. Angle Orthod 64:249-256.[Medline] [Order article via Infotrieve]
  • Peters K., Werner S., Liao X., Wert S., Whitsett J., Williams L. (1994). Targeted expression of a dominant negative FGF receptor blocks branching morphogenesis and epithelial differentiation of the mouse lung. EMBO J 13: 3296-3301.[Medline] [Order article via Infotrieve]
  • Polymeropoulos MH, Xiao H., Rath DS, Merril CR (1990). Dinucleotide repeat polymorphism at the int-2 proto-oncogene locus (INT2). Nucleic Acids Res 18:7468.[Free Full Text]
  • Rolling S. (1980). Hypodontia of permanent teeth in Danish schoolchildren. Scand J Dent Res 88:365-369.[Medline] [Order article via Infotrieve]
  • Sambrook J., Fritsch EF, Maniatis T. (1989). Molecular cloning. A laboratory manual. 2nd ed. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press.
  • Satokata I., Maas R. ( 1994). Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nature Genet 6:348-355.[CrossRef][Medline] [Order article via Infotrieve]
  • Schalk-van der Weide Y. (1992). Oligodontia. A clinical, radiographic and genetic evaluation (thesis). Utrecht, The Netherlands: University of Utrecht.
  • Suarez CK, Spence A. (1974). The genetics of hypodontia. J Dent Res 53:781-785.
  • Svinhufvud E., Myllarniemi S., Norio R. (1988). Dominant inheritance of tooth malpositions and their association to hypodontia. Clin Genet 34:373-381.[Medline] [Order article via Infotrieve]
  • Thesleff I., Vaahtokari A. (1992). The role of growth factors in determination and differentiation of the odontoblastic cell lineage. Proc Finn Dent Soc 88(Suppl I):357-368.[Medline] [Order article via Infotrieve]
  • Thesleff I., Vaahtokari A., Vainio S. (1990). Molecular changes during determination and differentiation of the dental mesenchymal cell lineage. J Biol Buccale 18:179-188.[Medline] [Order article via Infotrieve]
  • Vainio S., Thesleff I. (1992). Coordinated induction of cell proliferation and syndecan expression in dental mesenchyme by epithelium: evidence for diffusible signals. Dev Dynam 194:105-117.[Medline] [Order article via Infotrieve]
  • Vainio S., Karavanova I., Jowett A., Thesleff I. (1993). Identification of BMP-4 as a signal mediating secondary induction between epithelial and mesenchymal tissues during early tooth development. Cell 75:45-58.[CrossRef][Medline] [Order article via Infotrieve]
  • Vandenplas S., Wiid I., Grobler-Rabie A., Brebner K., Ricketts M., Wallis G., et al. (1984). Blot hybridisation analysis of genomic DNA. J Med Genet 21:164-172.[Abstract/Free Full Text]
  • Weeks DE, Ott J., Lathrop GM (1990). SLINK: a general simulation program for linkage analysis (abstract). Am J Hum Genet 47:A204.
  • Weissenbach J., Gyapay G., Dip C., Vignal A., Morissette J., Millasseau P., et al. (1992). A second-generation linkage map of the human genome. Nature 359:794-801.[CrossRef][Medline] [Order article via Infotrieve]
  • Wilkinson GD, Bhatt S., McMahon AP (1989). Expression pattern of the FGF-related proto-oncogene int-2 suggests multiple roles in fetal development. Development 105:131-136.[Abstract]
  • Yamaguchi TP, Rossant J. (1995). Fibroblast growth factors in mammalian development (review). Curr Opin Genet & Dev 5:485-491.[CrossRef][Medline] [Order article via Infotrieve]

Journal of Dental Research, Vol. 75, No. 6, 1346-1352 (1996)
DOI: 10.1177/00220345960750060401


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