The genetic basis of normal and abnormal craniofacial development

Acta Odontologica Scandinavica

Volumn 56, Issue 6, 1998, Pages 321-325

  Thesleff, Irma ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

Author keywords

Bone development; Craniofacial defects; Hypodontia; Signaling network; Tooth development

Indexed keywords

TRANSCRIPTION FACTOR;

ANIMAL; BONE DEVELOPMENT; CELL COMMUNICATION; CRANIOFACIAL MALFORMATION; FACE; FACIAL BONE; GENETIC TRANSCRIPTION; GENETICS; HUMAN; JAW; MAXILLOFACIAL DEVELOPMENT; MORPHOGENESIS; MOUSE; MUTATION; PRENATAL DEVELOPMENT; REVIEW; SIGNAL TRANSDUCTION; SKULL; TOOTH DEVELOPMENT;

ANIMALS; BONE DEVELOPMENT; CELL COMMUNICATION; CRANIOFACIAL ABNORMALITIES; FACE; FACIAL BONES; HUMANS; JAW; MAXILLOFACIAL DEVELOPMENT; MICE; MORPHOGENESIS; MUTATION; ODONTOGENESIS; SIGNAL TRANSDUCTION; SKULL; TRANSCRIPTION FACTORS; TRANSCRIPTION, GENETIC;

EID: 0032242218     PISSN: 00016357     EISSN: None     Source Type: Journal    
DOI: 10.1080/000163598428248     Document Type: Article

References (39)

1. Gilbert SF. Developmental biology. 5th ed. Sunderland (MA): Sinauer Associates; 1997.
2. Satokata I, Maas R. Msxl deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nat Genet 1994;6:348-56.
3. Yamada G, Mansouri A, Torres M, Stuart ET, Blum M, Schultz M, et al. Targeted mutation of the murine goosecoid gene results in craniofacial defects and neonatal death. Development 1995;121: 2917-22.
4. Qiu M, Bulfone A, Martinez S, Meneses JJ, Shimamura K, Pedersen RA, et al. Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain. Genes Dev 1995;9:2523-38.
5. Martin J, Bradley A, Olson E. The paired-like homeo box gene Mhox is required for early events of skeletogenesis in multiple lineages. Genes Dev 1995;9:1237-19.
6. Callaerts P, Halder G, Gehring WJ. PAX-6 in development and evolution. Ann Rev Neurosci 1997;20:483-532.
7. Shawlot W, Behringer RR. Requirement for Lim1 in head-organizer function. Nature 1995;374:425-30.
8. Van Genderen C, Okamura RM, Farinas I, Quo RG, Parslow TG, Bruhn L, et al. Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1 deficient mice. Genes Dev 1994;8:2691-703.
9. Qiu M, Bulfone A, Ghattas I, Meneses J, Sharpe PT, Presley R, et al. Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from first and second arches. Dev Biol 1997;185:165-84.
10. Peters H, Neubuser A, Balling R. Pax genes and organogenesis: Pax9 meets tooth development. Eur J Oral Sci 1998;106:38-43.
11. Bei M, Maas R. FGFs and BMP4 induce both Msx1-independent and Msx1-dependent signaling pathways in early tooth development. Development 1998;125:4325-33.
12. D'Souza RN, Åberg T, Gaikwad J, Cavender A, Owen M, Karsenty G, et al. Osf2 is required for epithelial-mesenchymal interactions regulating tooth morphogenesis in mice. In press 1999.
13. Ducy P, Zhang R, Geoffroy V, Ridall AL, Karsenty G. Osf2/ Cbfa1: a transcriptional activator of osteoblast differentiation. Cell 1997;89:747-54.
14. Mundlos S, Otto F, Mundlos C, Mulliken JB, Aylsworth AS, Albright S, et al. Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia. Cell 1997;89:773-9.
15. Hogan BL. Bone morphogenetic proteins in development. Curr Opin Genet Dev 1996;6:432-8.
16. Thesleff I, Nieminen P. Tooth morphogenesis and cell differentiation. Curr Opin Cell Biol 1996;8:844-50.
17. Developmental Biology Programme, University of Helsinki. Gene expression in tooth [Internet database]. 1998. Available from URL: http://honeybee.helsinki.fi/toothexp
18. Cohn MJ, Izpisua-Belmonte JC, Abud H, Heath JK, Tickle C. Fibroblast growth factors induce additional limb development from the flank of chick embryos. Cell 1995;80:739-46.
19. Tickle C. Vertebrate limb development. Curr Opin Genet Dev 1995;5:478-84.
20. Wozney J. The bone morphogenetic protein family and osteogenesis. Mol Reprod Dev 1992;32:160-7.
21. Kronenberg HM, Lee K, Lanske B, Segre GV. Parathyroid hormone-related protein and Indian hedgehog control the pace of cartilage differentiation. J Endocrinol 1997;154 Suppl:S39-45.
22. Clouthier DE, Hosoda K, Richardson JA, Williams SC, Yanagisawa H, Kuwaki T, et al. Cranial and cardiac neural crest defects in endothelin-A receptor-deficient mice. Development 1998;125:813-24.
23. Roessler E, Belloni E, Gandenz K, Jay P, Berta P, Scherer SW, et al. Mutations in the human Sonic Hedgehog gene cause holoprosencephaly. Nat Genet 1996;14:357-60.
24. Wilkie AOM, Slaney SF, Oldridge M, Poole MD, Ashworth GJ, Hockley AD, et al. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nat Genet 1995;9:165-72.
25. Muenke M, Schell U, Hehr A, Robin NH, Losken HW, Schinzel A, et al. A common mutation in the fibroblast growth factor receptor 1 in gene Pfeiffer syndrome. Nat Genet 1994;8:269-74.
26. Jabs EW, Li X, Scott AF, Meyers G, Chen W, Eckles M, et al. Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2. Nat Genet 1994;8:275-9.
27. Howard TD, Paznekas WA, Green ED, Chiang LC, Ma N, Ortiz de Luna RI, et al. Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome. Nat Genet 1997;15:36-11.
28. el Ghouzzi V, Le Merrer M, Perrin-Schmitt F, Lajeunie E, Benit P, Renier D, et al. Mutations of the TWIST gene in the Saethre-Chotzen syndrome. Nat Genet 1997;15:42-6.
29. Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE. A human MSX1 homeodomain missense mutation causes selective tooth agenesis. Nat Genet 1996;13:417-21.
30. Semina EV, Reiter R, Leysens NJ, Alward WL, Small KW, Datson NA, et al. Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nat Genet 1996;14:392-9.
31. Kere J, Srivastava AK, Montonen O, Zonana J, Thomas N, Ferguson B, et al. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nat Genet 1996;13:379-80.
32. Spranger J, Winterpacht A, Zabel B. The type II collagenopathies: a spectrum of chondrodysplasias. Eur J Pediatr 1994; 153:56-65.
33. Forsman S, Lind L, Bäckman B, Westermark E, Holmgren G. Localization of a gene for autosomal dominant amelogenesis imperfecta (ADAI) to chromosome 4q. Hum Mol Genet 1994; 3:1621-5.
34. Otto F, Thornell AP, Crompton T, Denzel A, Gilmour KC, Rosewell IR, et al. Cbfa 1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development. Cell 1997;89:765-71.
35. Srivastava A, Pispa J, Hartung P, Du Y, Ezer S, Jenks T, et al. Tabby phenotype is caused by mutation in mouse homologue of EDA gene, which reveals novel human exons and encodes a protein (ectodysplasin-A) with collagenous domains. Proc Natl Acad Sci U S A 1997;94:13069-74.
36. Huang L-F, Fukai N, Selby PB, Olsen BR, Mundlos S. Mouse clavicular development: analysis of wild-type and cleidocranial dysplasia mutant mice. Dev Dyn 1997;210:33-40.
37. Chen Y, Bei M, Woo I, Satokata I, Maas R. Msx1 controls inductive signaling in mammalian tooth morphogenesis. Development 1996;122:3035-44.
38. Kim H-J, Rice DPC, Kettunen PJ, Thesleff I. FGF, BMP, and Shh mediated signalling pathways in the regulation of cranial suture morphogenesis and calvarial bone development. Development 1998;125:1241-51.
39. Blecher SR, Kapalanga J, Lalonde D. Induction of sweat glands by epidermal growth factor in murine X-linkcd anhidrotic ectodermal dysplasia. Nature 1990;345:542-4.