TFII-I gene family during tooth development: Candidate genes for tooth anomalies in Williams syndrome

Developmental Dynamics

Volumn 236, Issue 10, 2007, Pages 2884-2888

  Ohazama, Atsushi ^a,b   Sharpe, Paul T ^a,c  

^a KING'S COLLEGE LONDON   (United Kingdom)

^b SHOWA UNIVERSITY SCHOOL OF DENTISTRY   (Japan)

^c GUY S HOSPITAL   (United Kingdom)

Author keywords

Candidate genes; Epithelium; Gtf2i; Gtf2ird1; Gtf2ird2; In situ hybridization; Incisor; Mesenchyme; Molar; TFII I gene family; Tooth development; Williams syndrome

Indexed keywords

CELL PROTEIN; COMPLEMENTARY DNA; PROTEIN GTF2I; PROTEIN GTF2IRD1; PROTEIN GTF2IRD2; UNCLASSIFIED DRUG;

AMELOBLAST; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CARDIOVASCULAR DISEASE; CHROMOSOME 7Q; CONTROLLED STUDY; FACE MALFORMATION; GENE; GENE DELETION; HETEROZYGOSITY; IN SITU HYBRIDIZATION; MENTAL DEFICIENCY; MOUSE; MULTIGENE FAMILY; NONHUMAN; ODONTOBLAST; PRIORITY JOURNAL; PROTEIN EXPRESSION; TELOMERE; TFII I GENE; TOOTH DEVELOPMENT; TOOTH MALFORMATION; WILLIAMS BEUREN SYNDROME;

ANIMALS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 7; HUMANS; MICE; MUSCLE PROTEINS; NUCLEAR PROTEINS; ODONTOGENESIS; TOOTH; TRANS-ACTIVATORS; TRANSCRIPTION FACTORS, TFII; WILLIAMS SYNDROME;

MURINAE;

EID: 35349017356     PISSN: 10588388     EISSN: 10970177     Source Type: Journal    
DOI: 10.1002/dvdy.21311     Document Type: Article

References (18)

1. Angerer LM, Angerer RC. 1992. In situ hybridisation to cellular RNA with radiolabelled RNA probes. In: Wilkinson DG, editor. In situ hybridisation: a practical approach. Oxford: Oxford University Press. p 15-30.
2. Axelsson S. 2005. Variability of the cranial and dental phenotype in Williams syndrome. Swed Dent J Suppl:3-67.
3. Axelsson S, Bjornland T, Kjaer I, Heiberg A, Storhaug K. 2003. Dental characteristics in Williams syndrome: a clinical and radiographic evaluation. Acta Odontol Scand 61:129-136.
4. Bayarsaihan D, Ruddle FH. 2000. Isolation and characterization of BEN, a member of the TFII-I family of DNA-binding proteins containing distinct helix-loop-helix domains. Proc Natl Acad Sci U S A 97: 7342-7347.
5. Bayarsaihan D, Bitchevaia N, Enkhmandakh B, Tussie-Luna MI, Leckman JF, Roy A, Ruddle F. 2003. Expression of BEN, a member of TFII-I family of transcription factors, during mouse pre- and postimplantation development. Gene Expr Patterns 3:579-589.
6. Donnai D, Karmiloff-Smith A. 2000. Williams syndrome: from genotype through to the cognitive phenotype. Am J Med Genet 97:164-171.
7. Hertzberg J, Nakisbendi L, Needleman HL, Pober B. 1994. Williams syndrome-oral presentation of 45 cases. Pediatr Dent 16:262-267.
8. Kashyap AS, Sharma HS, Kumar P. 2000. Dental anomalies in Williams syndrome. Postgrad Med J 76:712.
9. Morris CA, Mervis CB. 2000. Williams Syndrome and related disorders. Annu Rev Genomics Hum Genet 1:461-484.
10. Ohazama A, Sharpe PT. 2003. Development of epidermal appendages; teeth and hair. In: Epstein CJ, Erickson RP, Wynshaw-Boris A editors. Molecular basis of inborn errors of development. Oxford, New York: Oxford University Press. p 199-209.
11. O'Mahoney JV, Guven KL, Lin J, Joya JE, Robinson CS, Wade RP, Hardeman EC. 1998. Identification of a novel slow-muscle-fiber enhancer binding protein, MusTRD1. Mol Cell Biol 18:6641-6652.
12. Palmer SJ, Tay ES, Santucci N, Cuc Bach TT, Hook J, Lemckert FA, Jamieson RV, Gunnning PW, Hardeman EC. 2007. Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development. Gene Expr Patterns 7:396-404.
13. Roy AL, Du H, Gregor PD, Novina CD, Martinez E, Roeder RG. 1997. Cloning of an inr- and E-box-binding protein, TFII-I, that interacts physically and functionally with USF1. EMBO J 16:7091-7104.
14. Tarjan I, Balaton G, Balaton P, Varbiro S, Vajo Z. 2003. Facial and dental appearance of Williams syndrome. Postgrad Med J 79:241.
15. Tassabehji M, Carette M, Wilmot C, Donnai D, Read AP, Metcalfe K. 1999. A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndrome. Eur J Hum Genet 7:737-747.
16. Tassabehji M, Hammond P, Karmiloff-Smith A, Thompson P, Thorgeirsson SS, Durkin ME, Popescu NC, Hutton T, Metcalfe K, Rucka A, Stewart H, Read AP, Maconochie M, Donnai D. 2005. GTF2IRD1 in craniofacial development of humans and mice. Science 310:1184-1187.
17. Tipney HJ, Hinsley TA, Brass A, Metcalfe K, Donnai D, Tassabehji M. 2004. Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome. Eur J Hum Genet 12:551-560.
18. Tucker AS, Al Khamis A, Sharpe PT. 1998. Interactions between Bmp-4 and Msx-1 act to restrict gene expression to odontogenic mesenchyme. Dev Dyn 212:533-539.