PUBLICATION
SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma
- Authors
- Gregory-Evans, C.Y., Moosajee, M., Hodges, M.D., Mackay, D.S., Game, L., Vargesson, N., Bloch-Zupan, A., Rüschendorf, F., Santos-Pinto, L., Wackens, G., and Gregory-Evans, K.
- ID
- ZDB-PUB-070806-17
- Date
- 2007
- Source
- Human molecular genetics 16(20): 2482-2493 (Journal)
- Registered Authors
- Keywords
- none
- MeSH Terms
-
- Animals
- Chromosome Mapping*
- Chromosomes, Human, Pair 11*
- Coloboma/genetics*
- Craniofacial Abnormalities/genetics
- DNA Mutational Analysis
- Embryo, Nonmammalian
- Eye/embryology
- Fas-Associated Death Domain Protein/genetics*
- Female
- Fibroblast Growth Factor 3/genetics*
- Gene Deletion
- Genetic Linkage
- Humans
- Labyrinth Diseases/congenital
- Labyrinth Diseases/genetics*
- Loss of Heterozygosity
- Male
- Organogenesis/genetics
- Pedigree
- Polymorphism, Single Nucleotide*
- Stomatognathic Diseases/congenital*
- Stomatognathic Diseases/genetics*
- Syndrome
- Zebrafish/embryology
- PubMed
- 17656375 Full text @ Hum. Mol. Genet.
Citation
Gregory-Evans, C.Y., Moosajee, M., Hodges, M.D., Mackay, D.S., Game, L., Vargesson, N., Bloch-Zupan, A., Rüschendorf, F., Santos-Pinto, L., Wackens, G., and Gregory-Evans, K. (2007) SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma. Human molecular genetics. 16(20):2482-2493.
Abstract
We ascertained three different families affected with oto-dental syndrome, a rare but severe autosomal dominant craniofacial anomaly. All affected patients had the unique phenotype of grossly enlarged molar teeth (globodontia) segregating with a high frequency sensorineural hearing loss. In addition, ocular coloboma segregated with disease in one family (oculo-oto-dental syndrome). A genome-wide scan was performed using the Affymetrix GeneChip10K 2.0 Array. Parametric linkage analysis gave a single LOD score peak of 3.9 identifying linkage to chromosome 11q13. Haplotype analysis revealed three obligatory recombination events defining a 4.8 Mb linked interval between D11S1889 and SNP rs2077955. Higher resolution mapping and Southern blot analysis in each family identified overlapping hemizygous microdeletions. SNP expression analysis and real-time qRT-PCR in patient lymphoblast cell lines excluded a position effect on the flanking genes ORAOV1, PPFIA1 and CTTN. The smallest 43 kb deletion resulted in the loss of only one gene, FGF3, which was also deleted in all other otodental families. These data suggest that FGF3 haploinsufficiency is likely to be the cause of otodental syndrome. In addition, the Fas-associated death domain gene (FADD) was also deleted in the one family segregating ocular coloboma. Spatiotemporal in situ hybridisation in zebrafish embryos established for the first time that fadd is expressed during eye development. We therefore propose that FADD haploinsufficiency is likely to be responsible for ocular coloboma in this family. This study therefore implicates FGF3 and FADD in human craniofacial disease.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping