Clefts of the lip and palate (CLP) are one of the most common craniofacial anomalies, with a rate of 1:650 in the United States population. Over 250 genetically based syndromes exist which include cleft lip or palate as a feature of their clinical presentation. Since the fall of 1993, we have been collaborating with the Lancaster Cleft Palate Clinic in Lancaster, PA. This project is a large-scale molecular epidemiological study, involving the comprehensive mapping of highly informative DNA markers, utilizing the clinical population from the Lancaster Cleft Palate Clinic and affiliated clinics. In the past year we completed recruitment efforts at Washington University, St. Louis and at the University of North Carolina, Chapel Hill. Semiautomated gene mapping technologies developed by our group in ongoing CLP studies are being applied to map genes responsible for clefting. We are currently completing the first phase of statistical analyses of both our genome scan and candidate region gene mapping data. Results of these data analyses were presented to the Board of Scientific Counselors at our June review. Two analytical strategies are being employed: case-sibling control analysis to evaluate gene-disease associations and gene-environment interactions, and linkage disequilibrium and linkage analyses to identify chromosomal locations associated with susceptibility to non-syndromic oral clefts. For the case-sibling control analysis, a variation of the generalized estimating equation (GEE) method is being developed by our group. This approach will allow for the control of correlated variables while performing regression analyses. Candidate genes and chromosomal regions that will be tested using this approach include SNPs and flanking markers for Methylenetetrahydrofolate Reductase on chromosome 1, Transforming Growth Factor Alpha on chromosome 2, MSX1 on chromosome 4p, regions on 4q where possible linkage and a deletion associated with clefting have been reported, F13A on chromosome 6, Transforming Growth factor Beta 3 on chromosome 14, D17S579, BCL3 on chromosome 19, and D22S264. Environmental risk factors that will be included in the models are maternal use of tobacco, alcohol, multivitamins and medications, diseases during pregnancy, and family history of any birth defect. The linkage disequilibrium and linkage analyses component of this research effort involves use of numerous complex statistical methods applied to the candidate genes and chromosomal regions as well as all genome scan marker loci. These methods include Transmission Disequilibrium Tests (TDT) on case-parent triads, two-point sib-pair analyses, with covariates, with and without constraints, non-parametric linkage analysis for extended pedigrees, and two-point and multipoint LOD score analysis, including the admixture test for linkage in the presence of locus heterogeneity. Van der Woude syndrome is an autosomal dominant craniofacial disorder with high penetrance and variable expression of its clinical features of cleft lip and/or cleft palate, lip pits and hypodontia. A gene which causes this disease has been localized to a < 2 cM region on the long arm of chromosome 1q32. All VWS families studied previously are linked to this region (i.e., locus homogeneity).
The aim of our study was to refine the localization of the VWS gene and to further assess possible locus heterogeneity. We recruited four multiplex VWS families in collaboration with Drs. Mazaheri and Long of the Lancaster Cleft Palate Clinic, Dr. Soraya Beiraghi of the University of Nebraska Medical Center and Dr. Robert P. Erickson of the University of Arizona Health Science Center. We used automated genotyping methods to characterize 19 STR markers on chromosome 1 in the VWS candidate gene region. We performed two point and multi point LODs core analyses using a high penetrance autosomal dominant mode l. All families show positive LOD scores without any recombination in the candidate region. The largest two point LOD score was 5.87. Our results are fully consistent with previous mapping of the VWS gene between D1S491 and D1S205. Our assay method for STR markers provided highly accurate size estimation of marker allele fragment sizes and, therefore, enabled us to determine the specific alleles segregating with the VWS gene in each of our four families. We observed a striking pattern of STR allele sharing at several closely linked loci among our four Caucasian VWS families recruited at three different locations in the U.S. This suggests the possibility of a unique origin for a mutation responsible for many or most cases of VWS. If confirmed in other families, linkage disequilibrium may be helpful for fine mapping of the location of the VWS disease gene to facilitate its cloning. In collaboration with Dr. Robert P. Erickson of the University of Arizona Health Sciences Center, we statistically analyzed a teratogen-induced mouse model of oral cleft susceptibility using recombinant inbred lines and genetic markers covering the entire mouse genome. A new statistical method for gene mapping of discrete traits (affected versus unaffected) was developed for this study, analogous to Quantitative Trait Locus (QTL) mapping of continuous traits. Several chromosomes and genes were identified that can now be used as candidates for evaluation in humans. These data also suggest that some genes influence both cleft lip and cleft palate susceptibility. A new research initiative, the Genetics of Pain, was established to explore opportunities to identify genetic polymorphisms, environmental factors, and gene-environment interactions associated with the mechanisms and perception of pain. Following discussions last summer with Dr. Mitchell Max of the Pain and Neurosensory Mechanisms Branch of the NIDCR and Dr. Zeev Seltzer from the Faculties of Medicine and Dental Medicine of Hebrew University of Jerusalem, Israel, Dr. Diehl agreed to contribute his human gene mapping expertise for two initial studies of the genetics of pain. Dr. Diehl and his staff have co-hosted Dr. Seltzer during his sabbatical at the NIDCR, providing laboratory training, advice on experimental design and statistical analysis for human and animal studies of the genetics of pain. A final section of note concerns the immotile cilia syndromes, (ICS) which are a genetically determined set of disorders characterized by dysmotility or immotility of the cilia in airway epithelial cells, spermatozoa and other ciliated cells of the body. Kartagener syndrome (KS) is a subgroup of ICS characterized by a classic triad of symptoms: situs inversus, bronchiectasis and chronic sinusitis. Ciliary immotility is caused by various ultrastructural defects of cilia, predominantly by a lack of dynein arms. The clinical consequences of KS include pronounced craniofacial manifestations.
| Wyszynski, D F; Diehl, S R (2001) The mother-only method (MOM) to detect maternal gene--environment interactions. Paediatr Perinat Epidemiol 15:317-8 |
| Wyszynski, D F; Diehl, S R (2000) Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and risk of nonsyndromic cleft lip. Am J Med Genet 92:79-80 |
