Association between alleles of the transforming growth factor-alpha locus and the occurrence of cleft lip
β Scribed by Sassani, Russell ;Bartlett, Scott P. ;Feng, Hongshu ;Goldner-Sauve, Audrey ;Haq, Asifa K. ;Buetow, Kenneth H. ;Gasser, David L.
- Book ID
- 102702158
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 699 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
β¦ Synopsis
DNA samples from 100 patients with cleft lip with or without cleft palate (CLIP) were compared with those of 98 unaffected control individuals with respect to transforming growth factor alpha (TGFA) genotypes. Among the Caucasians i n this population (83 CLIP, 84 controls), there was a significant difference in the restriction fragment length polymorphisms (RFLPs) observed after digestion with TaqI (x2 = 4.68, P = 0.03). The frequency of the C2 allele in the Caucasian CL/P population was 0.169, whereas that in the control group was 0.089. When the data for Caucasians, African-Americans, and Asians were examined jointly, the x2 value for the pooled sample was 5.08 ( P = 0.02). This confirms the hypothesis of Ardinger et al. 11989, Am J Hum Genet, 45348-3531 that TFGA itself or a closely linked gene contributes to the development of CL/P in humans. o 1993 wiley-Liss, Inc.
π SIMILAR VOLUMES
Cleft lip with or without cleft palate (CL +/- P) is the most frequent craniofacial malformation in different human populations and its cause is largely unknown. Several studies based on population associations have suggested that an allele mapping in the transforming growth factor alpha locus could
Transforming growth factor-alpha (TGFβ£) is an epidermal growth factor receptor (EGFR) ligand which is distinguished from EGF by its acid-labile structure and potent transforming function. We recently reported that TGFβ£ induces less efficient EGFR heterodimerization and downregulation than does EGF (