Skip to main content
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1993 Oct;53(4):836–843.

Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO).

R Shiang 1, A C Lidral 1, H H Ardinger 1, K H Buetow 1, P A Romitti 1, R G Munger 1, J C Murray 1
PMCID: PMC1682388  PMID: 8105683

Abstract

Genetic analysis and tissue-specific expression studies support a role for transforming growth-factor alpha (TGFA) in craniofacial development. Previous studies have confirmed an association of alleles for TGFA with nonsyndromic cleft lip with or without cleft palate (CL/P) in humans. We carried out a retrospective association study to determine whether specific allelic variants of the TGFA gene are also associated with cleft palate only (CPO). The PCR products from 12 overlapping sets of primers to the TGFA cDNA were examined by using single-strand conformational polymorphism analysis. Four DNA polymorphic sites for TGFA were identified in the 3' untranslated region of the TGFA gene. These variants, as well as previously identified RFLPs for TGFA, were characterized in case and control populations for CPO by using chi 2 analysis. A significant association between alleles of TGFA and CPO was identified which further supports a role for this gene as one of the genetic determinants of craniofacial development. Sequence analysis of the variants disclosed a cluster of three variable sites within 30 bp of each other in the 3' untranslated region previously associated with an antisense transcript. These studies extend the role for TGFA in craniofacial morphogenesis and support an interrelated mechanism underlying nonsyndromic forms of CL/P.

Full text

PDF
836

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ardinger H. H., Buetow K. H., Bell G. I., Bardach J., VanDemark D. R., Murray J. C. Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate. Am J Hum Genet. 1989 Sep;45(3):348–353. [PMC free article] [PubMed] [Google Scholar]
  2. Bass B. L., Weintraub H. An unwinding activity that covalently modifies its double-stranded RNA substrate. Cell. 1988 Dec 23;55(6):1089–1098. doi: 10.1016/0092-8674(88)90253-x. [DOI] [PubMed] [Google Scholar]
  3. Blasband A. J., Rogers K. T., Chen X. R., Azizkhan J. C., Lee D. C. Characterization of the rat transforming growth factor alpha gene and identification of promoter sequences. Mol Cell Biol. 1990 May;10(5):2111–2121. doi: 10.1128/mcb.10.5.2111-2121.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Burdick A. B., Bixler D., Puckett C. L. Genetic analysis in families with van der Woude syndrome. J Craniofac Genet Dev Biol. 1985;5(2):181–208. [PubMed] [Google Scholar]
  5. Carter C. O. Genetics of common disorders. Br Med Bull. 1969 Jan;25(1):52–57. doi: 10.1093/oxfordjournals.bmb.a070671. [DOI] [PubMed] [Google Scholar]
  6. Chenevix-Trench G., Jones K., Green A. C., Duffy D. L., Martin N. G. Cleft lip with or without cleft palate: associations with transforming growth factor alpha and retinoic acid receptor loci. Am J Hum Genet. 1992 Dec;51(6):1377–1385. [PMC free article] [PubMed] [Google Scholar]
  7. Chenevix-Trench G., Jones K., Green A., Martin N. Further evidence for an association between genetic variation in transforming growth factor alpha and cleft lip and palate. Am J Hum Genet. 1991 May;48(5):1012–1013. [PMC free article] [PubMed] [Google Scholar]
  8. Chung C. S., Beechert A. M., Lew R. E. Test of genetic heterogeneity of cleft lip with or without cleft palate as related to race and severity. Genet Epidemiol. 1989;6(5):625–631. doi: 10.1002/gepi.1370060507. [DOI] [PubMed] [Google Scholar]
  9. Chung C. S., Bixler D., Watanabe T., Koguchi H., Fogh-Andersen P. Segregation analysis of cleft lip with or without cleft palate: a comparison of Danish and Japanese data. Am J Hum Genet. 1986 Nov;39(5):603–611. [PMC free article] [PubMed] [Google Scholar]
  10. Derynck R., Roberts A. B., Winkler M. E., Chen E. Y., Goeddel D. V. Human transforming growth factor-alpha: precursor structure and expression in E. coli. Cell. 1984 Aug;38(1):287–297. doi: 10.1016/0092-8674(84)90550-6. [DOI] [PubMed] [Google Scholar]
  11. Dixon M. J., Dixon J., Raskova D., Le Beau M. M., Williamson R., Klinger K., Landes G. M. Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2. Hum Mol Genet. 1992 Jul;1(4):249–253. doi: 10.1093/hmg/1.4.249. [DOI] [PubMed] [Google Scholar]
  12. Dixon M. J., Garner J., Ferguson M. W. Immunolocalization of epidermal growth factor (EGF), EGF receptor and transforming growth factor alpha (TGF alpha) during murine palatogenesis in vivo and in vitro. Anat Embryol (Berl) 1991;184(1):83–91. doi: 10.1007/BF01744264. [DOI] [PubMed] [Google Scholar]
  13. Driscoll D. A., Spinner N. B., Budarf M. L., McDonald-McGinn D. M., Zackai E. H., Goldberg R. B., Shprintzen R. J., Saal H. M., Zonana J., Jones M. C. Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome. Am J Med Genet. 1992 Sep 15;44(2):261–268. doi: 10.1002/ajmg.1320440237. [DOI] [PubMed] [Google Scholar]
  14. Farrall M., Buetow K. H., Murray J. C. Resolving an apparent paradox concerning the role of TGFA in CL/P. Am J Hum Genet. 1993 Feb;52(2):434–437. [PMC free article] [PubMed] [Google Scholar]
  15. Farrall M., Buetow K. H., Murray J. C. Resolving an apparent paradox concerning the role of TGFA in CL/P. Am J Hum Genet. 1993 Feb;52(2):434–437. [PMC free article] [PubMed] [Google Scholar]
  16. Farrall M., Holder S. Familial recurrence-pattern analysis of cleft lip with or without cleft palate. Am J Hum Genet. 1992 Feb;50(2):270–277. [PMC free article] [PubMed] [Google Scholar]
  17. Feinberg A. P., Vogelstein B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem. 1983 Jul 1;132(1):6–13. doi: 10.1016/0003-2697(83)90418-9. [DOI] [PubMed] [Google Scholar]
  18. Ferguson M. W. Palate development: mechanisms and malformations. Ir J Med Sci. 1987 Nov;156(11):309–315. doi: 10.1007/BF02951261. [DOI] [PubMed] [Google Scholar]
  19. Fraser F. C. The genetics of cleft lip and cleft palate. Am J Hum Genet. 1970 May;22(3):336–352. [PMC free article] [PubMed] [Google Scholar]
  20. Hecht J. T., Wang Y. P., Blanton S. H., Michels V. V., Daiger S. P. Cleft lip and palate: no evidence of linkage to transforming growth factor alpha. Am J Hum Genet. 1991 Sep;49(3):682–686. [PMC free article] [PubMed] [Google Scholar]
  21. Hecht J. T., Yang P., Michels V. V., Buetow K. H. Complex segregation analysis of nonsyndromic cleft lip and palate. Am J Hum Genet. 1991 Sep;49(3):674–681. [PMC free article] [PubMed] [Google Scholar]
  22. Holder S. E., Vintiner G. M., Farren B., Malcolm S., Winter R. M. Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palate. J Med Genet. 1992 Jun;29(6):390–392. doi: 10.1136/jmg.29.6.390. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Hästbacka J., Kaitila I., Sistonen P., de la Chapelle A. Diastrophic dysplasia gene maps to the distal long arm of chromosome 5. Proc Natl Acad Sci U S A. 1990 Oct;87(20):8056–8059. doi: 10.1073/pnas.87.20.8056. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Jakobovits E. B., Schlokat U., Vannice J. L., Derynck R., Levinson A. D. The human transforming growth factor alpha promoter directs transcription initiation from a single site in the absence of a TATA sequence. Mol Cell Biol. 1988 Dec;8(12):5549–5554. doi: 10.1128/mcb.8.12.5549-5554.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Jakowlew S. B., Kondaiah P., Dillard P. J., Sporn M. B., Roberts A. B. A novel low molecular weight ribonucleic acid (RNA) related to transforming growth factor alpha messenger RNA. Mol Endocrinol. 1988 Nov;2(11):1056–1063. doi: 10.1210/mend-2-11-1056. [DOI] [PubMed] [Google Scholar]
  26. Marazita M. L., Hu D. N., Spence M. A., Liu Y. E., Melnick M. Cleft lip with or without cleft palate in Shanghai, China: evidence for an autosomal major locus. Am J Hum Genet. 1992 Sep;51(3):648–653. [PMC free article] [PubMed] [Google Scholar]
  27. Marchuk D., Drumm M., Saulino A., Collins F. S. Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products. Nucleic Acids Res. 1991 Mar 11;19(5):1154–1154. doi: 10.1093/nar/19.5.1154. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Melnick M. Cleft lip (+/- cleft palate) etiology: a search for solutions. Am J Med Genet. 1992 Jan 1;42(1):10–14. doi: 10.1002/ajmg.1320420104. [DOI] [PubMed] [Google Scholar]
  29. Moore G. E., Ivens A., Chambers J., Farrall M., Williamson R., Page D. C., Bjornsson A., Arnason A., Jensson O. Linkage of an X-chromosome cleft palate gene. Nature. 1987 Mar 5;326(6108):91–92. doi: 10.1038/326091a0. [DOI] [PubMed] [Google Scholar]
  30. Morell R., Friedman T. B., Moeljopawiro S., Hartono, Soewito, Asher J. H., Jr A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian family. Hum Mol Genet. 1992 Jul;1(4):243–247. doi: 10.1093/hmg/1.4.243. [DOI] [PubMed] [Google Scholar]
  31. Murray J. C., Bennett S. R., Kwitek A. E., Small K. W., Schinzel A., Alward W. L., Weber J. L., Bell G. I., Buetow K. H. Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4. Nat Genet. 1992 Sep;2(1):46–49. doi: 10.1038/ng0992-46. [DOI] [PubMed] [Google Scholar]
  32. Murray J. C., DeHaven C. R., Bell G. I. RFLPs for epidermal growth factor (EGF), a single copy sequence at 4q25-4q27. Nucleic Acids Res. 1986 Jun 25;14(12):5117–5117. doi: 10.1093/nar/14.12.5117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Murray J. C., Nishimura D. Y., Buetow K. H., Ardinger H. H., Spence M. A., Sparkes R. S., Falk R. E., Falk P. M., Gardner R. J., Harkness E. M. Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq. Am J Hum Genet. 1990 Mar;46(3):486–491. [PMC free article] [PubMed] [Google Scholar]
  34. Orita M., Suzuki Y., Sekiya T., Hayashi K. Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. Genomics. 1989 Nov;5(4):874–879. doi: 10.1016/0888-7543(89)90129-8. [DOI] [PubMed] [Google Scholar]
  35. Poncz M., Solowiejczyk D., Harpel B., Mory Y., Schwartz E., Surrey S. Construction of human gene libraries from small amounts of peripheral blood: analysis of beta-like globin genes. Hemoglobin. 1982;6(1):27–36. doi: 10.3109/03630268208996930. [DOI] [PubMed] [Google Scholar]
  36. Sassani R., Bartlett S. P., Feng H., Goldner-Sauve A., Haq A. K., Buetow K. H., Gasser D. L. Association between alleles of the transforming growth factor-alpha locus and the occurrence of cleft lip. Am J Med Genet. 1993 Mar 1;45(5):565–569. doi: 10.1002/ajmg.1320450508. [DOI] [PubMed] [Google Scholar]
  37. Sheffield V. C., Beck J. S., Nichols B., Cousineau A., Lidral A. C., Stone E. M. Detection of multiallele polymorphisms within gene sequences by GC-clamped denaturing gradient gel electrophoresis. Am J Hum Genet. 1992 Mar;50(3):567–575. [PMC free article] [PubMed] [Google Scholar]
  38. Stoll C., Qian J. F., Feingold J., Sauvage P., May E. Genetic variation in transforming growth factor alpha: possible association of BamHI polymorphism with bilateral sporadic cleft lip and palate. Am J Hum Genet. 1992 Apr;50(4):870–871. [PMC free article] [PubMed] [Google Scholar]
  39. Vintiner G. M., Holder S. E., Winter R. M., Malcolm S. No evidence of linkage between the transforming growth factor-alpha gene in families with apparently autosomal dominant inheritance of cleft lip and palate. J Med Genet. 1992 Jun;29(6):393–397. doi: 10.1136/jmg.29.6.393. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Wagner R. W., Smith J. E., Cooperman B. S., Nishikura K. A double-stranded RNA unwinding activity introduces structural alterations by means of adenosine to inosine conversions in mammalian cells and Xenopus eggs. Proc Natl Acad Sci U S A. 1989 Apr;86(8):2647–2651. doi: 10.1073/pnas.86.8.2647. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Willing M. C., Pruchno C. J., Atkinson M., Byers P. H. Osteogenesis imperfecta type I is commonly due to a COL1A1 null allele of type I collagen. Am J Hum Genet. 1992 Sep;51(3):508–515. [PMC free article] [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES