Skip to main content
Journal of Clinical Laboratory Analysis logoLink to Journal of Clinical Laboratory Analysis
. 2006 Jul 27;20(4):133–138. doi: 10.1002/jcla.20121

Crossed polydactyly type I caused by a point mutation in the GLI3 gene in a large Chinese pedigree

Baowen Cheng 1, Yongli Dong 1, Li He 1, Wenru Tang 1, Haijing Yu 1, Jing Lu 1, Lin Xu 1, Bingrong Zheng 1, Kaiyuan Li 1, Chunjie Xiao 1,
PMCID: PMC6807395  PMID: 16874813

Abstract

Polydactyly is one of the most common forms of congenital malformation in humans, and is displayed by 119 disorders. Crossed polydactyly (CP) is defined as the coexistence of preaxial and postaxial polydactyly with a difference in the axes of polydactyly between the hands and feet. In an effort to map the gene responsible for CP, we studied a seven‐generation Chinese family of 56 individuals, 28 of whom were affected. A thorough search with highly informative polymorphic markers showed no recombination among the affected members with the markers on chromosome 7p15‐q11.23, but no linkage with chromosomes 2q31, 7q36, 13q, and 19p. Mutation analysis showed a substitution mutation of 1927C → T in exon 12 of the GLI3 gene, which is predicted to pretruncate the GLI3 protein. This mutation has variable phenotypes of polydactyly, indicating that other genetic factors also contribute to the diversity of polydactyly phenotypes. Our results increase the phenotypic spectrum caused by GLI3 mutations and are important for the analysis and understanding of the etiology of these limb malformations. J. Clin. Lab. Anal. 20:133–138, 2006. © 2006 Wiley‐Liss, Inc.

Keywords: linkage, chromosome 7p15‐q11.23, limb development, truncated protein

REFERENCES

  • 1. Biesecker LG. Poydactyly: how many disorders and how many genes? Am J Med Genet 2002;112:279–283. [DOI] [PubMed] [Google Scholar]
  • 2. Giorgini MJ, Kass AA, Sollitto RJ, Midenberg ML. Crossed polydactyly: a case report. J Foot Surg 1979;18:159–163. [Google Scholar]
  • 3. Muragaki Y, Mundlos S, Upton J, Olsen BR. Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13 . Science 1996;272:548–551. [DOI] [PubMed] [Google Scholar]
  • 4. Sarfarazi M, Akarsu AN, Sayli BS. Localization of the syndactyly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker. Hum Mol Genet 1995;4:1453–1458. [DOI] [PubMed] [Google Scholar]
  • 5. Heus HG, Hing A, Van Baren MJ, Joosse M. A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36. Genomics 1999;57:342–351. [DOI] [PubMed] [Google Scholar]
  • 6. Akarsu AN, Ozbas F, Kostakoglu N. Mapping of the second locus of postaxial polydactyly type A (PAP‐A2) to chromosome 13q21‐q32. Am J Hum Genet 1997;61(Suppl):A265. [Google Scholar]
  • 7. Zhao H, Tian Y, Guido B, Breedveld G, Huang S, Zou Y, Jue Y. Postaxial polydactyly type A/B(PAP‐A/B) is linked to chromosome 19p13.1‐13.2 in a Chinese kindred. Eur J Hum Genet 2002;10:162–166. [DOI] [PubMed] [Google Scholar]
  • 8. Dominguez M, Brunner M, Hafen E, Basler K. Sending and receiving the hedgehog signal: control by the Drosophila GLI protein Cubitus interruptus. Science 1996;272:1621–1625. [DOI] [PubMed] [Google Scholar]
  • 9. Welscher PT, Zuniga A, Kuijper S, et al. Progression of vertebrate limb development through Shh‐mediated counteraction of GLI3. Science 2002;298:827–830. [DOI] [PubMed] [Google Scholar]
  • 10. Litingtung Y, Dahn RD, Li Y, Fallon JF, Chiang C. Shh and Gli3 are dispensable for limb skeleton formation but regulate digit number and identity. Nature 2002;418:979–983. [DOI] [PubMed] [Google Scholar]
  • 11. Wild A, Kalff‐Suske M, Vortkamp A, Bornholdt D, Koning R, Grzeschik KH. Point mutation in human GLI3 causes Greig syndrome. Hum Mol Genet 1997;6:1979–1984. [DOI] [PubMed] [Google Scholar]
  • 12. Kang S, Graham JMJ, Olney AH, Biesecker LG. GLI3 frameshift mutations cause autosomal dominant Pallister‐Hall syndrome. Nat Genet 1997;15:266–268. [DOI] [PubMed] [Google Scholar]
  • 13. Radhakrishna U, Blouin J, Mehenni H, et al. Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15‐q11.23 by linkage analysis. Am J Hum Genet 1997;60:597–604. [PMC free article] [PubMed] [Google Scholar]
  • 14. Radhakrishna U, Bornholdt D, Scott HS. The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type‐IV and postaxial polydactyly type‐A/B: no phenotype prediction from the position of GLI3 mutations. Am J Hum Genet 1999;65:645–655. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Gross‐Bellard M, Oudet P, Chambon P. Isolation of high molecular weight DNA from mammalian cells. Eur J Biochem 1973;36:32–38. [DOI] [PubMed] [Google Scholar]
  • 16. Cheng B, Cheng G, Zhang H. A study of forensic individual identification used PCR locus with silver staining and multiplex PCR methods. Hereditas (Beijing) 2002;24:15–18. [PubMed] [Google Scholar]
  • 17. Mathrop GM, Lalouel JM, Julier C, Ott J. Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci USA 1984;81:3443–3446. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18. Kang S, Rosenberg M, Ko VD, Biesecker LG. Gene structure and allelic expression assay of the human GLI3 gene. Hum Genet 1997;101:154–157. [DOI] [PubMed] [Google Scholar]
  • 19. Ishikiriyama S, Sawada H, Nambu H, Nikawa N. Crossed polydactyly type I in a mother and son: an autosomal dominant trait? Am J Med Genet 1991;40:41–43. [DOI] [PubMed] [Google Scholar]
  • 20. Johnston JJ, Olivos‐Glander I, Killoran C, et al. Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister‐Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations. Am J Hum Genet 2005;76:609–622. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Lettice LA, Horikoshi T, Heaney SJH, Van Baren MJ. Disruption of a long‐range cis‐acting regulator for SHH causes preaxial polydactyly. Proc Natl Acad Sci USA 2002;99:7548–7553. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Clinical Laboratory Analysis are provided here courtesy of Wiley

RESOURCES