Mutational analysis of the Sonic Hedgehog gene in 220 newborns with oral clefts in a South American (ECLAMC) population†
- 4 January 2002
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 108 (1) , 12-15
- https://doi.org/10.1002/ajmg.10204
Abstract
Oral clefts generally have a multifactorial etiology. A number of genes contribute to the formation of the face and palate. Cleft lip and/or palate can occur in pedigrees with autosomal dominant holoprosencephaly due to mutations in Sonic Hedgehog (SHH). In addition, animal models have shown that SHH is involved in face development. We thus examined the human SHH gene in 220 newborn infants with nonsyndromic oral clefts registered by the Estudio Colaborativo Latinoamericano de Malformaciones Congenitas: ECLAMC (Latin American Collaborative Study of Congenital Malformations). We found 15 variant bands in 13 patients with oral clefts, representing five different base changes, all of which were found by sequencing to represent silent polymorphisms. Four occurred in introns. The alteration occurring in an exon, Ser190Ser, may create a consensus sequence for the 3′splice site 6 bp downstream of the original consensus sequence. Thus, we did not identify any clearly disease‐causing mutation in SHH in these patients, and conclude that SHH mutations are not a frequent cause of isolated oral clefts in humans. Published 2002 Wiley‐Liss, Inc.Keywords
Funding Information
- NIH and the Division of Intramural Research (HD01218, HD29862)
- CNPq, Brazil (200728/98-9)
- FAPERJ, Brazil (E-26/170.688/97, E-26/170.442/99)
- FUJB, Brazil (8222-8)
- CAPES, Brazil
- PAPES, Fiocruz, Brazil
- ANPICT, Argentina (PICT 4495)
This publication has 18 references indexed in Scilit:
- Identification of novel mutations in SHH and ZIC2 in a South American (ECLAMC) population with holoprosencephalyHuman Genetics, 2001
- Holoprosencephaly: Molecular study of a California PopulationAmerican Journal of Medical Genetics, 2000
- The Mutational Spectrum of the Sonic Hedgehog Gene in Holoprosencephaly: SHH Mutations Cause a Significant Proportion of Autosomal Dominant HoloprosencephalyHuman Molecular Genetics, 1999
- Expression of the Sonic hedgehog (SHH) Gene during Early Human Development and Phenotypic Expression of New Mutations Causing HoloprosencephalyHuman Molecular Genetics, 1999
- Association of MSX1 and TGFB3 with Nonsyndromic Clefting in HumansAmerican Journal of Human Genetics, 1998
- Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene functionNature, 1996
- Initial splice-site recognition and pairing during pre-mRNA splicingCurrent Opinion in Genetics & Development, 1996
- Heterogeneous rates for birth defects in Latin America: Hints on causalityGenetic Epidemiology, 1996
- Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity.Proceedings of the National Academy of Sciences, 1994
- The Surveillance of Birth Defects in South America: I. The Search for Time Clusters: EpidemicsPublished by Springer Nature ,1990