Familial short stature and intrauterine growth retardation associated with a novel mutation in the IGF-I receptor (IGF1R) gene
| Autor: | Mónica Fernández-Cancio, Antonio de Arriba, Angel Ferrández-Longás, Esteban Mayayo, A. Carrascosa, Beatriz Puga, María T. Calvo, Pilar Andaluz, Laura Audí, José I Labarta, Eva Barrio |
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| Jazyk: | angličtina |
| Rok vydání: | 2016 |
| Předmět: |
Adult
medicine.medical_specialty Microcephaly Endocrinology Diabetes and Metabolism DNA Mutational Analysis Mutation Missense Context (language use) Biology medicine.disease_cause Receptor IGF Type 1 Exon Endocrinology Pregnancy Internal medicine medicine Humans Missense mutation Genetic Predisposition to Disease Child Extracellular Signal-Regulated MAP Kinases Insulin-like growth factor 1 receptor Regulation of gene expression Mutation Fetal Growth Retardation Gene Expression Regulation Developmental DNA Middle Aged medicine.disease IGF1R Gene Pedigree body regions Female Proto-Oncogene Proteins c-akt |
| DOI: | 10.1111/j.1365-2265.2012.04481.x |
| Popis: | Summary Context IGF-I is essential for normal human growth and mediates its effects through the IGF1R. IGF1R mutations have been associated with varying degrees of intrauterine and postnatal growth retardation. Objective To identify IGF1R gene mutations in a short-statured family with intrauterine growth retardation and microcephaly. Methods Direct DNA sequencing was used to identify IGF1R mutations. Multiplex ligation-dependent probe amplification analyses were performed for deletions and duplications of all IGF1R exons. Functional studies were conducted to assess mutation pathogenicity. Results A novel heterozygous IGF1R missense mutation in exon 7 (c.A1549T, p.Y487F) was identified in a short-statured girl with severe prenatal growth retardation and microcephaly. The same mutation was also identified in her mother, who presented prenatal and postnatal growth failure, and her short-statured maternal grandmother, both of whom exhibited microcephaly. The index case showed a partial response to rhGH. Functional studies performed in dermal fibroblasts from the index case and her mother showed normal IGF-I binding; however, IGF-I activation of intracellular signalling measured as AKT and extracellular signal–regulated kinase phosphorylation was markedly reduced, with patients’ values being lower than those of her mother. IGF-I stimulation of DNA synthesis was significantly reduced compared with controls. Conclusion Our results show a novel missense mutation in the IGF1R gene (c.A1549T, p.Y487F) associated with prenatal and postnatal growth failure and microcephaly in the context of familial short stature. The functional studies are in line with the inactivation of one copy of the IGF1R gene with variable expression within the same family. |
| Databáze: | OpenAIRE |
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