A novel TGM1 mutation, leading to multiple splicing rearrangements, is associated with autosomal recessive congenital ichthyosis
Summary Autosomal recessive congenital ichthyosis (ARCI) is a group of rare, clinically heterogeneous skin disorders that affect cornification. ARCI includes lamellar ichthyosis, congenital ichthyosiform erythroderma and harlequin ichthyosis. TGM1 mutations cause > 50% of ARCI cases in the USA. W...
| Autores: | , , , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2015 |
| País: | Colombia |
| Institución: | Universidad del Rosario |
| Repositorio: | Repositorio EdocUR - U. Rosario |
| Idioma: | inglés |
| OAI Identifier: | oai:repository.urosario.edu.co:10336/23667 |
| Acceso en línea: | https://doi.org/10.1111/ced.12627 https://repository.urosario.edu.co/handle/10336/23667 |
| Access Level: | acceso abierto |
| Palabra clave: | Adult Amplicon Article Autosomal recessive congenital ichthyosis Case report Exon skipping Female Gene Gene mutation Gene rearrangement Genetic counseling Genotype Genotype phenotype correlation Human Ichthyosis Intron Intron retention Phenotype Physical examination Priority journal Single nucleotide polymorphism Stop codon Tgm1 gene Congenital ichthyosiform erythroderma Genetic predisposition Genetics Mutation Recessive gene Rna splicing Protein glutamine gamma glutamyltransferase Transglutaminase 1 Genetic predisposition to disease Humans Rna splice sites Transglutaminases congenital recessive Genes Ichthyosiform erythroderma |
| Sumario: | Summary Autosomal recessive congenital ichthyosis (ARCI) is a group of rare, clinically heterogeneous skin disorders that affect cornification. ARCI includes lamellar ichthyosis, congenital ichthyosiform erythroderma and harlequin ichthyosis. TGM1 mutations cause > 50% of ARCI cases in the USA. We report two siblings with ARCI. They were found to carry a novel aetiological TGM1 mutation, which leads to the synthesis of multiple abnormal transcripts. These molecules resulted from three independent mechanisms: intron retention, exon skipping and activation of expand cryptic splice sites. Taken together, our findings expand the known TGM1 mutation repertoire, and provide an insight into the molecular mechanisms leading to ARCI phenotypes. These results could be useful for genetic counselling and future potential genotype-phenotype correlations. © 2015 British Association of Dermatologists. |
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