RESUMO
The whirler mouse mutant (wi) does not respond to sound stimuli, and detailed ultrastructural analysis of sensory hair cells in the organ of Corti of the inner ear indicates that the whirler gene encodes a protein involved in the elongation and maintenance of stereocilia in both inner hair cells (IHCs) and outer hair cells (OHCs). BAC-mediated transgene correction of the mouse phenotype and mutation analysis identified the causative gene as encoding a novel PDZ protein called whirlin. The gene encoding whirlin also underlies the human autosomal recessive deafness locus DFNB31. In the mouse cochlea, whirlin is expressed in the sensory IHC and OHC stereocilia. Our findings suggest that this novel PDZ domain-containing molecule acts as an organizer of submembranous molecular complexes that control the coordinated actin polymerization and membrane growth of stereocilia.
Assuntos
Surdez/genética , Expressão Gênica , Proteínas de Membrana/genética , Proteínas/genética , Sequência de Aminoácidos , Animais , Mapeamento Cromossômico , Cílios/fisiologia , Cílios/ultraestrutura , Análise Mutacional de DNA , DNA Complementar/genética , Genes Recessivos , Células Ciliadas Auditivas Internas/ultraestrutura , Células Ciliadas Auditivas Externas/ultraestrutura , Humanos , Proteínas de Membrana/fisiologia , Camundongos , Camundongos Mutantes , Camundongos Transgênicos , Dados de Sequência Molecular , Fenótipo , Proteínas/fisiologia , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Homologia de Sequência de Aminoácidos , Especificidade da EspécieRESUMO
Otitis media (OM), inflammation of the middle ear, remains the most common cause of hearing impairment in children. It is also the most common cause of surgery in children in the developed world. There is evidence from studies of the human population and mouse models that there is a significant genetic component predisposing to OM, yet nothing is known about the underlying genetic pathways involved in humans. We identified an N-ethyl-N-nitrosourea-induced dominant mouse mutant Junbo with hearing loss due to chronic suppurative OM and otorrhea. This develops from acute OM that arises spontaneously in the postnatal period, with the age of onset and early severity dependent on the microbiological status of the mice and their air quality. We have identified the causal mutation, a missense change in the C-terminal zinc finger region of the transcription factor Evi1. This protein is expressed in middle ear basal epithelial cells, fibroblasts, and neutrophil leukocytes at postnatal day 13 and 21 when inflammatory changes are underway. The identification and characterization of the Junbo mutant elaborates a novel role for Evi1 in mammalian disease and implicates a new pathway in genetic predisposition to OM.
Assuntos
Proteínas de Ligação a DNA/genética , Predisposição Genética para Doença/genética , Mutação/genética , Otite Média/genética , Proto-Oncogenes/genética , Fatores de Transcrição/genética , Sequência de Aminoácidos , Animais , Mapeamento Cromossômico , Clonagem Molecular , Análise Mutacional de DNA , Proteínas de Ligação a DNA/química , Orelha Média/citologia , Orelha Média/patologia , Citometria de Fluxo , Granulócitos/imunologia , Pulmão/citologia , Pulmão/patologia , Proteína do Locus do Complexo MDS1 e EVI1 , Masculino , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Mutantes , Dados de Sequência Molecular , Nariz/citologia , Nariz/patologia , Otite Média/imunologia , Fenótipo , Organismos Livres de Patógenos Específicos , Fatores de Transcrição/químicaRESUMO
N-ethyl-N-nitrosourea (ENU) introduces mutations throughout the mouse genome at relatively high efficiency. Successful high-throughput phenotype screens have been reported and alternative screens using sequence-based approaches have been proposed. For the purpose of generating an allelic series in selected genes by a sequence-based approach, we have constructed an archive of over 4000 DNA samples from individual F1 ENU-mutagenized mice paralleled by frozen sperm samples. Together with our previously reported archive, the total size now exceeds 6000 individuals. A gene-based screen of 27.4 Mbp of DNA, carried out using denaturing high-performance liquid chromatography (DHPLC), found a mutation rate of 1 in 1.01 Mbp of which 1 in 1.82 Mbp were potentially functional. Screening of whole or selected regions of genes on subsets of the archive has allowed us to identify 15 new alleles from 9 genes out of 15 tested. This is a powerful adjunct to conventional mutagenesis strategies and has the advantage of generating a variety of alleles with potentially different phenotypic outcomes that facilitate the investigation of gene function. It is now available to academic collaborators as a community resource.