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1.
Chem Senses ; 482023 01 01.
Artigo em Inglês | MEDLINE | ID: mdl-37843175

RESUMO

The senses of taste and smell detect overlapping sets of chemical compounds in fish, e.g. amino acids are detected by both senses. However, so far taste and smell organs appeared morphologically to be very distinct, with a specialized olfactory epithelium for detection of odors and taste buds located in the oral cavity and lip for detection of tastants. Here, we report dense clusters of cells expressing T1R and T2R receptors as well as their signal transduction molecule PLCß2 in nostrils of zebrafish, i.e. on the entrance funnel through which odor molecules must pass to be detected by olfactory sensory neurons. Quantitative evaluation shows the density of these chemosensory cells in the nostrils to be as high or higher than that in the established taste organs oral cavity and lower lip. Hydrodynamic flow is maximal at the nostril rim enabling high throughput chemosensation in this organ. Taken together, our results suggest a sentinel function for these chemosensory cells in the nostril.


Assuntos
Papilas Gustativas , Peixe-Zebra , Animais , Peixe-Zebra/metabolismo , Olfato/fisiologia , Paladar/fisiologia , Fosfolipase C beta/metabolismo , Papilas Gustativas/metabolismo
2.
Neurobiol Aging ; 36(4): 1764.e9-1764.e18, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-25681989

RESUMO

The frequency of amyotrophic lateral sclerosis (ALS) mutations has been extensively investigated in several populations; however, a systematic analysis in Turkish cases has not been reported so far. In this study, we screened 477 ALS patients for mutations, including 116 familial ALS patients from 82 families and 361 sporadic ALS (sALS) cases. Patients were genotyped for C9orf72 (18.3%), SOD1 (12.2%), FUS (5%), TARDBP (3.7%), and UBQLN2 (2.4%) gene mutations, which together account for approximately 40% of familial ALS in Turkey. No SOD1 mutations were detected in sALS patients; however, C9orf72 (3.1%) and UBQLN2 (0.6%) explained 3.7% of sALS in the population. Exome sequencing revealed mutations in OPTN, SPG11, DJ1, PLEKHG5, SYNE1, TRPM7, and SQSTM1 genes, many of them novel. The spectrum of mutations reflect both the distinct genetic background and the heterogeneous nature of the Turkish ALS population.


Assuntos
Esclerose Lateral Amiotrófica/genética , Estudos de Associação Genética , Mutação/genética , Proteínas/genética , Proteína FUS de Ligação a RNA/genética , Superóxido Dismutase/genética , Proteínas Adaptadoras de Transdução de Sinal/genética , Adolescente , Adulto , Idoso , Proteínas Relacionadas à Autofagia , Proteína C9orf72 , Proteínas de Ciclo Celular/genética , Proteínas do Citoesqueleto , Proteínas de Ligação a DNA/genética , Exoma/genética , Feminino , Fatores de Troca do Nucleotídeo Guanina/genética , Humanos , Peptídeos e Proteínas de Sinalização Intracelular/genética , Masculino , Proteínas de Membrana Transportadoras , Pessoa de Meia-Idade , Proteínas do Tecido Nervoso/genética , Proteínas Nucleares/genética , Proteínas Oncogênicas/genética , Proteína Desglicase DJ-1 , Proteínas Serina-Treonina Quinases/genética , Proteína Sequestossoma-1 , Superóxido Dismutase-1 , Canais de Cátion TRPM/genética , Fator de Transcrição TFIIIA/genética , Turquia , Ubiquitinas/genética , Adulto Jovem
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