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1.
J Biol Chem ; 287(45): 37926-38, 2012 Nov 02.
Artículo en Inglés | MEDLINE | ID: mdl-22988238

RESUMEN

Testis differentiation in zebrafish involves juvenile ovary to testis transformation initiated by an apoptotic wave. The molecular regulation of this transformation process is not fully understood. NF-κB is activated at an early stage of development and has been shown to interact with steroidogenic factor-1 in mammals, leading to the suppression of anti-Müllerian hormone (Amh) gene expression. Because steroidogenic factor-1 and Amh are important for proper testis development, NF-κB-mediated induction of anti-apoptotic genes could, therefore, also play a role in zebrafish gonad differentiation. The aim of this study was to examine the potential role of NF-κB in zebrafish gonad differentiation. Exposure of juvenile zebrafish to heat-killed Escherichia coli activated the NF-κB pathways and resulted in an increased ratio of females from 30 to 85%. Microarray and quantitative real-time-PCR analysis of gonads showed elevated expression of NF-κB-regulated genes. To confirm the involvement of NF-κB-induced anti-apoptotic effects, zebrafish were treated with sodium deoxycholate, a known inducer of NF-κB or NF-κB activation inhibitor (NAI). Sodium deoxycholate treatment mimicked the effect of heat-killed bacteria and resulted in an increased proportion of females from 25 to 45%, whereas the inhibition of NF-κB using NAI resulted in a decrease in females from 45 to 20%. This study provides proof for an essential role of NF-κB in gonadal differentiation of zebrafish and represents an important step toward the complete understanding of the complicated process of sex differentiation in this species and possibly other cyprinid teleosts as well.


Asunto(s)
FN-kappa B/metabolismo , Ovario/crecimiento & desarrollo , Testículo/crecimiento & desarrollo , Proteínas de Pez Cebra/metabolismo , Pez Cebra/metabolismo , Animales , Apoptosis/efectos de los fármacos , Apoptosis/genética , Western Blotting , Línea Celular , Ácido Desoxicólico/farmacología , Escherichia coli/inmunología , Femenino , Perfilación de la Expresión Génica , Redes Reguladoras de Genes , Calor , Masculino , Modelos Genéticos , FN-kappa B/antagonistas & inhibidores , FN-kappa B/genética , Análisis de Secuencia por Matrices de Oligonucleótidos , Ovario/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Diferenciación Sexual/efectos de los fármacos , Diferenciación Sexual/genética , Transducción de Señal/efectos de los fármacos , Transducción de Señal/genética , Testículo/metabolismo , Transcriptoma/genética , Transcriptoma/inmunología , Pez Cebra/genética , Pez Cebra/inmunología , Proteínas de Pez Cebra/antagonistas & inhibidores , Proteínas de Pez Cebra/genética
2.
Artículo en Inglés | MEDLINE | ID: mdl-18950725

RESUMEN

The NR5A family of orphan nuclear receptors has been implicated in development of the vertebrate embryo, but their exact role remains largely unknown. To evaluate the regulation and developmental role for ff1a (NR5A2) in zebrafish (Danio rerio), we performed morpholino knockdown to block translation of the ff1a gene and the upstream located sox9a gene during embryogenesis. Using a newly developed antibody against Ff1a we could show that the ff1a morpholinos were functional and that a reduction in the expression of Ff1a correlated to altered phenotypes. The role of Sox9a in ff1a gene regulation and function was studied using sox9a morpholinos. Knock-down of sox9a resulted in abolished ff1a signals in the somites, mandibular arches and pharyngeal arches, while the pectoral fin signal remained. The reduction in Ff1a levels correlated to truncated tails and cranio-facial malformation. As Sox9a is involved in chondrocyte development we analysed for cartilage formation and found that blocking translation of either sox9a or ff1a also blocked cartilage formation. In light of the results, the present study suggests a novel function of ff1a in chondrocyte development.


Asunto(s)
Cartílago/embriología , Receptores Citoplasmáticos y Nucleares/metabolismo , Factor de Transcripción SOX9/metabolismo , Proteínas de Pez Cebra/metabolismo , Pez Cebra/embriología , Azul Alcián , Animales , Western Blotting , Cartílago/metabolismo , Embrión no Mamífero/metabolismo , Regulación del Desarrollo de la Expresión Génica , Gónadas/metabolismo , Hibridación in Situ , Hígado/metabolismo , ARN Mensajero/genética , ARN Mensajero/metabolismo , Receptores Citoplasmáticos y Nucleares/genética , Factor de Transcripción SOX9/genética , Pez Cebra/genética , Proteínas de Pez Cebra/genética
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