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1.
Fish Shellfish Immunol ; 84: 1145-1156, 2019 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-30408600

RESUMEN

The Nile tilapia, Oreochromis niloticus, is a species of high economic value and extensively cultured. The limited stress tolerance of this species to a low temperature usually leads to mass mortality and great loss. Nevertheless, there is limited information on the molecular mechanisms underlying the susceptibility to low temperature in the tilapia. In this study, tilapia was treated at 28 °C to a lethal temperature of 8 °C by a gradual decrement. Transcriptomic response of the immune organ, kidney, in tilapia was characterized using RNA-seq. In total, 2191 genes were annotated for significant expression, which were mainly associated with metabolism and immunity. Pathway analysis showed that immune-related pathways of phagosome and cell adhesion molecules (CAMs) pathway were significantly down-regulated under low temperature. Moreover, ferroptosis, a significantly changed pathway involved in tissue damage and acute renal failure, is reported here for the first time. The levels of serum parameters associated with kidney damage such as urea and uric acid (UA) increased significantly under low temperature. The immunofluorescence staining of the kidney showed that cell apoptosis occurred at low temperature. The results of the present study indicate that exposure to low temperature can cause kidney disfunction and down-regulate the immune-related pathway in the kidney of tilapia. This study provides new insight into the mechanism of kidney damage in fish under low temperature.


Asunto(s)
Cíclidos/fisiología , Frío/efectos adversos , Riñón/metabolismo , Transcriptoma , Animales , Cíclidos/genética , Análisis de Secuencia de ARN/veterinaria , Estrés Fisiológico
2.
Nucleic Acids Res ; 43(19): 9198-213, 2015 Oct 30.
Artículo en Inglés | MEDLINE | ID: mdl-26227973

RESUMEN

The transcriptional programs of ectothermic teleosts are directly influenced by water temperature. However, the cis- and trans-factors governing cold responses are not well characterized. We profiled transcriptional changes in eight zebrafish tissues exposed to mildly and severely cold temperatures using RNA-Seq. A total of 1943 differentially expressed genes (DEGs) were identified, from which 34 clusters representing distinct tissue and temperature response expression patterns were derived using the k-means fuzzy clustering algorithm. The promoter regions of the clustered DEGs that demonstrated strong co-regulation were analysed for enriched cis-regulatory elements with a motif discovery program, DREME. Seventeen motifs, ten known and seven novel, were identified, which covered 23% of the DEGs. Two motifs predicted to be the binding sites for the transcription factors Bcl6 and Jun, respectively, were chosen for experimental verification, and they demonstrated the expected cold-induced and cold-repressed patterns of gene regulation. Protein interaction modeling of the network components followed by experimental validation suggested that Jun physically interacts with Bcl6 and might be a hub factor that orchestrates the cold response in zebrafish. Thus, the methodology used and the regulatory networks uncovered in this study provide a foundation for exploring the mechanisms of cold adaptation in teleosts.


Asunto(s)
Respuesta al Choque por Frío/genética , Regulación de la Expresión Génica , Redes Reguladoras de Genes , Regiones Promotoras Genéticas , Pez Cebra/genética , Animales , Línea Celular , Femenino , Perfilación de la Expresión Génica , Ontología de Genes , Masculino , Motivos de Nucleótidos , Especificidad de Órganos , Mapeo de Interacción de Proteínas , Factores de Transcripción/metabolismo
3.
Zool Res ; 44(1): 126-141, 2023 Jan 18.
Artículo en Inglés | MEDLINE | ID: mdl-36419379

RESUMEN

Temperature tolerance restricts the distribution of a species. However, the molecular and cellular mechanisms that set the thermal tolerance limits of an organism are poorly understood. Here, we report on the function of dual-specificity phosphatase 1 (DUSP1) in thermal tolerance regulation. Notably, we found that dusp1 -/- zebrafish grew normally but survived within a narrowed temperature range. The higher susceptibility of these mutant fish to both cold and heat challenges was attributed to accelerated cell death caused by aggravated mitochondrial dysfunction and over-production of reactive oxygen species in the gills. The DUSP1-MAPK-DRP1 axis was identified as a key pathway regulating these processes in both fish and human cells. These observations suggest that DUSP1 may play a role in maintaining mitochondrial integrity and redox homeostasis. We therefore propose that maintenance of cellular redox homeostasis may be a key mechanism for coping with cellular thermal stress and that the interplay between signaling pathways regulating redox homeostasis in the most thermosensitive tissue (i.e., gills) may play an important role in setting the thermal tolerance limit of zebrafish.


Asunto(s)
Mitocondrias , Pez Cebra , Animales , Humanos , Pez Cebra/genética , Branquias , Especies Reactivas de Oxígeno , Homeostasis , Fosfatasa 1 de Especificidad Dual/genética
4.
J Mol Graph Model ; 91: 140-147, 2019 09.
Artículo en Inglés | MEDLINE | ID: mdl-31229805

RESUMEN

In present study, the NO oxidation on Ni-carbon nanocage and Ni-boron nitride nanocage surfaces was investigated. The Ni-C60 and Ni-B30N30 catalysts can oxidize the NO molecule by Langmuir-Hinshelwood (LH) and Eley-Rideal (ER) mechanisms. In this study, the NO molecule was joined to Ni atom of the Ni-surface-O2* and Ni-surface-O* to generate the intermediates with low barrier energies. It can be concluded that the cis-Ni-surface-ONOO* complex in the ER pathway is more stable than four-elements-ring complex in LH pathway ca 0.06 and 0.08 eV, respectively. In the LH pathway, the studied catalysts were deactivated by irreversible absorption of NO2 molecules in Ni atoms of Ni-C60 and Ni-B30N30. In contrast, in the ER pathway two NO2 molecules were released in the normal temperature. In this study, the abilities of the Ni-C60 and Ni-B30N30 to oxidation of NO molecule was demonstrated. Finally, the systematic scheme to design of metal-doped nano-catalysts to oxidation of toxic gases was proposed.


Asunto(s)
Compuestos de Boro/química , Fulerenos/química , Modelos Moleculares , Níquel/química , Óxido Nítrico/química , Adsorción , Oxidación-Reducción , Termodinámica
5.
Sci Rep ; 6: 28952, 2016 06 30.
Artículo en Inglés | MEDLINE | ID: mdl-27356472

RESUMEN

Transcriptional plasticity is a major driver of phenotypic differences between species. The lower temperature limit (LTL), namely the lower end of survival temperature, is an important trait delimiting the geographical distribution of a species, however, the genetic mechanisms are poorly understood. We investigated the inter-species transcriptional diversification in cold responses between zebrafish Danio rerio and tilapia Oreochromis niloticus, which were reared at a common temperature (28 °C) but have distinct LTLs. We identified significant expressional divergence between the two species in the orthologous genes from gills when the temperature cooled to the LTL of tilapia (8 °C). Five KEGG pathways were found sequentially over-represented in the zebrafish/tilapia divergently expressed genes in the duration (12 hour) of 8 °C exposure, forming a signaling cascade from metabolic regulation to apoptosis via FoxO signaling. Consistently, we found differential progression of apoptosis in the gills of the two species in which zebrafish manifested a delayed and milder apoptotic phenotype than tilapia, corresponding with a lower LTL of zebrafish. We identified diverged expression in 25 apoptosis-related transcription factors between the two species which forms an interacting network with diverged factors involving the FoxO signaling and metabolic regulation. We propose a genetic network which regulates LTL in fishes.


Asunto(s)
Frío , Redes Reguladoras de Genes , Estrés Fisiológico , Animales , Apoptosis , Perfilación de la Expresión Génica , Redes y Vías Metabólicas/genética , Tilapia/genética , Tilapia/fisiología , Pez Cebra/genética , Pez Cebra/fisiología
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