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- W2887133119 abstract "The recognition of microbial pathogens, which is mediated by pattern recognition receptors (PRRs), is critical to the initiation of innate immune responses. In the present study, we isolated the full-length cDNA and genomic DNA sequences of the MDA5, LGP2 and MAVS genes in Nile tilapia, termed OnMDA5, OnLGP2 and OnMAVS. The OnMDA5 gene encodes 974 amino acids and contains two caspase-associated recruitment domains (CARDs), a DExDc domain (DExD/H box-containing domain), a HELICc (helicase superfamily C-terminal) domain and a C-terminal regulatory domain (RD). The OnLGP2 gene encodes 679 amino acids and contains a DExDc, a HELICc and an RD. The OnMAVS gene encodes 556 amino acids and contains a CARD, a proline-rich domain, a transmembrane helix domain and a putative TRAF2-binding motif (269PVQDT273). Phylogenetic analyses showed that all three genes from Nile tilapia were clustered together with their counterparts from other teleost fishes. Real-time PCR analyses showed that all three genes were constitutively expressed in all examined tissues in Nile tilapia. OnMDA5 presented the highest expression level in the blood and the lowest expression level in the liver, while OnMAVS presented the highest expression level in the kidney. The highest expression level of OnLGP2 was detected in the liver. An examination of the expression patterns of these RIG-I-like receptors (RLRs) during embryonic development showed that the highest expression levels of OnMDA5 occurred at 2 days postfertilization (dpf), and the expression significantly decreased from 3 to 8 dpf. The expression levels of OnLGP2 significantly increased from 4 to 8 dpf. The expression levels of OnMAVS mRNA were stable from 2 to 8 dpf. Upon stimulation by intraperitoneal injection of Streptococcus agalactiae, the expression levels of OnMDA5 were first downregulated and then upregulated in the blood, gill and spleen. In the intestine and kidney, the expression of OnMDA5 was first upregulated, then downregulated, and then upregulated again. The expression of OnLGP2 was upregulated in the kidney and intestine, and the expression of OnMAVS was upregulated in the spleen. Overexpression of OnMAVS increased NF-κB activation in 293 T cells (p < 0.05), and after cotransfection with OnMDA5, the OnMAVS-dependent NF-κB activation was slightly increased (p > 0.05), after cotransfection with OnLGP2, the OnMAVS-dependent NF-κB activation was significantly decreased (p < 0.05). These findings suggest that, although the deduced protein structure of OnMDA5 is evolutionarily conserved with the structures of other RLR members, its signal transduction function is markedly different. The results also suggest that OnLGP2 has a negative regulatory effect on the OnMAVS gene. OnMDA5 and OnMAVS were uniformly distributed throughout the cytoplasm in 293 T cells, whereas OnLGP2 was distributed throughout the cytoplasm and nucleus. These results are helpful for clarifying the innate immune response against bacterial infection in Nile tilapia." @default.
- W2887133119 created "2018-08-22" @default.
- W2887133119 creator A5008312038 @default.
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- W2887133119 date "2018-11-01" @default.
- W2887133119 modified "2023-10-18" @default.
- W2887133119 title "Molecular characterization and function analysis of three RIG-I-like receptor signaling pathway genes (MDA5, LGP2 and MAVS) in Oreochromis niloticus" @default.
- W2887133119 cites W1049059345 @default.
- W2887133119 cites W1847842222 @default.
- W2887133119 cites W1966759986 @default.
- W2887133119 cites W1968909382 @default.
- W2887133119 cites W1969601023 @default.
- W2887133119 cites W1977922844 @default.
- W2887133119 cites W1982570980 @default.
- W2887133119 cites W1990061756 @default.
- W2887133119 cites W1990619882 @default.
- W2887133119 cites W1993063850 @default.
- W2887133119 cites W1994527775 @default.
- W2887133119 cites W1995744610 @default.
- W2887133119 cites W2004312418 @default.
- W2887133119 cites W2006906174 @default.
- W2887133119 cites W2006906526 @default.
- W2887133119 cites W2008116827 @default.
- W2887133119 cites W2013433092 @default.
- W2887133119 cites W2014414190 @default.
- W2887133119 cites W2015623842 @default.
- W2887133119 cites W2016401408 @default.
- W2887133119 cites W2018828712 @default.
- W2887133119 cites W2019234632 @default.
- W2887133119 cites W2021128910 @default.
- W2887133119 cites W2025596585 @default.
- W2887133119 cites W2027388123 @default.
- W2887133119 cites W2031388429 @default.
- W2887133119 cites W2032558535 @default.
- W2887133119 cites W2032948492 @default.
- W2887133119 cites W2032980461 @default.
- W2887133119 cites W2037502650 @default.
- W2887133119 cites W2038992497 @default.
- W2887133119 cites W2040813747 @default.
- W2887133119 cites W2046523051 @default.
- W2887133119 cites W2049309853 @default.
- W2887133119 cites W2050607396 @default.
- W2887133119 cites W2055774592 @default.
- W2887133119 cites W2062490839 @default.
- W2887133119 cites W2063641548 @default.
- W2887133119 cites W2066425910 @default.
- W2887133119 cites W2066728093 @default.
- W2887133119 cites W2076063129 @default.
- W2887133119 cites W2078575853 @default.
- W2887133119 cites W2080208080 @default.
- W2887133119 cites W2087804239 @default.
- W2887133119 cites W2087888580 @default.
- W2887133119 cites W2089510415 @default.
- W2887133119 cites W2093579074 @default.
- W2887133119 cites W2093755635 @default.
- W2887133119 cites W2095401221 @default.
- W2887133119 cites W2100665873 @default.
- W2887133119 cites W2107513655 @default.
- W2887133119 cites W2119492463 @default.
- W2887133119 cites W2125566625 @default.
- W2887133119 cites W2132632499 @default.
- W2887133119 cites W2133449490 @default.
- W2887133119 cites W2136329789 @default.
- W2887133119 cites W2137303998 @default.
- W2887133119 cites W2137518728 @default.
- W2887133119 cites W2138560966 @default.
- W2887133119 cites W2140821779 @default.
- W2887133119 cites W2141137217 @default.
- W2887133119 cites W2148811254 @default.
- W2887133119 cites W2151713498 @default.
- W2887133119 cites W2154775599 @default.
- W2887133119 cites W2155290641 @default.
- W2887133119 cites W2316631363 @default.
- W2887133119 cites W2316712183 @default.
- W2887133119 cites W2398737414 @default.
- W2887133119 cites W2418728439 @default.
- W2887133119 cites W2474224431 @default.
- W2887133119 cites W2475068950 @default.
- W2887133119 cites W2478247020 @default.
- W2887133119 cites W2509321710 @default.
- W2887133119 cites W2514095198 @default.
- W2887133119 cites W2518953417 @default.
- W2887133119 cites W2572113976 @default.
- W2887133119 cites W2615529089 @default.
- W2887133119 cites W2754154512 @default.
- W2887133119 cites W837892414 @default.
- W2887133119 doi "https://doi.org/10.1016/j.fsi.2018.08.008" @default.
- W2887133119 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30099139" @default.
- W2887133119 hasPublicationYear "2018" @default.
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