首页> 美国卫生研究院文献>American Journal of Physiology - Cell Physiology >Cell-to-Cell Communication and Signaling Pathways: miR-958 inhibits Toll signaling and Drosomycin expression via direct targeting of Toll and Dif in Drosophila melanogaster
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Cell-to-Cell Communication and Signaling Pathways: miR-958 inhibits Toll signaling and Drosomycin expression via direct targeting of Toll and Dif in Drosophila melanogaster

机译:细胞间通信和信号传导途径:miR-958通过直接靶向果蝇中的Toll和Dif抑制Toll信号传导和果蝇表达。

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摘要

Drosophila melanogaster is widely used as a model system to study innate immunity and signaling pathways related to innate immunity, including the Toll signaling pathway. Although this pathway is well studied, the precise mechanisms of posttranscriptional regulation of key components of the Toll signaling pathway by microRNAs (miRNAs) remain obscure. In this study, we used an in silico strategy in combination with the Gal80ts-Gal4 driver system to identify microRNA-958 (miR-958) as a candidate Toll pathway regulating miRNA in Drosophila. We report that overexpression of miR-958 significantly reduces the expression of Drosomycin, a key antimicrobial peptide involved in Toll signaling and the innate immune response. We further demonstrate in vitro and in vivo that miR-958 targets the Toll and Dif genes, key components of the Toll signaling pathway, to negatively regulate Drosomycin expression. In addition, a miR-958 sponge rescued the expression of Toll and Dif, resulting in increased expression of Drosomycin. These results, not only revealed a novel function and modulation pattern of miR-958, but also provided a new insight into the underlying molecular mechanisms of Toll signaling in regulation of innate immunity.
机译:果蝇(Drosophila melanogaster)被广泛用作研究先天免疫和与先天免疫相关的信号通路,包括Toll信号通​​路的模型系统。尽管对此途径进行了充分研究,但通过microRNA(miRNA)对Toll信号传导途径的关键成分进行转录后调控的精确机制仍然不清楚。在这项研究中,我们将计算机策略与Gal80 ts -Gal4驱动程序系统结合使用,以确定microRNA-958(miR-958)作为果蝇中调控miRNA的候选Toll途径。我们报道,miR-958的过表达显着降低了果糖霉素的表达,果糖霉素是参与Toll信号传导和先天免疫应答的关键抗菌肽。我们进一步在体外和体内证明了miR-958靶向Toll和Dif基因(Toll信号传导途径的关键组成部分)来负调控果蝇霉素的表达。此外,miR-958海绵可以挽救Toll和Dif的表达,从而提高果蝇霉素的表达。这些结果不仅揭示了miR-958的新颖功能和调节模式,而且还提供了对Toll信号传导调控先天免疫的潜在分子机制的新见解。

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