首页> 外文期刊>Journal of the Entomological Society of Ontario >ALTERNATIVE mRNA SPLICE VARIANTS IN DROSOPHILA DL2 CELLS FOLLOWING FLOCK HOUSE VIRUS INFECTION
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ALTERNATIVE mRNA SPLICE VARIANTS IN DROSOPHILA DL2 CELLS FOLLOWING FLOCK HOUSE VIRUS INFECTION

机译:鸡群病毒感染后果蝇DL2细胞的替代mRNA片段变体

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There is a paucity of information regarding the responses of the insect immune system to viral infection. In other metazoan cells and tissues mRNA splicing variants are frequently associated with viral infection. Here we analyzed transcripts of theDNA repair gene 8-oxoguanine DNA glycosylase generated prior to, and post, infection of Drosophila melanogaster macrophage-like DL-2 cells by Flock House Virus (FHV). In mock-infected controls we observed that 2% of the transcripts were incompletely processed, maintaining some but not all introns. Eight hours post-FHV infection of the DL-2 cells, we observed a seven fold increase in the frequency of immature Ogg1 transcripts. Moreover, there was a change in the introns retained in the transcripts observed compared with mock-infected controls, including completely unspliced transcripts. Surprisingly, the frequency of immature transcripts was reduced to control levels by 12 hours post-inoculation and remained relatively low tip to 48 hrs. These results support the conclusion that viral infection may be accompanied by a host-mediated partial inhibition of mRNA splicing factors. This phenomenon has the potential to generate novel splice variants that are neither directly useful to the host nor the infecting virus but have the potential to degrade the transmission of genetic information. To our knowledge this the first report that viral infection may Published November 2008
机译:关于昆虫免疫系统对病毒感染的反应的信息很少。在其他后生细胞和组织中,mRNA剪接变体经常与病毒感染相关。在这里,我们分析了果蝇房室病毒(FHV)感染果蝇黑巨噬细胞样DL-2细胞之前和之后产生的DNA修复基因8-氧鸟嘌呤DNA糖基化酶的转录本。在模拟感染的对照中,我们观察到2%的转录本未完全加工,保留了部分而非全部内含子。 FHV感染DL-2细胞后八小时,我们观察到未成熟Ogg1转录本的频率增加了七倍。此外,与模拟感染的对照(包括完全未剪接的转录本)相比,观察到的转录本中保留的内含子有所变化。出人意料的是,未成熟转录本的频率在接种后12小时降低到了对照水平,并保持相对较低的尖端至48小时。这些结果支持病毒感染可能伴随宿主介导的对mRNA剪接因子的部分抑制的结论。这种现象有可能产生新的剪接变体,这些变体既不能直接用于宿主也不能直接用于感染病毒,但有可能降低遗传信息的传递。据我们所知,这是第一份有关病毒感染的报告,2008年11月发布

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