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受感染植物细胞中病毒颗粒和多核糖体内马铃薯A病毒RNA基因组的定位与定量分析。

Mapping and quantification of potato virus A RNA genomes within viral particles and polysomes in infected plant cells.

作者信息

Dutta Pinky, Mäkinen Kristiina

机构信息

Viikki Plants Science Centre and Department of Agricultural Sciences, Faculty of Agriculture and Forestry, University of Helsinki, Finland.

Viikki Plants Science Centre and Department of Agricultural Sciences, Faculty of Agriculture and Forestry, University of Helsinki, Finland.

出版信息

J Virol Methods. 2025 Feb;332:115066. doi: 10.1016/j.jviromet.2024.115066. Epub 2024 Nov 15.

Abstract

Potato virus A belongs to the genus Potyvirus, a group of single-stranded positive sense RNA viruses infecting crops worldwide. To initiate infection in a host, its genome takes part in different activities, viz., translation, replication, encapsidation during the infection cycle. Extensive research has been carried out to scrutinize the stages of potyviral infection cycle and decipher the strategies it employs to cause disease. Nonetheless, the amount of viral RNA taking part in translation and virion formation, at a given time point, is missing. In this study, we quantified the percentage of viral RNA that exists as virions and those that associates with host polysome, relative to total viral RNA in infected plant tissue. We employed a revised version of immuno-capture reverse transcription PCR and polysome profiling to address our queries. We tested three different coating antibody concentrations and further optimized the immuno-capture reverse transcription PCR protocol to address its limitation of binding and retaining viral particles. Our results indicate that most of the viral RNA (69 %) exists as encapsidated genomes, while 3 % of total viral RNA associates with host polysomes. These findings are crucial for correct interpretation of quantitative translational studies in which correlation must be made between the number of polysome-associated transcripts and the amount of protein synthesized.

摘要

马铃薯A病毒属于马铃薯Y病毒属,是一类感染全球农作物的单链正义RNA病毒。为了在宿主中引发感染,其基因组在感染周期中参与不同的活动,即翻译、复制、衣壳化。人们已经进行了广泛的研究来仔细检查马铃薯Y病毒感染周期的各个阶段,并破译其致病策略。然而,在给定时间点参与翻译和病毒粒子形成的病毒RNA的量尚不清楚。在本研究中,我们相对于受感染植物组织中的总病毒RNA,定量了以病毒粒子形式存在的病毒RNA以及与宿主多核糖体相关的病毒RNA的百分比。我们采用了免疫捕获逆转录PCR的修订版和多核糖体分析来解决我们的问题。我们测试了三种不同的包被抗体浓度,并进一步优化了免疫捕获逆转录PCR方案,以解决其结合和保留病毒颗粒的局限性的局限性。我们的结果表明,大多数病毒RNA(69%)以衣壳化基因组的形式存在,而总病毒RNA的3%与宿主多核糖体相关。这些发现对于正确解释定量翻译研究至关重要,在定量翻译研究中,必须在多核糖体相关转录本的数量与合成的蛋白质量之间建立相关性。

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