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Deep RNA Sequencing Reveals Hidden Features and Dynamics of Early Gene Transcription in Paramecium bursaria Chlorella Virus 1

机译:深度RNA测序揭示了草履虫法球菌小球藻病毒1的隐藏特征和早期基因转录的动力学。

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摘要

Paramecium bursaria chlorella virus 1 (PBCV-1) is the prototype of the genus Chlorovirus (family Phycodnaviridae) that infects the unicellular, eukaryotic green alga Chlorella variabilis NC64A. The 331-kb PBCV-1 genome contains 416 major open reading frames. A mRNA-seq approach was used to analyze PBCV-1 transcriptomes at 6 progressive times during the first hour of infection. The alignment of 17 million reads to the PBCV-1 genome allowed the construction of single-base transcriptome maps. Significant transcription was detected for a subset of 50 viral genes as soon as 7 min after infection. By 20 min post infection (p.i.), transcripts were detected for most PBCV-1 genes and transcript levels continued to increase globally up to 60 min p.i., at which time 41% or the poly (A+)-containing RNAs in the infected cells mapped to the PBCV-1 genome. For some viral genes, the number of transcripts in the latter time points (20 to 60 min p.i.) was much higher than that of the most highly expressed host genes. RNA-seq data revealed putative polyadenylation signal sequences in PBCV-1 genes that were identical to the polyadenylation signal AAUAAA of green algae. Several transcripts have an RNA fragment excised. However, the frequency of excision and the resulting putative shortened protein products suggest that most of these excision events have no functional role but are probably the result of the activity of misled splicesomes.
机译:草履虫法氏小球藻小病毒1(PBCV-1)是感染单细胞,真核绿藻小球藻NC64A的绿病毒属(Phycodnaviridae)的原型。 331kb PBCV-1基因组包含416个主要的开放阅读框。在感染的第一小时内,mRNA-seq方法用于在6个进行时间分析PBCV-1转录组。对PBCV-1基因组进行的1,700万次读取的比对允许构建单碱基转录组图谱。感染后7分钟,就检测到50个病毒基因的子集的重要转录。感染后(pi)20分钟,检测到大多数PBCV-1基因的转录本,直到pi 60分钟为止,转录本水平总体上持续增加,此时受感染细胞中有41%或含多聚(A +)的RNAs被定位PBCV-1基因组。对于某些病毒基因,在后一个时间点(20至60分钟p.i.)的转录物数量要比表达最高的宿主基因的转录物数量高得多。 RNA-seq数据显示PBCV-1基因中假定的聚腺苷酸化信号序列与绿藻的聚腺苷酸化信号AAUAAA相同。几个转录本有一个RNA片段被切除。但是,切除的频率和由此推定的缩短的蛋白质产物表明,大多数这些切除事件没有功能性作用,但可能是错配剪接体活性的结果。

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