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Multiplatform next-generation sequencing identifies novel RNA molecules and transcript isoforms of the endogenous retrovirus isolated from cultured cells

机译:多平台下一代测序可鉴定从培养细胞中分离出的内源性逆转录病毒的新型RNA分子和转录亚型

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摘要

In this study, we applied short- and long-read RNA sequencing techniques, as well as PCR analysis to investigate the transcriptome of the porcine endogenous retrovirus (PERV) expressed from cultured porcine kidney cell line PK-15. This analysis has revealed six novel transcripts and eight transcript isoforms, including five length and three splice variants. We were able to establish whether a deletion in a transcript is the result of the splicing of mRNAs or of genomic deletion in one of the PERV clones. Additionally, we re-annotated the formerly identified RNA molecules. Our analysis revealed a higher complexity of PERV transcriptome than it was earlier believed.
机译:在这项研究中,我们应用了短读和长读RNA测序技术,以及PCR分析来研究从培养的猪肾细胞系PK-15表达的猪内源性逆转录病毒(PERV)的转录组。该分析揭示了六个新颖的转录本和八个转录本的同工型,包括五个长度和三个剪接变体。我们能够确定转录本中的缺失是否是其中一个PERV克隆中的mRNA剪接或基因组缺失的结果。此外,我们重新注释了以前确定的RNA分子。我们的分析显示,PERV转录组的复杂性比以前认为的要高。

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