Unraveling the hidden diversity of endogenous bornavirus-like elements derived from ancient orthobornaviral X and P genes in mammalian genomes

Endogenous bornavirus-like elements (EBLs) are heritable sequences derived from bornaviruses in vertebrate genomes, which are strongly suggested to originate from transcripts of ancient bornaviruses. EBLs have been detected by sequence similarity searches, such as tBLASTn, and thus EBLs derived from...

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Bibliographic Details
Published inbioRxiv
Main Authors Bea Clarise Baluyot Garcia, Mukai, Yahiro, Tomonaga, Keizo, Horie, Masayuki
Format Paper
LanguageEnglish
Published Cold Spring Harbor Cold Spring Harbor Laboratory Press 06.05.2022
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Summary:Endogenous bornavirus-like elements (EBLs) are heritable sequences derived from bornaviruses in vertebrate genomes, which are strongly suggested to originate from transcripts of ancient bornaviruses. EBLs have been detected by sequence similarity searches, such as tBLASTn, and thus EBLs derived from small and/or rapidly evolving viral genes, such as viral X and P genes, are difficult to be detected. Indeed, no EBLs derived from X and P genes of orthobornaviruses were detected. Thus, although previous studies comprehensively analyzed the presence of EBLs in vertebrate genomes, there may still be undetectable EBLs. In this study, we developed a novel strategy to detect such "hidden" EBLs by focusing on the nature of readthrough transcription of orthobornavirus. We showed a series of evidence supporting that there are EBLs derived from orthobornaviral X and P genes in mammalian genomes. Therefore, this study contributes to a deeper understanding of the evolution of ancient viruses and of virus-host relationships. Further, our data also suggest that endogenous viral elements detected thus far are just the tip of the iceberg, and thus further studies are required to understand ancient viruses more accurately. Competing Interest Statement The authors have declared no competing interest.
Bibliography:content type line 50
SourceType-Working Papers-1
ObjectType-Working Paper/Pre-Print-1
ISSN:2692-8205
2692-8205
DOI:10.1101/2022.05.06.490909