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Direct translation of incoming retroviral genomes

Viruses that carry a positive-sense, single-stranded (+ssRNA) RNA translate their genomes soon after entering the host cell to produce viral proteins, with the exception of retroviruses. A distinguishing feature of retroviruses is reverse transcription, where the +ssRNA genome serves as a template t...

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Hauptverfasser: Köppke, Julia (VerfasserIn) , Keller, Luise-Elektra (VerfasserIn) , Stuck, Michelle (VerfasserIn) , Arnow, Nicolas D. (VerfasserIn) , Bannert, Norbert (VerfasserIn) , Döllinger, Jörg (VerfasserIn) , Cingöz, Oya (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 05 January 2024
In: Nature Communications
Year: 2024, Jahrgang: 15, Pages: 1-12
ISSN:2041-1723
DOI:10.1038/s41467-023-44501-7
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.1038/s41467-023-44501-7
Verlag, kostenfrei, Volltext: https://www.nature.com/articles/s41467-023-44501-7
Volltext
Verfasserangaben:Julia Köppke, Luise-Elektra Keller, Michelle Stuck, Nicolas D. Arnow, Norbert Bannert, Joerg Doellinger & Oya Cingöz
Beschreibung
Zusammenfassung:Viruses that carry a positive-sense, single-stranded (+ssRNA) RNA translate their genomes soon after entering the host cell to produce viral proteins, with the exception of retroviruses. A distinguishing feature of retroviruses is reverse transcription, where the +ssRNA genome serves as a template to synthesize a double-stranded DNA copy that subsequently integrates into the host genome. As retroviral RNAs are produced by the host cell transcriptional machinery and are largely indistinguishable from cellular mRNAs, we investigated the potential of incoming retroviral genomes to directly express proteins. Here we show through multiple, complementary methods that retroviral genomes are translated after entry. Our findings challenge the notion that retroviruses require reverse transcription to produce viral proteins. Synthesis of retroviral proteins in the absence of productive infection has significant implications for basic retrovirology, immune responses and gene therapy applications.
Beschreibung:Gesehen am 11.03.2024
Beschreibung:Online Resource
ISSN:2041-1723
DOI:10.1038/s41467-023-44501-7

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