Nucleocapsids of the Rift Valley fever virus ambisense S segment contain an exposed RNA element in the center that overlaps with the intergenic region

Rift Valley fever virus (RVFV) is a mosquito-borne zoonotic pathogen. Its RNA genome consists of two negative-sense segments (L and M) with one gene each, and one ambisense segment (S) with two opposing genes separated by the noncoding "intergenic region" (IGR). These vRNAs and the complementary cRNAs are encapsidated by nucleoprotein (N). Using iCLIP2 (individual-nucleotide resolution UV crosslinking and immunoprecipitation) to map all N-vRNA and N-cRNA interactions, we detect N coverage along the L and M segments. However, the S segment vRNA and cRNA each contain approximately 100 non-encapsidated nucleotides stretching from the IGR into the 5'-adjacent reading frame. These exposed regions are RNase-sensitive and predicted to form stem-loop structures with the mRNA transcription termination motif positioned near the top. Moreover, optimal S segment transcription and replication requires the entire exposed region rather than only the IGR. Thus, the RVFV S segment contains a central, non-encapsidated RNA region with a functional role.

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Publication Details

Journal
Nature Communications
Published
2024-09-01
DOI
https://doi.org/10.1038/s41467-024-52058-2
Citations
4
Primary Topic
Viral Infections and Vectors
Type
article
Field-Weighted Citation Impact
1.56

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article

Nucleocapsids of the Rift Valley fever virus ambisense S segment contain an exposed RNA element in the center that overlaps with the intergenic region

Torsten Hain, Patrick Barth, Lyudmila Shalamova, Katharina Humpert et al.
4 citations
Nature Communications
Viral Infections and Vectors
1.56
article

Nucleocapsids of the Rift Valley fever virus ambisense S segment contain an exposed RNA element in the center that overlaps with the intergenic region

Torsten Hain, Patrick Barth, Lyudmila Shalamova, Katharina Humpert, Oliver Roßbach, Alejandro Brun, Gema Lorenzo, Matthew J. Pickin, Stefan Janssen, Roland K. Hartmann, Alexander Goesmann, Friedemann Weber, Kiriaki Kouti, Benjamin Ott
article en
4 citations

Abstract

Rift Valley fever virus (RVFV) is a mosquito-borne zoonotic pathogen. Its RNA genome consists of two negative-sense segments (L and M) with one gene each, and one ambisense segment (S) with two opposing genes separated by the noncoding "intergenic region" (IGR). These vRNAs and the complementary cRNAs are encapsidated by nucleoprotein (N). Using iCLIP2 (individual-nucleotide resolution UV crosslinking and immunoprecipitation) to map all N-vRNA and N-cRNA interactions, we detect N coverage along the L and M segments. However, the S segment vRNA and cRNA each contain approximately 100 non-encapsidated nucleotides stretching from the IGR into the 5'-adjacent reading frame. These exposed regions are RNase-sensitive and predicted to form stem-loop structures with the mRNA transcription termination motif positioned near the top. Moreover, optimal S segment transcription and replication requires the entire exposed region rather than only the IGR. Thus, the RVFV S segment contains a central, non-encapsidated RNA region with a functional role.

Nature CommunicationsVol. 15(1)
Philipps University of Marburg (DE), Justus-Liebig-Universität Gießen (DE), Centro de Investigación en Sanidad Animal, University of Regensburg (DE)
European Commission, Deutsche Forschungsgemeinschaft, Vetenskapsrådet, Ministerio de Ciencia e Innovación, European Regional Development Fund, Agencia Estatal de Investigación
Openalex Percentile: Top 17%
Viral Infections and Vectors
1.56
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