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Genetic elements regulating packaging of the Bunyamwera orthobunyavirus genome.
Kohl, Alain; Lowen, Anice C; Léonard, Vincent H J; Elliott, Richard M.
Affiliation
  • Kohl A; Division of Virology, Institute of Biomedical and Life Sciences, University of Glasgow, Glasgow G11 5JR, Scotland, UK.
  • Lowen AC; Division of Virology, Institute of Biomedical and Life Sciences, University of Glasgow, Glasgow G11 5JR, Scotland, UK.
  • Léonard VHJ; Division of Virology, Institute of Biomedical and Life Sciences, University of Glasgow, Glasgow G11 5JR, Scotland, UK.
  • Elliott RM; Division of Virology, Institute of Biomedical and Life Sciences, University of Glasgow, Glasgow G11 5JR, Scotland, UK.
J Gen Virol ; 87(Pt 1): 177-187, 2006 Jan.
Article in En | MEDLINE | ID: mdl-16361430
The genome of Bunyamwera virus (BUN; family Bunyaviridae, genus Orthobunyavirus) comprises three segments of negative-sense, single-stranded RNA. The RNA segments are encapsidated by the viral nucleocapsid (N) protein and form panhandle-like structures through interaction of complementary sequences at their 5' and 3' termini. Transcription and replication of a BUN genome analogue (minireplicon), comprising the viral non-coding sequences flanking a reporter gene, requires just the viral RNA polymerase (L protein) and N protein. Here, sequences of Bunyamwera serogroup M segment RNAs were compared and conserved elements within nt 20-33 of the 3' and 5' non-coding regions that can affect packaging of minireplicons into virions were identified. RNA-folding models suggest that a conserved sequence within nt 20-33 of the 5' end of the genome segments maintains conserved structural features necessary for efficient transcription. Competitive packaging experiments using M, L and S segment-derived minireplicons that encode different reporter genes showed variable packaging efficiencies of the three segments. Packaging of a particular segment appeared to be independent of the presence of other segments and, for the S segment, packaging efficiency was unaffected by the inclusion of viral coding sequences in the minireplicon.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Viral Proteins / Virus Replication / Bunyamwera virus / Virus Assembly Type of study: Prognostic_studies Language: En Journal: J Gen Virol Year: 2006 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Viral Proteins / Virus Replication / Bunyamwera virus / Virus Assembly Type of study: Prognostic_studies Language: En Journal: J Gen Virol Year: 2006 Document type: Article Country of publication: United kingdom