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Structural and functional conservation of cis-acting RNA elements in coronavirus 5'-terminal genome regions.
Madhugiri, Ramakanth; Karl, Nadja; Petersen, Daniel; Lamkiewicz, Kevin; Fricke, Markus; Wend, Ulrike; Scheuer, Robina; Marz, Manja; Ziebuhr, John.
Affiliation
  • Madhugiri R; Institute of Medical Virology, Justus Liebig University, Giessen, Germany.
  • Karl N; Institute of Medical Virology, Justus Liebig University, Giessen, Germany.
  • Petersen D; Institute of Medical Virology, Justus Liebig University, Giessen, Germany.
  • Lamkiewicz K; Faculty of Mathematics and Computer Science, Friedrich Schiller University, Jena, Germany; European Virus Bioinformatics Center, Jena, Germany.
  • Fricke M; Faculty of Mathematics and Computer Science, Friedrich Schiller University, Jena, Germany; European Virus Bioinformatics Center, Jena, Germany.
  • Wend U; Institute of Medical Virology, Justus Liebig University, Giessen, Germany.
  • Scheuer R; Institute of Medical Virology, Justus Liebig University, Giessen, Germany.
  • Marz M; Faculty of Mathematics and Computer Science, Friedrich Schiller University, Jena, Germany; FLI Leibniz Institute for Age Research, Jena, Germany; European Virus Bioinformatics Center, Jena, Germany.
  • Ziebuhr J; Institute of Medical Virology, Justus Liebig University, Giessen, Germany; European Virus Bioinformatics Center, Jena, Germany. Electronic address: john.ziebuhr@viro.med.uni-giessen.de.
Virology ; 517: 44-55, 2018 04.
Article in En | MEDLINE | ID: mdl-29223446
ABSTRACT
Structure predictions suggest a partial conservation of RNA structure elements in coronavirus terminal genome regions. Here, we determined the structures of stem-loops (SL) 1 and 2 of two alphacoronaviruses, human coronavirus (HCoV) 229E and NL63, by RNA structure probing and studied the functional relevance of these putative cis-acting elements. HCoV-229E SL1 and SL2 mutants generated by reverse genetics were used to study the effects on viral replication of single-nucleotide substitutions predicted to destabilize the SL1 and SL2 structures. The data provide conclusive evidence for the critical role of SL1 and SL2 in HCoV-229E replication and, in some cases, revealed parallels with previously characterized betacoronavirus SL1 and SL2 elements. Also, we were able to rescue viable HCoV-229E mutants carrying replacements of SL2 with equivalent betacoronavirus structural elements. The data obtained in this study reveal a remarkable degree of structural and functional conservation of 5'-terminal RNA structural elements across coronavirus genus boundaries.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Regulatory Sequences, Nucleic Acid / Genome, Viral / Coronavirus 229E, Human / Coronavirus NL63, Human Limits: Humans Language: En Journal: Virology Year: 2018 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Regulatory Sequences, Nucleic Acid / Genome, Viral / Coronavirus 229E, Human / Coronavirus NL63, Human Limits: Humans Language: En Journal: Virology Year: 2018 Document type: Article Affiliation country: