A 5′ RNA element promotes dengue virus RNA synthesis on a circular genome

  1. Claudia V. Filomatori1,
  2. Maria F. Lodeiro1,
  3. Diego E. Alvarez1,
  4. Marcelo M. Samsa1,
  5. Lía Pietrasanta2,3, and
  6. Andrea V. Gamarnik1,3,4
  1. 1Fundación Instituto Leloir, Buenos Aires C1405BWE, Argentina;
  2. 2Centro de Microscopías Avanzadas, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires C1428BEHA, Argentina;
  3. 3Consejo Nacional de Investigaciones Científicas y Tecnológicas de Argentina, Buenos Aires C1033AAJ, Argentina

    Abstract

    The mechanisms of RNA replication of plus-strand RNA viruses are still unclear. Here, we identified the first promoter element for RNA synthesis described in a flavivirus. Using dengue virus as a model, we found that the viral RdRp discriminates the viral RNA by specific recognition of a 5′ element named SLA. We demonstrated that RNA–RNA interactions between 5′ and 3′ end sequences of the viral genome enhance dengue virus RNA synthesis only in the presence of an intact SLA. We propose a novel mechanism for minus-strand RNA synthesis in which the viral polymerase binds SLA at the 5′ end of the genome and reaches the site of initiation at the 3′ end via long-range RNA–RNA interactions. These findings provide an explanation for the strict requirement of dengue virus genome cyclization during viral replication.

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