Key result
During poliovirus RNA replication, poly(A) and VPg-linked poly(U) sequences act as reciprocal templates, producing homopolymeric products that are frequently longer than their respective templates.
The study elucidates a reiterative transcription mechanism in poliovirus RNA replication that ensures the synthesis of long 3' poly(A) tails.
Reveals reiterative transcription for long poly(A) tails in poliovirus; leaves open conservation across picornaviruses and antiviral implications.
A 3' poly(A) tail is a common feature of picornavirus RNA genomes and the RNA genomes of many other positive-strand RNA viruses. We examined the manner in which the homopolymeric poly(A) and poly(U) portions of poliovirus (PV) positive- and negative-strand RNAs were used as reciprocal templates during RNA replication. Poly(A) sequences at the 3' end of viral positive-strand RNA were transcribed into VPg-linked poly(U) products at the 5' end of negative-strand RNA during PV RNA replication. Subsequently, VPg-linked poly(U) sequences at the 5' ends of negative-strand RNA templates were transcribed into poly(A) sequences at the 3' ends of positive-strand RNAs. The homopolymeric poly(A) and poly(U) portions of PV RNA products of replication were heterogeneous in length and frequently longer than the corresponding homopolymeric sequences of the respective viral RNA templates. The data support a model of PV RNA replication wherein reiterative transcription of homopolymeric templates ensures the synthesis of long 3' poly(A) tails on progeny RNA genomes.
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Steil et al. (2010) studied Poliovirus RNA replication. Poliovirus RNA templates with defined poly(A) sequences was evaluated on Length of VPg-linked poly(U) products and poly(A) tails. During poliovirus RNA replication, poly(A) and VPg-linked poly(U) sequences act as reciprocal templates, producing homopolymeric products that are frequently longer than their respective templates.
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