Mechanism for de novo initiation at two sites in the respiratory syncytial virus promoter

Abstract The respiratory syncytial virus (RSV) RNA dependent RNA polymerase (RdRp) initiates two RNA synthesis processes from the viral promoter: genome replication from position 1U and mRNA transcription from position 3C. Here, we examined the mechanism by which a single promoter can direct initiat...

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Bibliographic Details
Published in:Nucleic acids research 2018-07, Vol.46 (13), p.6785-6796
Main Authors: Cressey, Tessa N, Noton, Sarah L, Nagendra, Kartikeya, Braun, Molly R, Fearns, Rachel
Format: Article
Language:English
Subjects:
Nucleic Acid Enzymes
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Summary:Abstract The respiratory syncytial virus (RSV) RNA dependent RNA polymerase (RdRp) initiates two RNA synthesis processes from the viral promoter: genome replication from position 1U and mRNA transcription from position 3C. Here, we examined the mechanism by which a single promoter can direct initiation from two sites. We show that initiation at 1U and 3C occurred independently of each other, and that the same RdRp was capable of precisely selecting the two sites. The RdRp preferred to initiate at 3C, but initiation site selection could be modulated by the relative concentrations of ATP versus GTP. Analysis of template mutations indicated that the RdRp could bind ATP and CTP, or GTP, independently of template nucleotides. The data suggest a model in which innate affinity of the RdRp for particular NTPs, coupled with a repeating element within the promoter, allows precise initiation of replication at 1U or transcription at 3C.
ISSN:0305-1048
1362-4962
DOI:10.1093/nar/gky480