Analysis of NS2-dependent effects on influenza PB1 segment extends replication requirements beyond the canonical promoter
Abstract
Abstract Influenza A virus encodes conserved promoter sequences. Using minimal replication assays—transfections with viral polymerase, nucleoprotein, and a genomic template—these sequences were identified as 13nt at the 5’ end of the genomic RNA (U13) and 12nt at the 3’ end (U12). Other than the fourth 3’ nucleotide, the U12 and U13 sequences are identical between all eight RNA molecules of the segmented influenza A genome. However, individual segments can exhibit different dynamics during infection. Influenza NS2, which modulates transcription and replication differentially between genomic segments, may provide an explanation. Here, we assess how internal sequences of two genomic segments, HA and PB1, contribute to NS2-dependent replication and map such interactions down to individual nucleotides in PB1. We find that the expression of NS2 significantly alters sequence requirements for efficient replication beyond the identical U12 and U13 sequences, providing a potential mechanism for segment-specific replication dynamics across the influenza genome.
Article Details
Authors (8)
Sharmada Swaminath
Department of Molecular Biology, School of Biological Sciences, University of California
Marisa Mendes
Department of Molecular Biology, School of Biological Sciences, University of California
Yipeng Zhang
State Key Laboratory of Crop Genetics and Germplasm Enhancement and Utilization, Zhongshan Biological Breeding Laboratory, Jiangsu Nanjing Rice Germplasm Resources National Field Observation and Research Station, Nanjing Agricultural University
Kaleigh A. Remick
Isabel Mejia
Melissa Güereca
Aartjan J. W. te Velthuis
Alistair B. Russell
Department of Molecular Biology, School of Biological Sciences, University of California