pp32 and APRIL are host cell-derived regulators of influenza virus RNA synthesis from cRNA.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 26512887.
- Also identified by DOI 10.7554/eLife.08939 and PMC identifier 4718810.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Replication of influenza viral genomic RNA (vRNA) is catalyzed by viral RNA-dependent RNA polymerase (vRdRP). Complementary RNA (cRNA) is first copied from vRNA, and progeny vRNAs are then amplified from the cRNA. Although vRdRP and viral RNA are minimal requirements, efficient cell-free replication could not be reproduced using only these viral factors. Using a biochemical complementation assay system, we found a novel activity in the nuclear extracts of uninfected cells, designated IREF-2, that allows robust unprimed vRNA synthesis from a cRNA template. IREF-2 was shown to consist of host-derived proteins, pp32 and APRIL. IREF-2 interacts with a free form of vRdRP and preferentially upregulates vRNA synthesis rather than cRNA synthesis. Knockdown experiments indicated that IREF-2 is involved in in vivo viral replication. On the basis of these results and those of previous studies, a plausible role(s) for IREF-2 during the initiation processes of vRNA replication is discussed.
Medical subject headings
- Host-Pathogen Interactions
- Intracellular Signaling Peptides and Proteins
- Orthomyxoviridae
- RNA, Complementary
- RNA, Viral
- Tumor Necrosis Factor Ligand Superfamily Member 13
- Virus Replication