Premium
Live‐cell imaging of viral RNA genomes using a Pumilio‐based reporter
Author(s) -
Tilsner Jens,
Linnik Olga,
Christensen Nynne M.,
Bell Karen,
Roberts Ian M.,
Lacomme Christophe,
Oparka Karl J.
Publication year - 2009
Publication title -
the plant journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.058
H-Index - 269
eISSN - 1365-313X
pISSN - 0960-7412
DOI - 10.1111/j.1365-313x.2008.03720.x
Subject(s) - rna , genome , biology , cell , virology , computational biology , live cell imaging , genetics , gene
Summary We describe a method for localizing plant viral RNAs in vivo using Pumilio, an RNA‐binding protein, coupled to bimolecular fluorescence complementation (BiFC). Two Pumilio homology domain (PUMHD) polypeptides, fused to either the N‐ or C‐terminal halves of split mCitrine, were engineered to recognize two closely adjacent eight‐nucleotide sequences in the genomic RNA of tobacco mosaic virus (TMV). Binding of the PUMHDs to their target sites brought the split mCitrine halves into close proximity, allowing BiFC to occur and revealing the localization of viral RNA within infected cells. The bulk of the RNA was sequestered in characteristic inclusion bodies known as viral replication complexes (VRCs), with a second population of RNA localized in discrete particles distributed throughout the peripheral cytoplasm. Transfer of the TMV Pumilio recognition sequences into the genome of potato virus X (PVX) allowed the PVX RNA to be localized. Unlike TMV, the PVX RNA was concentrated in distinctive ‘whorls’ within the VRC. Optical sectioning of the PVX VRCs revealed that one of the viral movement proteins was localized to the centres of the RNA whorls, demonstrating significant partitioning of viral RNA and proteins within the VRC. The utility of Pumilio as a fluorescence‐based reporter for viral RNA is discussed.