The McInerney Laboratory at Karolinska Institutet, Stockholm, Sweden
In vivo labeling of nascent viral RNA with BrUTP
Text and figure adapted from (Panas et al., 2015)
Since the function of SGs appears linked to the triage of mRNA, it is reasonable to assume that SGs induced during viral infection might sequester viral mRNAs in order to inhibit their translation. To examine the relationship between viral RNA replication complexes and SGs, it is useful to visualize nascent viral RNA in situ and co-stain for SG marker(s). A number of techniques are available for co-staining RNA and protein including 5-bromourudine 5’-triphosphate (BrUTP) labeling. BrUTP labeling involves incubating cells with modified ribonucleotide BrUTP to allow its incorporation into nascent RNA, followed by the immunodetection of BrUTP using a specific antibody (Enzo) (Restrepo-Hartwig and Ahlquist, 1996). BrUTP uptake into cells is facilitated by transfection. This technique allows the detection of viral RNAs, which may be localized to SGs during infection. Its major advantage over conventional in situ hybridization and dsRNA staining, if used together with actinomycin D (Act D; see below) to block host cellular transcription, it is selective for newly synthesized viral RNA produced during short times during infection. In our previous work (McInerney et al., 2005), we used in vivo BrUTP labeling to identify nascent SFV RNA in combination with TIA-1 immunostaining to identify SGs. We found that, when present in virus-infected cells, the SGs were typically located in regions of the cell devoid of newly produced viral RNA. As the infection progressed, and viral replication complexes were distributed throughout the cytoplasm, SGs were no longer detectable. We did not detect BrUTP labelled viral RNA in SGs, in agreement with FISH results that did not detect viral RNA in SGs.
Alphavirus infection profoundly inhibits the synthesis of cellular RNA (Gorchakov et al., 2005). Short times after infection, pulse-labeled RNA will consist almost entirely of viral RNA (Breakwell et al., 2007; Gorchakov et al., 2005). However, for other RNA viruses, BrUTP staining may label both viral and cellular RNA, confounding interpretation of staining. Since viral RNA-dependent RNA polymerases are not sensitive to actinomycin D (Act D), this inhibitor can be used during BrUTP labeling to ensure that only viral RNAs incorporate the BrUTP. Act D inhibits DNA-dependent transcription by binding DNA template and preventing mRNA elongation by RNA polymerases, but does not bind RNA. Figure A shows MEFs after staining with BrUTP for 1 hour in the presence or absence of Act D. In non Act D-treated cells, BrUTP staining is brightest in the nucleoli, the sites of ribosomal RNA synthesis. Different intensities of BrUTP staining reflect different efficiencies of transfection of the nucleotide in individual cells.
We infected MEFs with wt SFV at MOI 0.5, and labeled total RNA using a 1-hr incubation with BrUTP in the presence of Act D (between 4 and 5 hpi; Figure B). Under these conditions, no RNA staining was detected in nucleoli. In cells where SGs were visible, nascent viral RNA staining was always located contralateral to the TIA-1-positive SGs. A representative image is shown.
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