Two key arginine residues in the coat protein of Bamboo mosaic virus differentially affect the accumulation of viral genomic and subgenomic RNAs
Summary The interactions between viral RNAs and coat proteins (CPs) are critical for the efficient completion of infection cycles of RNA viruses. However, the specificity of the interactions between CPs and genomic or subgenomic RNAs remains poorly understood. In this study, Bamboo mosaic virus (BaM...
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Published in | Molecular plant pathology Vol. 15; no. 2; pp. 196 - 210 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Blackwell Publishing Ltd
01.02.2014
John Wiley & Sons, Inc John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Summary
The interactions between viral RNAs and coat proteins (CPs) are critical for the efficient completion of infection cycles of RNA viruses. However, the specificity of the interactions between CPs and genomic or subgenomic RNAs remains poorly understood. In this study, Bamboo mosaic virus (BaMV) was used to analyse such interactions. Using reversible formaldehyde cross‐linking and mass spectrometry, two regions in CP, each containing a basic amino acid (R99 and R227, respectively), were identified to bind directly to the 5′ untranslated region of BaMV genomic RNA. Analyses of the alanine mutations of R99 and R227 revealed that the secondary structures of CP were not affected significantly, whereas the accumulation of BaMV genomic, but not subgenomic, RNA was severely decreased at 24 h post‐inoculation in the inoculated protoplasts. In the absence of CP, the accumulation levels of genomic and subgenomic RNAs were decreased to 1.1%–1.5% and 33%–40% of that of the wild‐type (wt), respectively, in inoculated leaves at 5 days post‐inoculation (dpi). In contrast, in the presence of mutant CPs, the genomic RNAs remained about 1% of that of wt, whereas the subgenomic RNAs accumulated to at least 87%, suggesting that CP might increase the accumulation of subgenomic RNAs. The mutations also restricted viral movement and virion formation in Nicotiana benthamiana leaves at 5 dpi. These results demonstrate that R99 and R227 of CP play crucial roles in the accumulation, movement and virion formation of BaMV RNAs, and indicate that genomic and subgenomic RNAs interact differently with BaMV CP. |
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Bibliography: | National Science Council, Taiwan, Republic of China - No. NSC-101-2313-B-005-036-MY3; No. NSC-97-2752-B-005-005-PAE istex:B46659262E20E02F300C9D1E667C9D8394624233 ark:/67375/WNG-X6SW7G3S-D Fig. S1 Alignment of coat protein (CP) amino acid sequences of nine different potexviruses. The alignment was performed using the software ClustalW (Thompson et al., 2002) with the default parameters. The putative RNA-binding motif (Tremblay et al., 2006) is underlined. The amino acids of Papaya mosaic virus (PapMV) (Tremblay et al., 2006) and Bamboo mosaic virus (BaMV) involved in RNA binding are indicated by open and filled stars, respectively. The amino acid sequences of the CPs of the nine potexviruses extensively characterized were selected from GenBank (Benson et al., 2013). The abbreviations and accession numbers are as follows: PAMV, Potato aucuba mosaic virus (gi|20177423); CymMV, Cymbidium mosaic virus (gi|46309858); ScaVX, Scallion virus X (gi|18652423); PVX, Potato virus X (gi|872290); HrV, Hydrangea ringspot virus (gi|62326909); CcMV, Cassava common mosaic virus (gi|9628112); PapMV, Papaya mosaic virus (gi|9629172); FoMV, Foxtail mosaic virus (gi|158268262); BaMV, Bamboo mosaic virus (gi|13182723). Fig. S2 Comparison of the RNA-binding sites in the Bamboo mosaic virus (BaMV) and Papaya mosaic virus (PapMV) coat protein (CP) structure. The structure of BaMV CP was modelled using the crystal structure of PapMV (PDB accession number 4DOX) as the template in the Phyre2 server (Kelley and Sternberg, 2009). The RNA-binding residues of PapMV (K97) and BaMV (R99) CP are indicated by the arrows. Table S1 The primers used in this study. ArticleID:MPP12080 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 |
ISSN: | 1464-6722 1364-3703 |
DOI: | 10.1111/mpp.12080 |