Implication of the C terminus of the Prunus necrotic ringspot virus movement protein in cell-to-cell transport and in its interaction with the coat protein

2010 ◽  
Vol 91 (7) ◽  
pp. 1865-1870 ◽  
Author(s):  
F. Aparicio ◽  
V. Pallas ◽  
J. Sanchez-Navarro
2013 ◽  
Vol 94 (3) ◽  
pp. 677-681 ◽  
Author(s):  
Thor V. M. Fajardo ◽  
Ana Peiró ◽  
Vicente Pallás ◽  
Jesús Sánchez-Navarro

We previously showed that the movement protein (MP) gene of Alfalfa mosaic virus (AMV) is functionally exchangeable for the cell-to-cell transport of the corresponding genes of Tobacco mosaic virus (TMV), Brome mosaic virus, Prunus necrotic ringspot virus, Cucumber mosaic virus and Cowpea mosaic virus. We have analysed the capacity of the heterologous MPs to systemically transport the corresponding chimeric AMV genome. All MPs were competent in systemic transport but required the fusion at their C terminus of the coat protein-interacting C-terminal 44 aa (A44) of the AMV MP. Except for the TMV MP, the presence of the hybrid virus in upper leaves correlated with the capacity to move locally. These results suggest that all the MPs assigned to the 30K superfamily should be exchangeable not only for local virus movement but also for systemic transport when the A44 fragment is present.


2004 ◽  
Vol 85 (4) ◽  
pp. 1039-1048 ◽  
Author(s):  
Katalin Salánki ◽  
Ákos Gellért ◽  
Emese Huppert ◽  
Gábor Náray-Szabó ◽  
Ervin Balázs

For the cell-to-cell movement of cucumoviruses both the movement protein (MP) and the coat protein (CP) are required. These are not reversibly exchangeable between Cucumber mosaic virus (CMV) and Tomato aspermy virus (TAV). The MP of CMV is able to function with the TAV CP (chimera RT), but TAV MP is unable to promote the cell-to-cell movement in the presence of CMV CP (chimera TR). To gain further insight into the non-infectious nature of the TR recombinant, RNA 3 chimeras were constructed with recombinant MPs and CPs. The chimeric MP and one of the CP recombinants were infectious. The other recombinant CP enabled virus movement only after the introduction of two point mutations (Glu→Lys and Lys→Arg at aa 62 and 65, respectively). The mutations served to correct the CP surface electrostatic potential that was altered by the recombination. The infectivity of the TR virus on different test plants was restored by replacing the sequence encoding the C-terminal 29 aa of the MP with the corresponding sequence of the CMV MP gene or by exchanging the sequence encoding the C-terminal 15 aa of the CP with the same region of TAV. The analysis of the recombinant clones suggests a requirement for compatibility between the C-terminal 29 aa of the MP and the C-terminal two-thirds of the CP for cell-to-cell movement of cucumoviruses.


2003 ◽  
Vol 148 (2) ◽  
pp. 265-279 ◽  
Author(s):  
P. Bertens ◽  
W. Heijne ◽  
N. Van der Wel ◽  
J. Wellink ◽  
A. Van Kammen

2008 ◽  
Vol 153 (5) ◽  
pp. 909-919 ◽  
Author(s):  
Nicola Fiore ◽  
Thor V. M. Fajardo ◽  
Simona Prodan ◽  
María Carmen Herranz ◽  
Frederic Aparicio ◽  
...  

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