Efficient transient expression of human GM-CSF protein in Nicotiana benthamiana using potato virus X vector

2006 ◽  
Vol 72 (4) ◽  
pp. 756-762 ◽  
Author(s):  
Fengyong Zhou ◽  
Ming-Li Wang ◽  
Henrik H. Albert ◽  
Paul H. Moore ◽  
Yun J. Zhu
2003 ◽  
Vol 21 (7) ◽  
pp. 699-704 ◽  
Author(s):  
C. Escobar ◽  
L. E. Hernández ◽  
A. Jiménez ◽  
G. Creissen ◽  
M. T. Ruiz ◽  
...  

2008 ◽  
Vol 58 (1) ◽  
pp. 154-161 ◽  
Author(s):  
Noemi Čeřovská ◽  
Hana Hoffmeisterová ◽  
Tamara Pečenková ◽  
Tomáš Moravec ◽  
Helena Synková ◽  
...  

2020 ◽  
Vol 276 ◽  
pp. 197823
Author(s):  
Gabriel Robles-Luna ◽  
Nicolás Furman ◽  
María Florencia Barbarich ◽  
Nicolás Carlotto ◽  
Alejandra Attorresi ◽  
...  

2008 ◽  
Vol 21 (2) ◽  
pp. 178-187 ◽  
Author(s):  
Shahid Aslam Siddiqui ◽  
Cecilia Sarmiento ◽  
Erkki Truve ◽  
Harry Lehto ◽  
Kirsi Lehto

RNA silencing suppressor genes derived from six virus genera were transformed into Nicotiana benthamiana and N. tabacum plants. These suppressors were P1 of Rice yellow mottle virus (RYMV), P1 of Cocksfoot mottle virus, P19 of Tomato bushy stunt virus, P25 of Potato virus X, HcPro of Potato virus Y (strain N), 2b of Cucumber mosaic virus (strain Kin), and AC2 of African cassava mosaic virus (ACMV). HcPro caused the most severe phenotypes in both Nicotiana spp. AC2 also produced severe effects in N. tabacum but a much milder phenotype in N. benthamiana, although both HcPro and AC2 affected the leaf tissues of the two Nicotiana spp. in similar ways, causing hyperplasia and hypoplasia, respectively. P1-RYMV caused high lethality in the N. benthamiana plants but only mild effects in the N. tabacum plants. Phenotypic alterations produced by the other transgenes were minor in both species. Interestingly, the suppressors had very different effects on crucifer-infecting Tobamovirus (crTMV) infections. AC2 enhanced both spread and brightness of the crTMV-green fluorescent protein (GFP) lesions, whereas 2b and both P1 suppressors enhanced spread but not brightness of these lesions. P19 promoted spread of the infection into new foci within the infiltrated leaf, whereas HcPro and P25 suppressed the spread of crTMV-GFP lesions.


Virology ◽  
2000 ◽  
Vol 275 (2) ◽  
pp. 444-451 ◽  
Author(s):  
Carol A. Plante ◽  
Kook-Hyung Kim ◽  
Neeta Pillai-Nair ◽  
Toba A.M. Osman ◽  
Kenneth W. Buck ◽  
...  

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Ran Li ◽  
Chuan-Sia Tee ◽  
Yu-Lin Jiang ◽  
Xi-Yuan Jiang ◽  
Prasanna Nori Venkatesh ◽  
...  

2010 ◽  
Vol 23 (4) ◽  
pp. 376-383 ◽  
Author(s):  
Thierry Candresse ◽  
Armelle Marais ◽  
Chantal Faure ◽  
Marie Pierre Dubrana ◽  
Julie Gombert ◽  
...  

Despite the fact that Pepino mosaic virus (PepMV) and Potato virus X (PVX) share less than 40% identity in their coat proteins (CP), the known PVX elicitor of Rx, transgenic tomato (cv. Microtom) plants expressing a functional potato Rx resistance gene showed resistance toward PepMV. However, in a low percentage of plants, PepMV accumulation was observed and back inoculation experiments demonstrated that these plants contained resistance-breaking PepMV variants. Sequencing of the CP gene of these variants showed the accumulation of mutations in the amino acid 41 to 125 region the CP, whereas no mutations were observed in the nonevolved isolates. Agroinfiltration-mediated transient expression of the mutant CP demonstrated that they had a greatly attenuated or abolished ability to induce a hypersensitive reaction in Rx-expressing Nicotiana benthamiana leaves. The transient expression of truncated forms of the PepMV CP allowed the identification of a minimal elicitor domain (amino acids 30 to 136). These results demonstrate that the Rx-based sensing system is able to recognize the PepMV CP but, contrary to the situation with PVX, for which only two closely spaced resistance-breaking mutations are known, many mutations over a significant stretch of the PepMV CP allow escape from recognition by Rx.


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