Functional characterization of Nicotiana benthamiana homologs of peanut water deficit-induced genes by virus-induced gene silencing

Planta ◽  
2006 ◽  
Vol 225 (3) ◽  
pp. 523-539 ◽  
Author(s):  
M. Senthil-Kumar ◽  
Geetha Govind ◽  
Li Kang ◽  
Kirankumar S. Mysore ◽  
M. Udayakumar
2010 ◽  
Vol 48 (1) ◽  
pp. 35-44 ◽  
Author(s):  
Muthappa Senthil-Kumar ◽  
Ramanna Hema ◽  
Thumu Rao Suryachandra ◽  
H.V. Ramegowda ◽  
Ramaswamy Gopalakrishna ◽  
...  

2005 ◽  
Vol 138 (4) ◽  
pp. 2155-2164 ◽  
Author(s):  
Ingo Hein ◽  
Maria Barciszewska-Pacak ◽  
Katarina Hrubikova ◽  
Sandie Williamson ◽  
Malene Dinesen ◽  
...  

2019 ◽  
Vol 74 (5-6) ◽  
pp. 151-159
Author(s):  
Feng Zhu ◽  
Yanping Che ◽  
Fei Xu ◽  
Yangkai Zhou ◽  
Kun Qian ◽  
...  

Abstract Virus-induced gene silencing (VIGS) is an effective strategy for rapid gene function analysis. It is well established that the NAC transcription factor and salicylic acid (SA) signal pathway play essential roles in response to biotic stresses. However, simultaneous silencing of two target genes using VIGS in plants has been rarely reported. Therefore, in this report, we performed VIGS to silence simultaneously the SA-binding protein 2 (NbSABP2) and NbNAC1 in Nicotiana benthamiana to investigate the gene silencing efficiency of simultaneous silencing of two genes. We first cloned the full-length NbNAC1 gene, and the characterization of NbNAC1 was also analysed. Overlap extension polymerase chain reaction (PCR) analysis showed that the combination of NbSABP2 and NbNAC1 was successfully amplified. Bacteria liquid PCR confirmed that the combination of NbSABP2 and NbNAC1 was successfully inserted into the tobacco rattle virus vector. The results showed that the leaves from the NbSABP2 and NbNAC1 gene-silenced plants collapsed slightly, with browning at the base of petiole or veina. Quantitative real-time PCR results showed that the expression of NbSABP2 and NbNAC1 were significantly reduced in 12 days post silenced plants after tobacco rattle virus infiltration compared with the control plants. Overall, our results suggest that VIGS can be used to silence simultaneously two target genes.


2010 ◽  
Vol 189 (2) ◽  
pp. 471-483 ◽  
Author(s):  
Karina van der Linde ◽  
Christine Kastner ◽  
Jochen Kumlehn ◽  
Regine Kahmann ◽  
Gunther Doehlemann

2020 ◽  
Author(s):  
Liyun Song ◽  
Jie Wang ◽  
Haiyan Jia ◽  
Ali Kamran ◽  
Yuanxia Qin ◽  
...  

Abstract Background: Major latex proteins (MLPs) belong to the MLP subfamily in Bet v 1 protein family and respond to both biotic and abiotic stresses, which play critical roles in plant disease resistance. As the type species of widely distributed and economically devastating Potyvirus, Potato virus Y (PVY) is one of the major constraints to important crop plants including tobacco ( Nicotiana benthamiana ) worldwide. Despite the great losses owing to PVY infection in tobacco, there is no previous study investigating the potential role of MLPs in developing resistance to viral infection. Results: In this study, for the first time we have identified and functionally analyzed the MLP-like protein 28 from N. benthamiana , denoted as NbMLP28 and investigated its role in conferring resistance to N. benthamiana against PVY infection. NbMLP28 was localized to the plasmalemma and nucleus, with the highest level in the root. NbMLP28 gene was hypothesized to be triggered by PVY infection and was highly expressed in jasmonic acid (JA) signaling pathway. Further validation was achieved through silencing of NbMLP28 through virus-induced gene silencing (VIGS) that rendered N. benthamiana plants more vulnerable to PVY infection, contrary to overexpression that enhanced resistance. Conclusions: Taken together, this is the first study describing the role of NbMLP28 in tobacco against PVY infection and provide a pivotal point towards obtaining pathogen-resistant tobacco varieties through constructing new candidate genes of MLP subfamily.


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