Identification and characterization of pectin related gene NbGAE6 through virus-induced gene silencing in Nicotiana benthamiana

Gene ◽  
2020 ◽  
Vol 741 ◽  
pp. 144522
Author(s):  
Rana Imtiaz Ahmed ◽  
Angyan Ren ◽  
Dahai Yang ◽  
Anming Ding ◽  
Yingzhen Kong
2016 ◽  
Vol 80 (3) ◽  
pp. 355-366 ◽  
Author(s):  
Baniekal Hiremath Gangadhar ◽  
Kappachery Sajeesh ◽  
Jelli Venkatesh ◽  
Venkidasamy Baskar ◽  
Kumar Abhinandan ◽  
...  

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.


Planta ◽  
2006 ◽  
Vol 225 (3) ◽  
pp. 523-539 ◽  
Author(s):  
M. Senthil-Kumar ◽  
Geetha Govind ◽  
Li Kang ◽  
Kirankumar S. Mysore ◽  
M. Udayakumar

Genomics ◽  
1999 ◽  
Vol 59 (1) ◽  
pp. 51-58 ◽  
Author(s):  
Sandro Banfi ◽  
Maria Teresa Bassi ◽  
Grazia Andolfi ◽  
Anna Marchitiello ◽  
Stefania Zanotta ◽  
...  

2019 ◽  
Author(s):  
Mei Liu ◽  
Zhiling Liang ◽  
Miguel A. Aranda ◽  
Ni Hong ◽  
Liming Liu ◽  
...  

AbstractCucurbits produce fruits or vegetables that have great dietary importance and economic significance worldwide. The published genomes of at least 11 cucurbit species are boosting gene mining and novel breeding strategies, however genetic transformation in cucurbits is impractical as a tool for gene function validation due to low transformation efficiencies. Virus-induced gene silencing (VIGS) is a potential alternative tool. So far, very few ideal VIGS vectors are available for cucurbits. Here, we describe a new VIGS vector derived from cucumber green mottle mosaic virus (CGMMV), a monopartite virus that infects cucurbits naturally. We show that the CGMMV vector is competent to induce efficient silencing of the phytoene desaturase (PDS) gene in the model plant Nicotiana benthamiana and in cucurbits, including watermelon, melon, cucumber and bottle gourd. Infection with the CGMMV vector harboring PDS sequences of 69-300 bp in length in the form of sense-oriented or hairpin cDNAs resulted in photobleaching phenotypes in N. benthamiana and cucurbits by PDS silencing. Additional results reflect that silencing of the PDS gene could persist for over two months and the silencing effect of CGMMV-based vectors could be passaged. These results demonstrate that CGMMV vector could serve as a powerful and easy-to-use tool for characterizing gene function in cucurbits.One sentence summaryA CGMMV-based vector enables gene function studies in cucurbits, an extremely low efficiency species for genetic transformation.


Neurosurgery ◽  
2000 ◽  
Vol 47 (2) ◽  
pp. 518-518
Author(s):  
Gregory D. Foltz ◽  
Abel Jarell ◽  
Jim Schuster ◽  
Masazumi Matsumura ◽  
Lindi Farrell ◽  
...  

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