scholarly journals Virus-Induced Gene Silencing as a Tool for Comparative Functional Studies in Thalictrum

PLoS ONE ◽  
2010 ◽  
Vol 5 (8) ◽  
pp. e12064 ◽  
Author(s):  
Verónica S. Di Stilio ◽  
Rachana A. Kumar ◽  
Alessandra M. Oddone ◽  
Theadora R. Tolkin ◽  
Patricia Salles ◽  
...  
2019 ◽  
Author(s):  
Zhiquan Wang ◽  
Xiaoyang Xu ◽  
Longjie Ni ◽  
Jinbo Guo ◽  
Chunsun Gu

Background. Hibiscus hamabo Sieb. et Zucc. is a semi-mangrove plant used for the ecological restoration of saline-alkali land, coastal afforestation and urban landscaping. Because the genetic transformation of H. hamabo is difficult, molecular breeding and gene functional studies have been severely restricted. In plants, virus-induced gene silencing provides a pathway to rapidly and effectively create targeted gene knockouts for gene functional studies. Methods. In this study, we tested the efficiency of a Tobacco rattle virus vector in silencing the cloroplastos alterados 1 (CLA1) gene through agroinfiltration. Results. The leaves of H. hamabo showed white streaks typical of CLA1 gene silencing three weeks after agroinfiltration. In agroinfiltrated H. hamabo plants, the CLA1 expression levels in leaves with white streaks were all significantly lower than in those of mock-infected and control plants. Conclusions. Thus, this virus-induced gene silencing system was efficient in H. hamabo and may be a powerful tool for large-scale reverse-genetic analyses of gene functions in H. hamabo.


PeerJ ◽  
2019 ◽  
Vol 7 ◽  
pp. e7505 ◽  
Author(s):  
Zhiquan Wang ◽  
Xiaoyang Xu ◽  
Longjie Ni ◽  
Jinbo Guo ◽  
Chunsun Gu

Background Hibiscus hamabo Sieb. et Zucc. is a semi-mangrove plant used for the ecological restoration of saline-alkali land, coastal afforestation and urban landscaping. The genetic transformation H. hamabo is currently inefficient and laborious, restricting gene functional studies on this species. In plants, virus-induced gene silencing provides a pathway to rapidly and effectively create targeted gene knockouts for gene functional studies. Methods In this study, we tested the efficiency of a tobacco rattle virus vector in silencing the cloroplastos alterados 1 (CLA1) gene through agroinfiltration. Results The leaves of H. hamabo showed white streaks typical of CLA1 gene silencing three weeks after agroinfiltration. In agroinfiltrated H. hamabo plants, the CLA1 expression levels in leaves with white streaks were all significantly lower than those in leaves from mock-infected and control plants. Conclusions The system presented here can efficiently silence genes in H. hamabo and may be a powerful tool for large-scale reverse-genetic analyses of gene functions in H. hamabo.


2021 ◽  
Vol 9 (5) ◽  
Author(s):  
Shane Carey ◽  
Mónica Higuera‐Díaz ◽  
Peter Mankowski ◽  
Alexandra Rocca ◽  
Jocelyn C. Hall

2013 ◽  
Vol 33 (2) ◽  
pp. 301-312 ◽  
Author(s):  
Xionghui Zhong ◽  
Xue Yuan ◽  
Ze Wu ◽  
Muhammad Ali Khan ◽  
Jin Chen ◽  
...  

2019 ◽  
Author(s):  
Zhiquan Wang ◽  
Xiaoyang Xu ◽  
Longjie Ni ◽  
Jinbo Guo ◽  
Chunsun Gu

Background. Hibiscus hamabo Sieb. et Zucc. is a semi-mangrove plant used for the ecological restoration of saline-alkali land, coastal afforestation and urban landscaping. Because the genetic transformation of H. hamabo is difficult, molecular breeding and gene functional studies have been severely restricted. In plants, virus-induced gene silencing provides a pathway to rapidly and effectively create targeted gene knockouts for gene functional studies. Methods. In this study, we tested the efficiency of a Tobacco rattle virus vector in silencing the cloroplastos alterados 1 (CLA1) gene through agroinfiltration. Results. The leaves of H. hamabo showed white streaks typical of CLA1 gene silencing three weeks after agroinfiltration. In agroinfiltrated H. hamabo plants, the CLA1 expression levels in leaves with white streaks were all significantly lower than in those of mock-infected and control plants. Conclusions. Thus, this virus-induced gene silencing system was efficient in H. hamabo and may be a powerful tool for large-scale reverse-genetic analyses of gene functions in H. hamabo.


BIO-PROTOCOL ◽  
2015 ◽  
Vol 5 (12) ◽  
Author(s):  
Lokanadha Gunupuru ◽  
Shahin Ali ◽  
Fiona Doohan ◽  
Steven Scofield

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Yuh Tzean ◽  
Ming-Chi Lee ◽  
Hsiao-Hsuan Jan ◽  
Yi-Shu Chiu ◽  
Tsui-Chin Tu ◽  
...  

Plant Methods ◽  
2021 ◽  
Vol 17 (1) ◽  
Author(s):  
Decai Tuo ◽  
Peng Zhou ◽  
Pu Yan ◽  
Hongguang Cui ◽  
Yang Liu ◽  
...  

Abstract Background Cassava is an important crop for food security and industry in the least-developed and developing countries. The completion of the cassava genome sequence and identification of large numbers of candidate genes by next-generation sequencing provide extensive resources for cassava molecular breeding and increase the need for rapid and efficient gene function analysis systems in cassava. Several plant virus-induced gene silencing (VIGS) systems have been developed as reverse genetic tools for rapid gene function analysis in cassava. However, these VIGS vectors could cause severe viral symptoms or inefficient gene silencing. Results In this study, we constructed agroinfection-compatible infectious cDNA clones of cassava common mosaic virus isolate CM (CsCMV-CM, genus Potexvirus, family Alphaflexiviridae) that causes systemic infection with mild symptoms in cassava. CsCMV-CM was then modified to a viral vector carrying the Nimble cloning frame, which facilitates the rapid and high-throughput cloning of silencing fragments into the viral genome. The CsCMV-based vector successfully silenced phytoene desaturase (PDS) and magnesium chelatase subunit I (ChlI) in different cassava varieties and Nicotiana benthamiana. The silencing of the ChlI gene could persist for more than two months. Conclusions This CsCMV-based VIGS system provides a new tool for rapid and efficient gene function studies in cassava.


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