Induced expression of Serratia marcescens ribonuclease III gene in transgenic Nicotiana tabacum L. cv. SR1 tobacco plants
- Authors: Zhirnov I.V.1, Trifonova E.A.1, Romanova A.V.1, Filipenko E.A.1, Sapotsky M.V.2, Malinovsky V.I.2, Kochetov A.V.1,3, Shumny V.K.1,3
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Affiliations:
- Federal Research Center Institute of Cytology and Genetics, Siberian Branch
- Institute of Biology and Soil Science, Far East Branch
- Department of Cytology and Genetics
- Issue: Vol 52, No 11 (2016)
- Pages: 1137-1141
- Section: Plant Genetics
- URL: https://journal-vniispk.ru/1022-7954/article/view/187971
- DOI: https://doi.org/10.1134/S102279541611017X
- ID: 187971
Cite item
Abstract
Transgenic Nicotiana tabacum L. cv. SR1 plants, characterized by an increase in the level of dsRNA-specific hydrolytic activity after induction by wounding, were obtained. The Solanum lycopersicum anionic peroxidase gene promoter (new for plant genetic engineering) was for the first time used for the induced expression of the target Serratia marcescens RNase III gene. Upon infection with the tobacco mosaic virus (TMV), the transgenic plants of the obtained lines did not differ significantly from the control group in the level of TMV capsid protein accumulation. In general, no delay in the development of the infection symptoms was observed in transgenic plants as compared with the control group. The obtained transgenic plants represent a new model for the study of the biological role of endoribonucleases from the RNase III family, including in molecular mechanisms of resistance to pathogens.
About the authors
I. V. Zhirnov
Federal Research Center Institute of Cytology and Genetics, Siberian Branch
Author for correspondence.
Email: zh@bionet.nsc.ru
Russian Federation, Novosibirsk, 630090
E. A. Trifonova
Federal Research Center Institute of Cytology and Genetics, Siberian Branch
Email: zh@bionet.nsc.ru
Russian Federation, Novosibirsk, 630090
A. V. Romanova
Federal Research Center Institute of Cytology and Genetics, Siberian Branch
Email: zh@bionet.nsc.ru
Russian Federation, Novosibirsk, 630090
E. A. Filipenko
Federal Research Center Institute of Cytology and Genetics, Siberian Branch
Email: zh@bionet.nsc.ru
Russian Federation, Novosibirsk, 630090
M. V. Sapotsky
Institute of Biology and Soil Science, Far East Branch
Email: zh@bionet.nsc.ru
Russian Federation, Vladivostok, 690022
V. I. Malinovsky
Institute of Biology and Soil Science, Far East Branch
Email: zh@bionet.nsc.ru
Russian Federation, Vladivostok, 690022
A. V. Kochetov
Federal Research Center Institute of Cytology and Genetics, Siberian Branch; Department of Cytology and Genetics
Email: zh@bionet.nsc.ru
Russian Federation, Novosibirsk, 630090; Novosibirsk, 630090
V. K. Shumny
Federal Research Center Institute of Cytology and Genetics, Siberian Branch; Department of Cytology and Genetics
Email: zh@bionet.nsc.ru
Russian Federation, Novosibirsk, 630090; Novosibirsk, 630090
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