A 5′P degradation hot spot influences molecular farming of anticancerogenic nuclease TBN1 in tobacco cells

• Published in: Plant cell, tissue and organ culture Vol. 127; no. 2; pp. 347 - 358
• Main Authors: Týcová, Anna, Piernikarczyk, Rajen J. J., Kugler, Michael, Lipovová, Petra, Podzimek, Tomáš, Steger, Gerhard, Matoušek, Jaroslav
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer Netherlands 01.11.2016; Springer Nature B.V
• Subjects: Biomedical and Life Sciences; Biotechnology; Cell culture; Cell fusion; Degradation; Farming; Fluorescence; Fusion protein; Gene expression; Leaves; Life Sciences; mRNA; Nuclease; Original Article; Plant cells; Plant Genetics and Genomics; Plant Pathology; Plant Physiology; Plant Sciences; Plants (botany); Proteins; Ribonucleic acid; RNA; Suppressors; Suspension culture; Tobacco; Tomatoes; siRNA; mRNA quantification; Post-transcriptional gene silencing; Plant nuclease I
• ISSN: 0167-6857; 1573-5044
• DOI: 10.1007/s11240-016-1054-x

Tomato bifunctional nuclease 1 (TBN1) is a polyfunctional protein with anticancerogenic activity originally isolated as an overexpressed protein from viroid-infected tomato. Its molecular farming in plant cells could be a non-expensive source for its biotechnology preparation. So we analysed TBN1 expression in Agrobacterium -infiltrated leaf sectors of Nicotiana benthamiana and in transformed suspension culture of tobacco BY-2 cells. During its transient expression, TBN1 mRNA was strongly degraded within a hot spot localized in the 3′ region. This early degradation process was inhibited by PTGS suppressors p19 and p38 resulting in increased TBN1 mRNA and protein yield. In parallel to degradation of TBN1 mRNA, high mRNA levels of two RNA-dependent RNA polymerases were detected in infiltrated leaf sectors, as well as in the transformed tobacco suspension culture BY-2, where low expression of the nuclease was stably maintained. Higher TBN1 mRNA and nuclease activity levels were found during its molecular farming in RDR6-deficient N. benthamiana plants. By fluorescent microscopy of infiltrated and transformed plant cells, the nuclease-GFP fusion protein was shown to be organized in filament-like structures.