Establishment of transgenic lettuce plants producing potentially antihypertensive ShRNA
- Autores: Gerasymenko I.M.1, Kleschevnikov V.V.2, Kedlian V.R.2, Sakhno L.O.1, Arbuzova I.A.1, Sheludko Y.V.1, Dosenko V.E.2, Kuchuk N.V.1
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Afiliações:
- Institute of Cell Biology and Genetic Engineering
- Bogomoletz Institute of Physiology
- Edição: Volume 51, Nº 1 (2017)
- Páginas: 1-7
- Seção: Article
- URL: https://journals.rcsi.science/0095-4527/article/view/173509
- DOI: https://doi.org/10.3103/S0095452717010054
- ID: 173509
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Resumo
Development of RNAi-based therapeutics is a fast growing field of the pharmaceutical industry. Using plants for production of pharmaceutically valuable siRNAs may have significant advantages of costeffectiveness, scalability, and low risk of contamination with human pathogens. If edible plant species are genetically engineered to synthesize siRNAs, the costly stage of target product purification may be omitted. We describe the establishment of transgenic lettuce plants producing shRNA targeting delta isoform of protein kinase C (PKC-delta), an effective target for RNAi-based treatment of arterial hypertension. Transgenic lettuce plants were obtained by Agrobacterium-mediated transformation with genetic constructs harboring antiPKC and scrambled (control) shRNA genes. The presence of transgenes was proven by PCR analysis, and the accumulation of antiPKC shRNA was estimated using the RT-qPCR technique. Six transgenic lettuce lines showed varying levels of antiPKC shRNA expression with the highest value reaching 14 ± 9% of highly abundant endogenous lettuce micro RNA (miR156a), or 12.7 fmol/g dry weight. Plants carrying either antiPKC or scrambled shRNA genes flowered normally but did not produce seeds. The described transgenic lettuce plants accumulating antiPKC siRNA are the subject for animal testing and can be considered as raw material for the development of novel antihypertensive drugs.
Sobre autores
I. Gerasymenko
Institute of Cell Biology and Genetic Engineering
Autor responsável pela correspondência
Email: i-gerasimenko@ukr.net
Ucrânia, Kyiv
V. Kleschevnikov
Bogomoletz Institute of Physiology
Email: i-gerasimenko@ukr.net
Ucrânia, Kyiv
V. Kedlian
Bogomoletz Institute of Physiology
Email: i-gerasimenko@ukr.net
Ucrânia, Kyiv
L. Sakhno
Institute of Cell Biology and Genetic Engineering
Email: i-gerasimenko@ukr.net
Ucrânia, Kyiv
I. Arbuzova
Institute of Cell Biology and Genetic Engineering
Email: i-gerasimenko@ukr.net
Ucrânia, Kyiv
Y. Sheludko
Institute of Cell Biology and Genetic Engineering
Email: i-gerasimenko@ukr.net
Ucrânia, Kyiv
V. Dosenko
Bogomoletz Institute of Physiology
Email: i-gerasimenko@ukr.net
Ucrânia, Kyiv
N. Kuchuk
Institute of Cell Biology and Genetic Engineering
Email: i-gerasimenko@ukr.net
Ucrânia, Kyiv
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