Abstract

BackgroundNowadays, the challenge for biotechnology is to develop tools for agriculture and industry to provide plants characterized by productivity and quality that will satisfy the growing demand for different kinds of natural products. To meet the challenge, the generation and application of genetically modified plants is justified. However, the strong social resistance to genetically modified organisms and restrictive regulations in European Union countries necessitated the development of a new technology for new plant types generation which uses the knowledge resulting from analysis of genetically modified plants to generate favourably altered plants while omitting the introduction of heterologous genes to their genome. Four-year experiments led to the development of a technology inducing heritable epigenetic gene activation without transgenesis.ResultsThe method comprises the induction of changes in methylation/demethylation of the endogenous gene by the plant’s treatment with short oligodeoxynucleotides antisense to the coding region. In vitro cultured plants and F3 generation flax plants overproducing the β-1,3-glucanase gene (EMO-βGlu flax) were characterized by up-regulation of β-glucanase and chitinase genes, decreases in the methylation of CCGG sequences in the β-glucanase gene and in total DNA methylation and, more importantly, reasonable resistance against Fusarium infection. In addition, EMO-βGlu flax obtained by this technology showed similar features as those obtained by genetic engineering.ConclusionTo our best knowledge, this is the first report on plant gene activation by treatment with oligodeoxynucleotides homologous to the coding region of the gene. Apart from the evident effectiveness, the most important issue is that the EMO method allows generation of favourably altered plants, whose cultivation makes the plant producer independent from the complicated procedure of obtaining an agreement on GMO release into the environment and whose products might be more easily introduced to the global market.Electronic supplementary materialThe online version of this article (doi:10.1186/s12870-014-0261-z) contains supplementary material, which is available to authorized users.

Highlights

  • Nowadays, the challenge for biotechnology is to develop tools for agriculture and industry to provide plants characterized by productivity and quality that will satisfy the growing demand for different kinds of natural products

  • Analysis of the expression of PR genes and PME1 The mRNA levels of selected PR proteins and pectin methylesterase 1 (PME1), another protein participating in the plant response to stress, were determined in the flax treated with OLIGOs and in the F3 generation of the selected line labelled epigenetically modified organisms (EMO)-βGlu

  • The analysis of the β-1,3-glucanases revealed enhanced expression of the first isoform in flax treated with four OLIGOs and increased expression of the second isoform in flax treated with OLIGOs B2 and B4 at 48 hours after exposure to OLIGOs

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Summary

Introduction

The challenge for biotechnology is to develop tools for agriculture and industry to provide plants characterized by productivity and quality that will satisfy the growing demand for different kinds of natural products. The substantial increase in the availability of genomic and biological data helps researchers and breeders to utilize biotechnological approaches to improve the productivity and quality ulcers, and micronized short fibres that appear to be suitable as a carrier and stabilizer of active substances (drugs, vitamins, hormones) [5,6,7]. In all these cases improved plant resistance against Fusarium has been detected [8]. The most dangerous pathogens of flax are: Fusarium oxysporum, which penetrates flax cell roots and spreads throughout the plant via the vascular system, leading to root rot and wilt of leaves, and Fusarium culmorum, which causes rot at the base of the shoots, resulting in progressive plant necrosis and in consequence plant death [9,10]

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