Abstract

Abstract False flax (Camelina sativa L.) is currently under-exploited but highly promising oilseed crop. Combining Camelina’s attractive agronomic traits with its unprecedented ease for genetic engineering makes it an ideal plant chassis for biotechnology applications, in particular synthetic biology strategies. For targeted expression of transgene particularly to seeds requires identification and application of seed specific promoters. In the present study two cultivars of Camelina, namely Zuzana and Smilowska, were used for transformation at early flowering stage using the floral dip method. The plants were inoculated with Agrobacterium bearing a construct for expression of red fluorescent protein (RFP) under the control of the seed specific cruciferin promoter CRUC from Arabidopsis. Transgenic seeds and plants were identified on the basis of red fluorescence (RFP) and kanamycin resistance. Relatively high transformation efficiency of 8 % was achieved particularly for the cultivar Zuzana. However, many of regenerants exerted developmental deformations such as lack of shoot apical meristem, deformed or absent cotyledons, etc. Furthermore, the activity of the CRUC promoter was still active also in true leaves rendering this promoter as inappropriate for seed targeting of the transgene. Nevertheless, genetic transformation remains a tool for direct modulation of pathways for oil synthesis in oilseed crops.

Highlights

  • Camelina sativa (L.), is an ancient crop of the Brassicaceae cultivated in Europe as an important oilseed crop for many centuries before it was displaced by higher-yielding crops, such as canola, soybean or sunflower

  • We show that the transformation of Camelina can be hampered, while potential reasons are discussed

  • Genetic transformation approach has been successful in achievement of the desirable Camelina traits, while specific promoters are important for seed-targeted modification to occur

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Summary

Introduction

Camelina sativa (L.), is an ancient crop of the Brassicaceae cultivated in Europe as an important oilseed crop for many centuries before it was displaced by higher-yielding crops, such as canola, soybean or sunflower. Intact transgenic Camelina plants can be obtained within 6 – 8 weeks (Lu and Kang 2008; Sitther et al 2018). Model organisms are being widely screened for identifying promoters that are tissueor developmental stage-specific to maximize the effect of transgene expression without affecting other tissues during growth and development (Jeong et al 2014; Polóniová et al 2015).

Results
Conclusion

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