Submitted:
29 November 2023
Posted:
30 November 2023
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Abstract
Keywords:
Introduction
94% of Affected NGT Plants Would Enter the EU Market Without Risk Assessment
- (a)
- Consumption-oriented traits represent the largest group of intended traits (34 NGT1 plant applications), which covers for example traits affecting the nutrient content, visual and olfactory modifications or secondary metabolites of the crop. Examples for visual and olfactory modifications are non-browning fruits and vegetables.
- (b)
- The second largest trait group concerns industry-oriented traits (20 NGT1 plant applications) such as modified ingredient compositions, storage and transportability qualities, or bioenergy usage. Here, camelina plant applications with adapted fatty acid biosynthesis to produce biofuels or dietary supplements represent common examples.
- (c)
- The third group covers traits associated with plant development and cultivation (19 NGT1 plant applications), including plant growth, yield, reproduction and harvesting aspects. A plant application of this group is a “shatter-tolerant” NGT1 rapeseed developing more stable pods to prevent seed loss during harvesting.
- (d)
- The fourth trait group contains traits aiming to confer tolerance against biotic stressors such as bacteria, fungi, nematodes or viruses (13 NGT1 plant applications). An example is a wheat plant with fungal resistance due to a mutation affecting the plant immune response.
- (e)
- The fifth trait group includes herbicide resistances (7 NGT1 plant applications) that are mainly generated via point mutations in e.g. the ALS genes of soybean and rapeseed.
- (f)
- The least represented trait group covers abiotic stress tolerances (5 NGT1 plant applications) of which drought tolerance is a favored trait, which is proposed to confer adaptation to climate changes (Sami et al., 2021; Eckardt et al., 2023).
Intended traits and unintended risks
- (i)
- Persistence and invasiveness: Stress tolerance, both biotic and abiotic, that alters plant fitness may impact the plants persistence and establishment in the environment, even for crop plants that are so far not invasive and especially in changing climate regimes. NGT1 plant applications listed in Gelinsky (2022) comprise a potentially invasive tree tobacco, which showed an increased fitness after drought stress (Negin et al. 2023). Such a drought stress-tolerant tobacco could potentially grow in areas that previously had been too dry and thus might lead to risks for biodiversity in the corresponding ecosystems. In general, the risk of generating plants with increased persistence and invasiveness might be enhanced when wide-spread plants such as wild grasses, trees and herbs become targets of genetic modification as listed in the U.S. APHIS plant applications (Blackburn et al., 2019; Table S1). However, the EC proposal would not require any monitoring or detection concept for NGT1, which restricts risk management, including the capacity to remove invasive NGT plants to protect biodiversity.
- (ii)
- Gene transfer and selective disadvantages: The transfer of traits from domesticated plants to wild plant species can result in an altered weed spread as well as the establishment of novel weeds, which can lead to an increased risk for the extinction of wild species (Ellstrand, 2003). We identified a NGT1 rapeseed, which grows more stable pods to prevent seed loss during the harvesting process ('shatter-tolerance', Table S1). Unintended crossing of the ‘shatter-tolerant’ NGT1 rapeseed with wild plant populations could affect the fitness of wild plants and their natural reproduction due to possible restrictions in seed dispersal.
- (iii)
- Altering cultivation, management or harvesting techniques: GMO’s need to be analyzed in regards to their impact on the cultivation, management and harvesting techniques compared to non-GMO plants. This includes a potential increase in insecticide, herbicide, or pesticide usage. We identified non-browning fruits and vegetables that potentially harbor an effect on the cultivation system. The trait ‘non-browning’ often comprises a mutation in at least one of the polyphenol oxidase genes. Polyphenol oxidases are known to play a role in the plant pathogen defense, while their loss is associated with an impairment in biotic stress response (Thipyapong et al., 2004). A modification of the plant’s pathogen defense mechanism might change the plants susceptibility to biotic stress and therefore might alter the plant pest management by a potential increase in pesticide usage.
- (iv)
- Interactions with target and non-target organisms (NTOs): Environmental impacts resulting from direct and indirect interactions of GM plants with NTOs can also be identified for NGT plants. One example in which an interaction with NTOs cannot be excluded, is a patented NGT1 plant application. In this case a NGT1 plant would carry a genome edited microRNA (miRNA) conferring insecticidal activities in target (and potentially non-target) insects (see section “Within the realms of possibility: The NGT1-RNAi case”). In other cases, changes in metabolomics like in the protein or lipid content and composition as seen for many NGT1 plant applications in Gelinsky (2022), may also unintentionally affect the synthesis of byproducts and secondary metabolites potentially harmful to NTOs (Kawall, 2021).
Within the realms of possibility: The NGT1-RNAi case
Discussion
Supplementary Material
Author Contributions
Acknowledgments
Conflicts of Interest
References
- Arakane, Y., and Muthukrishnan, S. (2010). Insect chitinase and chitinase-like proteins. Cell Mol Life Sci 67, 201–216. [CrossRef]
- Blackburn, T. M., Bellard, C., and Ricciardi, A. (2019). Alien versus native species as drivers of recent extinctions. Frontiers in Ecol & Environ 17, 203–207. [CrossRef]
- Eckardt, N. A., Cutler, S., Juenger, T. E., Marshall-Colon, A., Udvardi, M., and Verslues, P. E. (2023). Focus on climate change and plant abiotic stress biology. Plant Cell 35, 1–3. [CrossRef]
- Eckerstorfer, M. F., Grabowski, M., Lener, M., Engelhard, M., Simon, S., Dolezel, M., et al. (2021). Biosafety of genome editing applications in plant breeding: Considerations for a focused case-specific risk assessment in the EU. BioTech 10. [CrossRef]
- Ellstrand, N. C. (2003). Dangerous liaisons? When cultivated plants mate with their wild relatives. Baltimore, Md. Johns Hopkins Univ. Press.
- European Commission (2013a). No 283/2013 of 1 March 2013 setting out the data requirements for active substances, in accordance with regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.
- European Commission (2013b). No 284/2013 of 1 March 2013 setting out the data requirements for plant protection products, in accordance with regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.
- European Court of Justice, Confédération paysanne. Judgement of the Court (Grand Chamber), 25 July 2018 in Case C-528/16. C-528-18.
- European Parliament, Council of the European Union (2001). Directive 2001/18/EC on the deliberate release into the environment of genetically modified organisms and repealing Council Directive 90/220/EEC: Directive 2001/18/EC.
- European Parliament, Council of the European Union (2009). No 1107/2009 concerning the placing of plant protection products on the market and repealing Council Directives 79/117/EEC and 91/414/EEC.
- European Parliament, Council of the European Union (2023a). Annexes of the proposal on plants obtained by certain new genomic techniques and their food and feed, and amending regulation (EU) 2017/625: COM(2023) 411 Annexes 1 to 3.
- European Parliament, Council of the European Union (2023b). Proposal for a regulation on plants obtained by certain new genomic techniques and their food and feed, and amending regulation (EU) 2017/625: COM(2023)411.
- Gelinsky, E. (2022). Neue gentechnische Verfahren: Kommerzialisierungspipeline im Bereich Pflanzenzüchtung und Lizenzvereinbarungen: Im Auftrag des Bundesamtes für Umwelt (BAFU). Baldegg.
- Hernández-Soto, A., and Chacón-Cerdas, R. (2021). RNAi Crop protection advances. Int J Mol Sci 22. [CrossRef]
- Kawall, K. (2021). Genome-edited Camelina sativa with a unique fatty acid content and its potential impact on ecosystems. Environ Sci Eur 33. [CrossRef]
- Khajuria, C., Buschman, L. L., Chen, M.-S., Muthukrishnan, S., and Zhu, K. Y. (2010). A gut-specific chitinase gene essential for regulation of chitin content of peritrophic matrix and growth of Ostrinia nubilalis larvae. Insect biochemistry and molecular biology 40. [CrossRef]
- Koch, A., and Wassenegger, M. (2021). Host-induced gene silencing - mechanisms and applications. New Phytol 231, 54–59. [CrossRef]
- Liu, S., Jaouannet, M., Dempsey, D. A., Imani, J., Coustau, C., and Kogel, K.-H. (2020). RNA-based technologies for insect control in plant production. Biotechnol Adv 39, 107463. [CrossRef]
- Lu, Q., Xie, H., Qu, M., Liu, T., and Yang, Q. (2023). Group h chitinase: A molecular target for the development of lepidopteran-specific Insecticides. J Agric Food Chem. [CrossRef]
- Maori, E., Galanty, Y., Pignocchi, C., Chaparro Garcia, A., and Meir, O. (2019). Modifying the specificity of plant non-coding RNA molecules for silencing gene expression. EP3684930. European Union: Tropic Biosciences UK Limited.
- Sami, A., Xue, Z., Tazein, S., Arshad, A., He Zhu, Z., Ping Chen, Y., et al. (2021). CRISPR-Cas9-based genetic engineering for crop improvement under drought stress. Bioengineered 12, 5814–5829. [CrossRef]
- Shabalina, S. A., and Koonin, E. V. (2008). Origins and evolution of eukaryotic RNA interference. Trends Ecol Evol 23, 578–587. [CrossRef]
- Song, X., Li, Y., Cao, X., and Qi, Y. (2019). MicroRNAs and their regulatory roles in plant-environment interactions. Annu Rev Plant Biol 70, 489–525. [CrossRef]
- Thipyapong, P., Hunt, M. D., and Steffens, J. C. (2004). Antisense downregulation of polyphenol oxidase results in enhanced disease susceptibility. Planta 220, 105–117. [CrossRef]
- Yu, Y., Jia, T., and Chen, X. (2017). The 'how' and 'where' of plant microRNAs. New Phytol 216, 1002–1017. [CrossRef]


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