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Novel technologies to enhance breeding objectives and improve disease management strategies Dr. Ewen Mullins Teagasc Horticultural Technologies Seminar Ashtown, May 4th, 2017 Generating novel varieties - traditional breeding High value variety A Short stem + low dis. res. 2 Teagasc Presentation Footer x. Variety B Long stem + high dis. res. Generating novel varieties - traditional breeding But availability of parental material with high value traits can be limiting What can you do if parental material is not adequate? In 1940s discovered chemical and physical mutagens can modify the genetic code of existing material to produce plants possessing novel traits 3 Teagasc Presentation Footer Generating novel varieties - mutation breeding Using X-rays, nuclear radiation, chemical mutagens >3200 varieties generated across >200 plant species Clearfield™ oilseed rape, Ruby Red™, Golden Promise malting barley, Japanese pear, legumes, rice… BUT…. No EU regulation No control over what genes are mutated Very large populations (>10,000s) of mutant lines have to be screened to identify ‘upgraded’ plant Now, proteins can be used to mutate/edit specific genes Generating novel varieties - genome editing These proteins (termed CRISPR) are directed via a ‘satnav’ component Traditional Genome Editing Mutagenesis Breeding Act as a ‘molecular scissors’ to snip the genetic code. Generating novel varieties - genome editing Genome editing is faster and more precise and can be used to ‘upgrade’ welladapted varieties For example; powdery mildew resistance in bread wheat (Wang et al. 2014) Teagasc currently investigating potential of genome editing on barley, wheat, potato No regulatory restrictions on use of editing proteins for mutation breeding 7 8 Teagasc Presentation Footer • Barley, maize, rice, sorghum, soybean, potato, wheat • Circumvent years/decades of breeding to develop enhanced traits in existing varieties Mushrooms leading the way… “The long-awaited decision means that the edited mushroom can be cultivated and sold without passing through the USDA’s regulatory process — making it the first CRISPR-edited organism to receive a green light from the US government”. 9 Teagasc Presentation Footer To conclude… Mutation breeding since 1940s Gene editing more efficient form of mutation breeding Mutation breeding v. 2.0 Gene editing technologies are mainstream in research programmes Gene editing ≠ GM Irish, English, German, Dutch and Swedish regulatory agencies have stated edited varieties fall outside the EU legislation Currently no regulations required Future regulations ? Brexit ? 11 Teagasc Presentation Footer Thank you 12 Teagasc Presentation Footer