Page 60 - Plant Canada 2024 Proceeding
P. 60

PLANT CANADA 2024


                                                     Monday, July 8

                                                     Dr. Dan Voytas
                                                     University of Minnesota

                                                     “Overcoming Bottlenecks in Plant Gene Editing”

                                                     Abstract: Plant gene editing is usually carried out
                                                     by delivering reagents such as Cas9 and sgRNAs to
                                                     explants in culture. Edited cells are then induced to
                                                     differentiate into whole plants by exposure to
                                                     various hormones. Creating edited plants through
                                                     tissue culture is often inefficient, requires
                                                     considerable time, only works with limited species
                                                     and genotypes and causes unintended changes to
                                                     the genome and epigenome. We have been
                                                     pursuing alternative approaches for plant gene
                                                     editing that minimize or obviate the need for tissue
               culture. In one approach, we generate gene edited dicotyledonous plants through de
               novo meristem induction. Developmental regulators and gene editing reagents are
               delivered to somatic cells on whole plants. Meristems are induced that produce shoots
               with targeted DNA modifications, and gene edits are transmitted to the next generation.
               In a second approach, we use RNA viruses to deliver sgRNAs through infection to
               transgenic plants that express Cas9. The sgRNAs are augmented with sequences that
               promote cell-to-cell mobility and movement into the meristem. Gene edited shoots are
               thus generated that transmit gene edits to the next generation. Because both
               approaches minimize the need for tissue culture, they promise to help overcome this
               bottleneck in plant gene-editing.

               Bio:  Dr. Dan Voytas is a Professor in the Department of Genetics, Cell Biology and
               Development and the Director of the Center for Precision Plant Genomics at the University of
               Minnesota. Dr. Voytas graduated from Harvard College in 1984 and received his Ph.D. from
               Harvard Medical School in 1990. He conducted postdoctoral research at Johns Hopkins
               University School of Medicine. Prior to joining the University of Minnesota in 2008, Dr. Voytas
               was a professor at Iowa State University. Dr. Voytas’ research focuses on developing methods
               to edit plant genomes. Dr. Voytas’ lab is currently optimizing methods for efficiently making
               targeted genome modifications in a variety of plant species to advance basic biology and
               develop new crop varieties. In addition to his position at the University of Minnesota, Dr. Voytas
               co-founded Calyxt, an agricultural biotechnology company that used gene editing for crop
               improvement. In 2019, Dr. Voytas was elected to the National Academy of Sciences.












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