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Genome edited plants, without DNA 게시판 상세보기

Genome edited plants, without DNA- CRISPR-Cas9 RNP technique in plants could be the key to feeding the planet -

October 19, 2015

The public and scientists are at odds over the safety of genetically modified (GM) food. According to a January 2015 Pew Research Center report, only 37% of the public believe that GM foods are safe which is in stark contrast to the support from 88% of scientists. There is concern that adding DNA of different species will lead to unintended, undesirable consequences. Scientists at the IBS Center for Genome Engineering in South Korea have created a way to genetically modify plants using CRISPR-Cas9 without the addition of DNA. Because no DNA is used in this process, the resulting genome-edited plants could likely be exempt from current GMO regulations and given a warmer reception by the public.

What makes this work so groundbreaking is that these genetic modifications look just like genetic variations resulting from the selective breeding that farmers have been doing for millennia. IBS Director of the Center for Genome Engineering Jin-Soo Kim explains that “the targeted sites contained germline-transmissible small insertions or deletions that are indistinguishable from naturally occurring genetic variation.”


Figure 1. Schematic diagram of CRISPR-Cas9

CRISPR is an acronym for Clustered Regularly Interspaced Short Palindromic Repeat, which refers to the unique repeated DNA sequences found in bacteria and archaea. CRISPR is now used widely for genome editing. What’s crucial in genetic engineering is for the gene editing tool to be accurate and precise, which is where CRISPR-Cas9 excels. CRISPR-Cas9 uses a single guide RNA (sgRNA) to identify and edit the target gene and Cas9 (a protein) then cleaves the gene, resulting in site-specific DNA double-strand breaks (DSBs). When the cell repairs the DSB, the resulting fix is the intended genetic edit.

The beauty of this research is that the IBS research team has elevated the process and no longer uses DNA, being unshackled from GMO regulations. To do this, purified Cas9 protein was mixed with sgRNAs targeting specific genes from three plant species to form preassembled ribonucleoproteins (RNPs). The IBS team used these Cas9 RNPs to transfect several different plants including tobacco, lettuce and rice to achieve targeted mutagenesis in protoplasts. To test the efficacy of this process, the team delivered Cas9 RNPs to the protoplasts of the test plant species, and found Cas9 RNP-induced mutations 24 hours after transfection. These newly cloned lettuce cells showed no mosaicism which led the researchers to believe that the RGEN RNP may have cleaved the target site immediately after transfection and the indels occurred before cell division was completed.


Figure 1. Genetically customized lettuce made with CRISPR-Cas9

Finally, the team demonstrated that RGEN-induced mutations were maintained after regeneration. Using a Cas9 RNP, they disrupted a gene in lettuce called Brassinosteroid Insensitive 2 (BIN2) which regulates the signaling of brassinosteroid, a class of steroid hormones responsible for a wide range of physiological processes in the plant life cycle, including growth. They found that after cell division the lettuce cells maintained the disruption of the gene with a frequency of 46%. Importantly, there were no off-target indels. They grew full plants from the seeds of these genome edited and regenerated plants, which had the mutation from the previous generation. They were able to definitively show that Cas9 RNPs can be used to genetically modify plants, which Jin-Soo Kim points out, “paves the way for the widespread use of RNA-guided genome editing in plant biotechnology and agriculture.”

The IBS team’s technique of genome editing without inserting DNA could be revolutionary for the future of the seed industry. The RGEN RNP process will enable us to produce plants that are heartier and more suited to climate change in order to feed Earth’s increasing population. Currently European Union GMO regulations don’t allow for food with added DNA. Since the Cas9 RNP technique does not use DNA, it may be able to avoid being in violation of these rules. In addition, using Cas9 RNP is cheaper, faster and more accurate to apply to plants than previous breeding techniques (like radiation-induced mutations). Large agribusiness companies have been able to afford the time and money necessary to create seeds for genetically modified food, but the Cas9 RNP technique could allow for a more decentralized gene-edited seed production industry.

This process is ready for use to bolster plant output and create heartier crops in foods like tomatoes and lettuce. The application of the Cas9 RNP gene editing technique could be the next step in ending food shortages.

By Daniel Kopperud

Notes for editors

- References
Je Wook Woo, Jungeun Kim, Soon Il Kwon, Claudia Corvalán, Seung Woo Cho, Hyeran Kim, Sang-Gyu Kim, Sang-Tae Kim, Sunghwa Choe & Jin-Soo Kim; Nature Biotechnology, DOI: 10.1038/nbt.3389

- Media Contact
For further information or to request media assistance, please contact: Mr. Shi Bo Shim, Head of Department of Communications, Institute for Basic Science (+82-42-878-8189; sibo@ibs.re.kr) or Ms. Carol Kim, Department of Communications, Institute for Basic Science (+82-42-878-8133; clitie620@ibs.re.kr)

- About the Institute for Basic Science (IBS)
IBS was founded in 2011 by the government of the Republic of Korea with the sole purpose of driving forward the development of basic science in Korea It comprises a total of 50 research centers in all fields of basic science, including mathematics, physics, chemistry, life science, earth science and interdisciplinary science. IBS has launched 25 research centers as of October 2015.There are eight physics, one mathematics, six chemistry, eight life science, and two interdisciplinary research centers.

 

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