About us
Research Centers
Key Laboratories
Recent Publications
International Cooperation
Education & Training
Join Us
Societies & Publications
  Location: Home >> Research >> Research Progress
Development of Prime Editing for Rice and Wheat
Many genetic and breeding studies have shown that point mutations and indels (insertions and deletions) can alter elite traits in crop plants{Zhao, 2011 #1561}. Although nuclease-initiated homology-directed repair (HDR) can generate such changes, it is limited by its low efficiency. Base editors are robust tools for creating base transitions but not transversions, insertions or deletions. Thus, there is a pressing need for new genome engineering approaches in plants.
David R. Liu and his co-workers at Harvard University developed a new genome editing approach, prime editing, which uses engineered Cas9 nickase (H840A)–reverse transcriptase (RT) fusion proteins paired with a prime editing guide RNA (pegRNA) that encodes the desired edit in human cells. The RT domain uses a nicked genomic DNA strand as a primer for the synthesis of an edited DNA flap templated by an extension on the pegRNA. Subsequent DNA repair incorporates the edited flap, permanently installing the programmed edit.
Recently, a research team led by Prof. GAO Caixia of the Institute of Genetics and Developmental Biology of the Chinese Academy of Sciences reported the optimization of a prime editing system (designated PPE system) for creating desired point mutations, insertions and deletions in two major cereal crops, namely, rice and wheat. The main components of a PPE system are a Cas9 nickase-reverse transcriptase (RT) fusion protein and a prime editing guide RNA (pegRNA).
Using the PPE system, these workers produced all 12 kinds of single base substitutions, as well as multiple point mutations and small DNA insertions and deletions at nine rice and seven wheat sites in protoplasts, with efficiencies up to 19.2%. The efficiency of PPE was strongly affected by the length of the primer binding site (PBS) and RT template. Although byproducts (off-target effects) were generated by the PPE system, these can be reduced by optimizing RT template length. Moreover, using a PPE system optimized for plants, they found that the original RT could be replaced by CaMV-RT (from Cauliflower mosaic virus) and retron-derived RT (from E. coli BL21). Prime editing efficiency was also improved at some targets by using their PPE-Ribozyme (PPE-R) and by incubating at 37℃.
Furthermore, GAO and her collaborators were able to create stable mutant rice plants carrying G-to-T point mutations, multi-nucleotide substitutions, and a number of desired 6-nt deletions, with a mutant production efficiency approaching 22%. It is noteworthy that these three types of mutation are very difficult to produce with current editing tools.
“Although the efficiency of the PPE system is lower than that of base editors, it is still an appealing new tool for creating all 12 types of single point mutation, mixtures of different substitutions, and insertions and deletions. The system thus has great potential for plant breeding and functional genomics research”, said Dr. GAO.
The scientific paper, entitled “Prime genome editing in rice and wheat”, was published in Nature Biotechnology (doi: 10.1038/s41587-020-0455-x, online at March 16, 2020). The research was supported by the National Natural Science Foundation of China, the Strategic Priority Research Program of the Chinese Academy of Sciences, the National Key Research and Development Program of China, and the U.S. NIH and HHMI.
Figure: The plant prime editing system (PPE) introduces desired edits in plants (a) Diagram of the PPE system. (b) BFP-to-GFP conversion frequencies of PPE systems measured by flow cytometry. (c) PPE systems install all 12 kinds of base substitution, as well as multiple base substitutions, insertions, and deletions into genomic sites. (Image by IGDB)
Mr. QI Lei
Institute of Genetics and Developmental Biology, Chinese Academy of Sciences