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Beyond Crispr:Single Base Editors for Human Health and Crop Improvement
During 2016–2018, CRISPR/Cas9 technology was modified using disabled Cas9 with nickase activity in combination with cytosine/adenine deaminases for the development of four generations of cytosine base editors (BE1–BE4) for C → U conversion and at least seven generations of adenine base editors (ABE1–ABE7) for A → I conversion. These base editors exhibited improved efficiency and reduced frequency of deletions among the products. Further improvement in the form of enhanced base editors and high-fidelity base editors was achieved through the use of 1-3 copies of uracil N-glycosylase inhibitors and phage Mu-Gam protein. The technology will bring precision to gene editing technology for human healthcare and crop improvement.
Keywords
AID/APOBEC, Base Editing, CRISPR/Cas9, Cytidine/Adenine Deaminases, Target AID.
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