Abstract
Evolved xCas9(3.7) variant with broad PAM compatibility has been reported in cell lines, while its editing efficiency was site-specific. Here, we show that xCas9(3.7) can recognize a broad PAMs including NGG, NGA, and NGT, in both embryos and Founder (F0) rabbits. Furthermore, the codon-optimized xCas9-derived base editors, exBE4 and exABE, can dramatically improve the base editing efficiencies in rabbit embryos. Our results demonstrated that the optimized xCas9 with expanded PAM compatibility and enhanced base editing efficiency could be used for precise gene modifications in organisms.
Keywords:
Base editors; CRISPR; PAM compatibility; xCas9.
MeSH terms
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Animals
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Animals, Genetically Modified
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CRISPR-Associated Protein 9 / genetics*
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CRISPR-Associated Protein 9 / metabolism
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CRISPR-Cas Systems*
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Codon
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Dystrophin / genetics
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Dystrophin / metabolism
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Embryo, Mammalian
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Founder Effect*
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Gene Editing / methods*
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Gene Expression
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Gene Targeting / methods*
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High-Throughput Nucleotide Sequencing
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Microinjections
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Plasmids / chemistry
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Plasmids / metabolism
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Poly(A)-Binding Proteins / genetics
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Poly(A)-Binding Proteins / metabolism
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Presenilin-1 / genetics
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Presenilin-1 / metabolism
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RNA, Guide, CRISPR-Cas Systems / genetics*
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RNA, Guide, CRISPR-Cas Systems / metabolism
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Rabbits
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Trinucleotide Repeats
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Zygote
Substances
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Codon
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Dystrophin
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Poly(A)-Binding Proteins
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Presenilin-1
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RNA, Guide, CRISPR-Cas Systems
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CRISPR-Associated Protein 9