Discovery of diverse DNA cytosine deaminases enables a single-enzyme method for base resolution methylation detection
Ontology highlight
ABSTRACT:
PROVIDER: PRJNA978603 | ENA |
REPOSITORIES: ENA
Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| SRR24798417_1.fastq.gz | Fastqsanger.gz | |||
| SRR24798417_2.fastq.gz | Fastqsanger.gz | |||
| SRR24798418_1.fastq.gz | Fastqsanger.gz | |||
| SRR24798418_2.fastq.gz | Fastqsanger.gz | |||
| SRR24798419_1.fastq.gz | Fastqsanger.gz |
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Project description:Base editors are RNA-guided deaminases that enable site-specific nucleotide transitions. The targeting scope of these Cas-deaminase fusion proteins critically depends on the availability of a protospacer adjacent motif (PAM) at the selected genomic locus, and is limited to a window within the CRISPR-Cas R-loop where single stranded (ss)DNA is accessible to the deaminase. Here, we reason that the Cas9-HNH nuclease domain sterically constrains ssDNA accessibility, and demonstrate that omission of this domain expands the editing window. By exchanging the HNH nuclease domain with an adenosine deaminase, we furthermore engineer adenine base editor variants (HNHx-ABE) with PAM-proximally shifted editing windows. HNHx-ABEs are substantially reduced in size, and expand the targeting scope of base editors. Our finding that the HNH domain is replaceable could moreover benefit future protein engineering efforts, where Cas9 operates together with other enzyme domains.
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