CRISPR/dCas13(Rx) Derived RNA N<sup>6</sup>-methyladenosine (m<sup>6</sup>A) Dynamic Modification in Plant.
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ABSTRACT: N6-methyladenosine (m6A) is the most prevalent internal modification of mRNA and plays an important role in regulating plant growth. However, there is still a lack of effective tools to precisely modify m6A sites of individual transcripts in plants. Here, programmable m6A editing tools are developed by combining CRISPR/dCas13(Rx) with the methyltransferase GhMTA (Targeted RNA Methylation Editor, TME) or the demethyltransferase GhALKBH10 (Targeted RNA Demethylation Editor, TDE). These editors enable efficient deposition or removal of m6A modifications at targeted sites of endo-transcripts GhECA1 and GhDi19 within a broad editing window ranging from 0 to 46 nt. TDE editor significantly decreases m6A levels by 24%-76%, while th
SUBMITTER: Yu L
PROVIDER: S-EPMC11497087 | biostudies-literature | 2024 Oct
REPOSITORIES: biostudies-literature
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