Cas9-induced nonhomologous recombination in C. elegans .
Stefan ZdraljevicLeonid KruglyakHeriberto MarquezLeonid KruglyakPublished in: bioRxiv : the preprint server for biology (2023)
Identification of the genetic basis of phenotypic variation within species remains challenging. In species with low recombination rates, such as Caenorhabditis elegans , genomic regions linked to a phenotype of interest by genetic mapping studies are often large, making it difficult to identify the specific genes and DNA sequence variants that underlie phenotypic differences. Here, we introduce a method that enables researchers to induce targeted recombination in C. elegans with Cas9. We demonstrate that high rates of targeted recombination can be induced by Cas9 in a genomic region in which naturally occurring recombination events are exceedingly rare. We anticipate that Cas9-induced nonhomologous recombination (CINR) will greatly facilitate high-resolution genetic mapping in this species.
Keyphrases
- dna repair
- dna damage
- crispr cas
- high resolution
- copy number
- genome editing
- genome wide
- high glucose
- diabetic rats
- cancer therapy
- dna methylation
- drug induced
- circulating tumor
- mass spectrometry
- bioinformatics analysis
- endothelial cells
- transcription factor
- circulating tumor cells
- tandem mass spectrometry
- genome wide identification