2023
DOI: 10.3389/fgeed.2023.1074641
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Editing efficiencies with Cas9 orthologs, Cas12a endonucleases, and temperature in rice

Abstract: The advent of CRISPR-Cas technology has made it the genome editing tool of choice in all kingdoms of life, including plants, which can have large, highly duplicated genomes. As a result, finding adequate target sequences that meet the specificities of a given Cas nuclease on any gene of interest remains challenging in many cases. To assess target site flexibility, we tested five different Cas9/Cas12a endonucleases (SpCas9, SaCas9, St1Cas9, Mb3Cas12a, and AsCas12a) in embryogenic rice calli from Taipei 309 at 3… Show more

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Cited by 3 publications
(2 citation statements)
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“…The next level is epigenetic editors that do not change the genome sequence and affect the activity of genes at the levels of their transcription, splicing and translation [318]. SpCas9 orthologues from other bacteria are also used, as well as CRISPR/Cas systems of other types [319]. A second frequently used edit is Cas12a [320], a smaller protein that has only one nuclease domain and, therefore, leaves sticky rather than blunt ends.…”
Section: Development Of Sustainable Geneticallymentioning
confidence: 99%
“…The next level is epigenetic editors that do not change the genome sequence and affect the activity of genes at the levels of their transcription, splicing and translation [318]. SpCas9 orthologues from other bacteria are also used, as well as CRISPR/Cas systems of other types [319]. A second frequently used edit is Cas12a [320], a smaller protein that has only one nuclease domain and, therefore, leaves sticky rather than blunt ends.…”
Section: Development Of Sustainable Geneticallymentioning
confidence: 99%
“…As gene knockout technology matures, CRISPR-Cas9 genome editing has rapidly become an important tool in genomic research [19,20]. During the repair process, mismatching via base insertion or deletion usually occurs, resulting in code-shifting mutations.…”
Section: Of 13mentioning
confidence: 99%