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Improving IscB to create tiny, efficient gene editing tools for animal cells and embryos
Updated
Abstract
An average 7.5-fold increase in activity was observed with engineered IscB proteins.
- Three substitutions in IscB proteins led to a significant increase in genome editing activity.
- The eIscB-D variant achieved a maximum editing efficiency of 91.3%.
- An engineered ωRNA was developed, resulting in a 20% reduction in length with improved efficiency.
- The eIscB-D/eωRNA system exhibited a 20.2-fold activity increase compared to original IscB.
- eIscB-D demonstrated high activity in mouse cell lines and embryos, facilitating disease model generation.
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