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Abstract
PARP1 downregulation increased both NHEJ and MMEJ repair activities.
- Non-homologous end joining (NHEJ) often leads to mutagenic repair through insertions or deletions.
- Microhomology-mediated end joining (MMEJ) results in larger deletions due to end resection.
- Homologous recombination (HR) allows for precise sequence changes but is typically inefficient in many cell types.
- PARP1 downregulation did not affect HR while enhancing both NHEJ and MMEJ repair pathways.
- PARP1 overexpression reduced NHEJ and HR activity but did not impact MMEJ.
- Targeted modulation of PARP1 is associated with potential improvements in the precision of CRISPR-based genome editing.
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