Nature Communications (Jul 2024)

Dual activities of an X-family DNA polymerase regulate CRISPR-induced insertional mutagenesis across species

  • Trevor Weiss,
  • Jitesh Kumar,
  • Chuan Chen,
  • Shengsong Guo,
  • Oliver Schlegel,
  • John Lutterman,
  • Kun Ling,
  • Feng Zhang

DOI
https://doi.org/10.1038/s41467-024-50676-4
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 12

Abstract

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Abstract The canonical non-homologous end joining (c-NHEJ) repair pathway, generally viewed as stochastic, has recently been shown to produce predictable outcomes in CRISPR-Cas9 mutagenesis. This predictability, mainly in 1-bp insertions and small deletions, has led to the development of in-silico prediction programs for various animal species. However, the predictability of CRISPR-induced mutation profiles across species remained elusive. Comparing CRISPR-Cas9 repair outcomes between human and plant species reveals significant differences in 1-bp insertion profiles. The high predictability observed in human cells links to the template-dependent activity of human Polλ. Yet plant Polλ exhibits dual activities, generating 1-bp insertions through both templated and non-templated manners. Polλ knockout in plants leads to deletion-only mutations, while its overexpression enhances 1-bp insertion rates. Two conserved motifs are identified to modulate plant Polλ‘s dual activities. These findings unveil the mechanism behind species-specific CRISPR-Cas9-induced insertion profiles and offer strategies for predictable, precise genome editing through c-NHEJ.