Regulation of gene editing using T-DNA concatenation

Nat Plants. 2023 Sep;9(9):1398-1408. doi: 10.1038/s41477-023-01495-w. Epub 2023 Aug 31.

Abstract

Transformation via Agrobacterium tumefaciens is the predominant method used to introduce exogenous DNA into plant genomes1,2. Transfer DNA (T-DNA) originating from Agrobacterium can be integrated as a single copy or in complex concatenated forms3,4, but the mechanisms affecting final T-DNA structure remain unknown. Here we demonstrate that inclusion of retrotransposon (RT)-derived sequences in T-DNA can increase T-DNA copy number by more than 50-fold in Arabidopsis thaliana. These additional T-DNA copies are organized into large concatemers, an effect primarily induced by the long terminal repeats (LTRs) of RTs that can be replicated using non-LTR DNA repeats. We found that T-DNA concatenation is dependent on the activity of the DNA repair proteins MRE11, RAD17 and ATR. Finally, we show that T-DNA concatenation can be used to increase the frequency of targeted mutagenesis and gene targeting. Overall, this work uncovers molecular determinants that modulate T-DNA copy number in Arabidopsis and demonstrates the utility of inducing T-DNA concatenation for plant gene editing.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Arabidopsis* / genetics
  • Gene Editing*
  • Genes, Plant
  • Genome, Plant
  • Retroelements / genetics

Substances

  • T-DNA
  • Retroelements