# Transgene-free genome editing in citrus and poplar trees using positive and negative selection markers

**Authors:** Dhiôvanna Corrêia Rocha, Miracle Osazee Omoregbee, Danyel Fernandes Contiliani, Rushil Mandlik, Gen Li, Juliet Mascoveto, Gary Coleman, James N. Culver, Daniel Rodriguez Leal, Alessandra Alves de Souza, Yiping Qi

PMC · DOI: 10.1007/s00299-025-03627-2 · 2025-10-22

## TL;DR

Researchers developed a method to edit the genomes of citrus and poplar trees without leaving transgenes, using a base editor and selection markers.

## Contribution

A novel co-editing strategy using a cytosine base editor and selection markers enables transgene-free genome editing in perennial plants.

## Key findings

- The CBE-based co-editing strategy successfully edited citrus and poplar plants, though with low efficiency for biallelic edits.
- The addition of TLS mobile RNA unexpectedly reduced genome editing efficiency in both transgenic and non-transgenic plants.
- A small fraction of transgene-free plants survived selection, demonstrating a promising approach for transgene-free genome editing.

## Abstract

Transgene-free genome editing of the gene of interest in citrus and poplar has been achieved by co-editing the ALS gene via transient transgene expression of an efficient cytosine base editor.

CRISPR-Cas genome editing systems have been widely used in plants. However, such genome-edited plants are nearly always transgenic in the first generation when Agrobacterium-mediated transformation is used. Transgene-free genome-edited plants are valuable for genetic analysis and breeding as well as simplifying regulatory approval. It can be challenging to generate transgene-free genome-edited plants in vegetatively propagated or perennial plants. To advance transgene-free genome editing in citrus and poplar, we investigated a co-editing strategy using an efficient cytosine base editor (CBE) to edit the ALS gene to confer herbicide resistance combined with transient transgene expression and potential mobile RNA-based movement of CBE transcripts to neighboring, non-transgenic cells. An FCY-UPP based cytotoxin system was used to select non-transgenic plants that survive after culturing on 5-FC containing medium. While the editing efficiency is higher in poplar than in citrus, our results show that the CBE-based co-editing strategy works in both citrus and poplar, albeit with low efficiency for biallelic edits. Unexpectedly, the addition of the TLS mobile RNA sequence reduced genome editing efficiency in both transgenic and non-transgenic plants. Although a small fraction of escaping plants is detected in both positive and negative selection processes, our data demonstrate a promising approach for generating transgene-free base-edited plants.

The online version contains supplementary material available at 10.1007/s00299-025-03627-2.

## Linked entities

- **Genes:** IGFALS (insulin like growth factor binding protein acid labile subunit) [NCBI Gene 3483], UPP1 (uridine phosphorylase 1) [NCBI Gene 7378], FUS (FUS RNA binding protein) [NCBI Gene 2521]
- **Chemicals:** 5-FC (PubChem CID 3366)
- **Species:** Citrus (taxon 2706)

## Full-text entities

- **Genes:** SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}
- **Chemicals:** FCY (-), cytosine (MESH:D003596), 5-FC (MESH:D005437)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12546424/full.md

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Source: https://tomesphere.com/paper/PMC12546424