Abstract

Although the CRISPR/Cas9 system has been widely used for crop breeding, its application for the genetic improvement of trees has been limited, partly because of the outcrossing nature and substantial genomic heterozygosity of trees. Shanxin yang (Populus davidiana × P. bolleana), is a commercially important poplar clone that is widely grown in northern China. An established transformation protocol for this interspecific hybrid enables researchers to simultaneously investigate the efficiency and specificity of the CRISPR/Cas9-mediated manipulation of a highly heterozygous genome. Using the phytoene desaturase gene (PDS) as an example, we revealed that the CRISPR/Cas9 system could efficiently edit the Shanxin yang genome. Two sgRNAs were designed and incorporated into a single binary vector containing the Cas9 expression cassette. Among 62 independent transgenic lines, 85.5% exhibited an exclusively albino phenotype, revealing the total loss of PDS function. The Illumina sequencing results confirmed the targeted mutation of PdbPDS homologs induced by CRISPR/Cas9, and small insertions/deletions were the most common mutations. Biallelic and homozygous knockout mutations were detected at both target sites of the T0 transformants. Off-target activity was detected for sgRNA2 with a frequency of 3.2%. Additionally, the SNP interference of targeting specificity was assessed based on the sequence variation among PdbPDS homologs. A single mismatch at 19- or 10-bp from the PAM was tolerated by the CRISPR/Cas9 system. Therefore, multiple homologous genes were simultaneously edited despite the presence of a mismatch between the sgRNA and the target site. The establishment of a viable CRISPR/Cas9-based strategy for editing the Shanxin yang genome will not only accelerate the breeding process, but may also be relevant for other economically or scientifically important non-model plants species.

Highlights

  • The CRISPR/Cas9 system is a revolutionary technology for plant breeding because of its simplicity, efficiency, and versatility (Bortesi and Fischer, 2015; Gao, 2018)

  • A sequence alignment revealed that the longer product included two SNPcontaining allelic fragments (PdbPDS1-1 and PdbPDS1-2), which showed a higher similarity with Potri.014G148700 (Figure 1C)

  • The shorter product comprised only one amplicon (PdbPDS2), which displayed a higher identity with Potri.002G235200

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Summary

Introduction

The CRISPR/Cas system is a revolutionary technology for plant breeding because of its simplicity, efficiency, and versatility (Bortesi and Fischer, 2015; Gao, 2018). This system consists of two essential components, the Cas nuclease and a single guide RNA (sgRNA), which can induce double-strand breaks at specific genomic sites (Jinek et al, 2012). Recalcitrance to transformation and/or difficulties in regeneration are two predominant issues preventing the more widespread application of CRISPR in woody plants (Bewg et al, 2018) Their outcrossing nature and highly heterozygous genomes represent additional challenges to the genetic editing of tree species. In Populus species, one SNP altering the protospacer adjacent motif (PAM) site from NGG to NGA insulated the genome completely from editing (Zhou et al, 2015)

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