Abstract

The CRISPR/Cas9 system is becoming an important genome editing tool for crop breeding. Although it has been demonstrated that target mutations can be transmitted to the next generation, their inheritance pattern has not yet been fully elucidated. Here, we describe the CRISPR/Cas9-mediated genome editing of four different rice genes with the help of online target-design tools. High-frequency mutagenesis and a large percentage of putative biallelic mutations were observed in T0 generations. Nonetheless, our results also indicate that the progeny genotypes of biallelic T0 lines are frequently difficult to predict and that the transmission of mutations largely does not conform to classical genetic laws, which suggests that the mutations in T0 transgenic rice are mainly somatic mutations. Next, we followed the inheritance pattern of T1 plants. Regardless of the presence of the CRISPR/Cas9 transgene, the mutations in T1 lines were stably transmitted to later generations, indicating a standard germline transmission pattern. Off-target effects were also evaluated, and our results indicate that with careful target selection, off-target mutations are rare in CRISPR/Cas9-mediated rice gene editing. Taken together, our results indicate the promising production of inheritable and “transgene clean” targeted genome-modified rice in the T1 generation using the CRISPR/Cas9 system.

Highlights

  • Creating the desired gene diversity in crop plants is the main goal of basic functional genomic research and molecular breeding in agriculture

  • Our results suggest that the inheritable and “transgene clean” targeted genome modification of rice in the T1 generation can be generated by the clustered regularly interspaced short palindromic repeat (CRISPR)/Cas[9] system

  • The absence of the transgene was determined to be concurrent in PCRs negative for Cas[9], sgRNA and hygromycin phosphotransferase (HPT) genes, and the results indicated that the T-DNA region could be segregated out in most lines

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Summary

Introduction

Creating the desired gene diversity in crop plants is the main goal of basic functional genomic research and molecular breeding in agriculture. Gene editing using engineering nucleases, e.g., zinc finger nuclease (ZFN) and transcription activator-like effector nuclease (TALEN), effectively generates genetic variants at specific sites in plant genomes. These nucleases induce site-specific double-strand breaks (DSBs) that are repaired, leading to genome modifications via homologous recombination (HR) or random deletion/insertion of a small DNA sequence adjacent to the target by non-homologous end-joining (NHEJ). There are limited studies indicating that the targeted genome modification created by CRISPR/Cas[9] can be transmitted in Arabidopsis, tobacco, tomato and rice[5,7,17,22,23,24,25,26,27]. Our results suggest that the inheritable and “transgene clean” targeted genome modification of rice in the T1 generation can be generated by the CRISPR/Cas[9] system

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