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Transcription activator-like effector(TALE) nucleases(TALENs) are increasingly used as a powerful tool for genome editing in a variety of organisms. We have previously cloned the TALE-coding gene avr Xa23 from Xanthomonas oryzae pv. oryzae and developed an Avr Xa23-based assembly system for designer TALEs or TALENs. Here,we exploit TALENs to induce mutagenesis of the rice ethylene response factor(ERF) transcription factor Os ERF922 for testing the gene-editing efficiency of Avr Xa23-based TALENs system. A pair of TALENs(T-KJ9/KJ10) was assembled and their nuclease activities were first confirmed in rice protoplast transient assay. The TALENs-expressing construct p T-KJ9/KJ10 was then used for rice transformation. We observed targeting somatic mutagenesis frequency of 15.0% in positive transgenic rice calli and obtained two mutant plants with nucleotide deletion or insertion at the designer target region. Our work demonstrates that the Avr Xa23-based TALENs system can be used for site-specific genome editing in rice.
We have previously cloned the TALE-coding gene avr Xa23 from Xanthomonas oryzae pv. Oryzae and developed an Avr Xa23 (TALENs) are increasingly used as a powerful tool for genome editing in a variety of organisms. -based assembly system for designer TALEs or TALENs. Here, we exploit TALENs to induce mutagenesis of the rice ethylene response factor (ERF) transcription factor Os ERF922 for testing the gene-editing efficiency of Avr Xa23-based TALENs system. A pair of TALENs (T-KJ9 / KJ10) was assembled and their nuleaselease activities were first confirmed in rice protoplast transient assay. The TALENs-expressing construct p T-KJ9 / KJ10 was then used for rice transformation. We observed targeting somatic mutagenesis frequency of 15.0% in positive transgenic rice calli and obtained two mutant plants with nucleotide deletion or insertion at the designer target region. Our work demonstrates that the Avr Xa23-based TALENs system can be used for site-s pecific genome editing in rice.