CRISPR/Cas9-Mediated Mutagenesis of MdCNGC2 in Apple Callus and VIGS-Mediated Silencing of MdCNGC2 in Fruits Improve Resistance to Botryosphaeria dothidea

Huijuan Zhou; Suhua Bai; Nan Wang; Xiaohong Sun; Yugang Zhang; Jun Zhu; Chaohua Dong

doi:10.3389/fpls.2020.575477

CRISPR/Cas9-Mediated Mutagenesis of MdCNGC2 in Apple Callus and VIGS-Mediated Silencing of MdCNGC2 in Fruits Improve Resistance to Botryosphaeria dothidea

Front Plant Sci. 2020 Nov 9:11:575477. doi: 10.3389/fpls.2020.575477. eCollection 2020.

Authors

Huijuan Zhou^{1

2

3}, Suhua Bai^{1

2

3}, Nan Wang^{1

2

3}, Xiaohong Sun^{1

2}, Yugang Zhang^{2

4}, Jun Zhu^{2

4}, Chaohua Dong^{1

2

3}

Affiliations

¹ Key Laboratory of Plant Biotechnology of Shandong Province, College of Life Sciences, Qingdao Agricultural University, Qingdao, China.
² Qingdao Key Laboratory of Genetic Improvement and Breeding in Horticultural Plants, Qingdao Agricultural University, Qingdao, China.
³ Shandong Province Key Laboratory of Applied Mycology, Qingdao, China.
⁴ College of Horticulture, Qingdao Agricultural University, Qingdao, China.

Abstract

Cyclic nucleotide-gated ion channels (CNGCs) have been reported to be involved in multiple plant physiological processes. Their involvement in plant immunity has been studied in several herbal plant species. It remains unclear whether CNGCs in woody plants play a similar role in plant immunity. In the present study, we identified an apple CNGC (designated as MdCNGC2), which is the homolog of Arabidopsis CNGC2. Analysis of tissue distribution revealed that MdCNGC2 was expressed in all tested tissues. Abundant transcripts of MdCNGC2 were observed in leaves and shoot bark. Low expression was observed in fruits and roots. MdCNGC2 expression was induced in apple callus and shoot bark by Botryosphaeria dothidea. The induction of MdCNGC2 was significantly higher in susceptible cultivars "Fuji," "Ralls Janet," and "Gala" compared to the resistant cultivar "Jiguan," suggesting that MdCNGC2 may be a negative regulator of resistance to B. dothidea. MdCNGC2 mutagenesis mediated by gene editing based on the CRISPR/Cas9 system led to constitutive accumulation of SA in apple callus. A culture filtrate of B. dothidea (BCF) induced the expression of several defense-related genes including MdPR1, MdPR2, MdPR4, MdPR5, MdPR8, and MdPR10a. Moreover, the induction of these genes was significantly higher in mdcngc2 mutant (MUT) callus than in wild type (WT) callus. Further analysis showed that the spread of B. dothidea was significantly lower on MUT callus than on WT callus. Knockdown of the MdCNGC2 gene reduced lesions caused by B. dothidea in apple fruits. These results collectively indicate that MdCNGC2 is a negative regulator of resistance to B. dothidea in apple callus.

Keywords: Botryosphaeria dothidea; Malus domestica; apple callus; gene editing; immune defense.