AcMYB10 Involved in Anthocyanin Regulation of ‘Hongyang’ Kiwifruit Induced via Fruit Bagging and High-Postharvest-Temperature Treatments

Author:

Yu Min1,Xiong Jinyu2,Dong Kun3,Quan Xin2,Guo Hao2,Huo Junwei24,Qin Dong24,Wang Yanchang5,Lu Xuemei5,Zhu Chenqiao24

Affiliation:

1. College of Life Science, Northeast Agricultural University, Harbin 150030, China

2. College of Horticulture & Landscape Architecture, Northeast Agricultural University, Harbin 150030, China

3. Horticulture Branch, Heilongjiang Academy of Agricultural Sciences, Harbin 150040, China

4. Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (Northeast Region), Ministry of Agriculture and Rural Affairs, Harbin 150030, China

5. Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan 430074, China

Abstract

Light and temperature are key factors influencing the accumulation of anthocyanin in fruit crops. To assess the effects of fruit bagging during development and high post-ripening temperature on ‘Hongyang’ kiwifruit, we compared the pigmentation phenotypes and expression levels of anthocyanin-related genes between bagged and unbagged treatments, and between 25 °C and 37 °C postharvest storage temperatures. Both the bagging and 25 °C treatments showed better pigmentation phenotypes with higher anthocyanin concentrations. The results of the qRT-PCR analysis revealed that the gene expression levels of LDOX (leucoanthocyanidin dioxygenase), F3GT (UDP-flavonoid 3-O-glycosyltransferase ), AcMYB10, and AcbHLH42 were strongly correlated and upregulated by both the bagging treatment and 25 °C storage. The results of bimolecular fluorescence complementation and luciferase complementation imaging assays indicated an interaction between AcMYB10 and AcbHLH42 in plant cells, whereas the results of a yeast one-hybrid assay further demonstrated that AcMYB10 activated the promoters of AcLODX and AcF3GT. These results strongly suggest that enhanced anthocyanin synthesis is caused by the promoted expression of AcLODX and AcF3GT, regulated by the complex formed by AcMYB10–AcbHLH42.

Funder

National Key R&D Program of China

Heilongjiang Postdoctoral Science Foundation

Young Talents Foundation of NEAU

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

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