AcHZP45 is a repressor of chlorophyll biosynthesis and activator of chlorophyll degradation in kiwifruit

Author:

Wu Ying-ying1,Wang Ling-li23,Lin Yi-lai1,Li Xiang4,Liu Xiao-fen1,Xu Zi-Hong23,Fu Bei-ling1,Wang Wen-qiu1ORCID,Allan Andrew C56ORCID,Tu Mei-yan23,Yin Xue-ren1ORCID

Affiliation:

1. Horticulture Department, College of Agriculture and Biotechnology, Zhejiang University , Hangzhou 310058 , China

2. Horticulture Research Institute, Sichuan Academy of Agricultural Sciences , Chengdu 610066 , China

3. Key Laboratory of Horticultural Crop Biology and Germplasm Creation in Southwestern China, Ministry of Agriculture and Rural Affairs , Chengdu 610066 , China

4. School of Horticulture, Anhui Agricultural University , Hefei 230036 , China

5. The New Zealand Institute for Plant & Food Research Limited (Plant & Food Research) Mt Albert , Private Bag 92169, Auckland 1142 , New Zealand

6. School of Biological Sciences, University of Auckland , Private Bag 92019, Auckland 1142 , New Zealand

Abstract

Abstract The degradation of chlorophyll during fruit development is essential to reveal a more ‘ripe’ color that signals readiness to wild dispersers of seeds and the human consumer. Here, comparative biochemical analysis of developing fruit of Actinidia deliciosa cv. Xuxiang (‘XX’, green-fleshed) and Actinidia chinensis cv. Jinshi No.1 (‘JS’, yellow-fleshed) indicated that variation in chlorophyll content is the major contributor to differences in flesh color. Four differentially expressed candidate genes were identified: the down-regulated genes AcCRD1 and AcPOR1 involved in chlorophyll biosynthesis, and the up-regulated genes AcSGR1 and AcSGR2 driving chlorophyll degradation. Prochlorophyllide and chlorophyllide, the metabolites produced by AcCRD1 and AcPOR1, progressively reduced in ‘JS’, but not in ‘XX’, indicating that chlorophyll biosynthesis was less active in yellow-fleshed fruit. AcSGR1 and AcSGR2 were verified to be involved in chlorophyll degradation, using both transient expression in tobacco and stable overexpression in kiwifruit. Furthermore, a homeobox-leucine zipper (HD-Zip II), AcHZP45, showed significantly increased expression during ‘JS’ fruit ripening, which led to both repressed expression of AcCRD1 and AcPOR1 and activated expression of AcSGR1 and AcSGR2. Collectively, the present study indicated that different dynamics of chlorophyll biosynthesis and degradation coordinate the changes in chlorophyll content in kiwifruit flesh, which are orchestrated by the key transcription factor AcHZP45.

Funder

National Natural Science Foundation of China

Zhejiang Provincial Natural Science Foundation of China

Sichuan Province Fruit Tree Breeding Research

Fundamental Research Funds for the Central Universities, China

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Physiology

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