MtGSTF7, a TT19-like GST gene, is essential for accumulation of anthocyanins, but not proanthocyanins in Medicago truncatula

Author:

Wang Ruoruo123ORCID,Lu Nan4,Liu Chenggang4,Dixon Richard A4ORCID,Wu Qing12,Mao Yawen12,Yang Yating15,Zheng Xiaoling12,He Liangliang1ORCID,Zhao Baolin1ORCID,Zhang Fan1,Yang Shengchao6,Chen Haitao7,Jun Ji Hyung4,Li Ying4,Liu Changning1,Liu Yu1,Chen Jianghua135ORCID

Affiliation:

1. CAS Key Laboratory of Tropical Plant Resources and Sustainable Use, CAS Center for Excellence for Molecular Plant Science, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Kunming , Yunnan 650223 , China

2. University of Chinese Academy of Sciences , Beijing 100049 , China

3. Yunnan Key Laboratory of Plant Reproductive Adaptation and Evolutionary Ecology and Institute of Biodiversity, School of Ecology and Environmental Science, Yunnan University , Kunming, Yunnan 650500 , China

4. BioDiscovery Institute and Department of Biological Sciences, University of North Texas , Denton, TX 76203 , USA

5. School of Life Science, University of Science and Technology of China , Hefei, Anhui 230026 , China

6. National and Local Joint Engineering Research Center on Germplasm Innovation and Utilization of Chinese Medicinal Materials in Southwest China, Yunnan Agricultural University , Kunming, Yunnan 650201 , China

7. Sanjie Institute of Forage , Yangling, Shaanxi 712100 , China

Abstract

Abstract Anthocyanins and proanthocyanins (PAs) are two end products of the flavonoid biosynthesis pathway. They are believed to be synthesized in the endoplasmic reticulum and then sequestered into the vacuole. In Arabidopsis thaliana, TRANSPARENT TESTA 19 (TT19) is necessary for both anthocyanin and PA accumulation. Here, we found that MtGSTF7, a homolog of AtTT19, is essential for anthocyanin accumulation but not required for PA accumulation in Medicago truncatula. MtGSTF7 was induced by the anthocyanin regulator LEGUME ANTHOCYANIN PRODUCTION 1 (LAP1), and its tissue expression pattern correlated with anthocyanin deposition in M. truncatula. Tnt1-insertional mutants of MtGSTF7 lost anthocyanin accumulation in vegetative organs, and introducing a genomic fragment of MtGSTF7 could complement the mutant phenotypes. Additionally, the accumulation of anthocyanins induced by LAP1 was significantly reduced in mtgstf7 mutants. Yeast-one-hybridization and dual-luciferase reporter assays revealed that LAP1 could bind to the MtGSTF7 promoter to activate its expression. Ectopic expression of MtGSTF7 in tt19 mutants could rescue their anthocyanin deficiency, but not their PA defect. Furthermore, PA accumulation was not affected in the mtgstf7 mutants. Taken together, our results show that the mechanism of anthocyanin and PA accumulation in M. truncatula is different from that in A. thaliana, and provide a new target gene for engineering anthocyanins in plants.

Funder

Strategic Priority Research Program of the Chinese Academy of Sciences

National Natural Science Foundation of China

High-end Scientific and Technological Talents in Yunnan Province

Yunnan Fundamental Research Projects

Youth Innovation Promotion Association CAS

National Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Physiology

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