Molecular identification of phenylalanine ammonia lyase-encoding genes EfPALs and EfPAL2-interacting transcription factors in Euryale ferox

AiLian Liu; Yue Zhu; YuHao Wang; TianYu Wang; ShuPing Zhao; Kai Feng; LiangJun Li; Peng Wu

doi:10.3389/fpls.2023.1114345

Molecular identification of phenylalanine ammonia lyase-encoding genes EfPALs and EfPAL2-interacting transcription factors in Euryale ferox

Front Plant Sci. 2023 Mar 21:14:1114345. doi: 10.3389/fpls.2023.1114345. eCollection 2023.

Authors

AiLian Liu¹, Yue Zhu¹, YuHao Wang¹, TianYu Wang¹, ShuPing Zhao¹, Kai Feng¹, LiangJun Li^{1

2}, Peng Wu^{1

2}

Affiliations

¹ College of Horticulture and Landscape Architecture, Yangzhou, Jiangsu, China.
² Joint International Research Laboratory of Agriculture and Agri-Product Safety of Ministry of Education of China, Yangzhou University, Yangzhou, China.

Abstract

Flavonoids are one of the most important secondary metabolites in plants, and phenylalanine ammonia-lyase (PAL) is the first rate-limiting enzyme for their biosynthesis. However, detailed information on the regulation of PAL in plants is still little. In this study, PAL in E. ferox was identified and functionally analyzed, and its upstream regulatory network was investigated. Through genome-wide identification, we obtained 12 putative PAL genes from E. ferox. Phylogenetic tree and synteny analysis revealed that PAL in E. ferox was expanded and mostly preserved. Subsequently, enzyme activity assays demonstrated that EfPAL1 and EfPAL2 both catalyzed the production of cinnamic acid from phenylalanine only, with EfPAL2 exhibiting a superior enzyme activity. Overexpression of EfPAL1 and EfPAL2 in Arabidopsis thaliana, respectively, both enhanced the biosynthesis of flavonoids. Furthermore, two transcription factors, EfZAT11 and EfHY5, were identified by yeast one-hybrid library assays as binding to the promoter of EfPAL2, and further luciferase (LUC) activity analysis indicated that EfZAT11 promoted the expression of EfPAL2, while EfHY5 repressed the expression of EfPAL2. These results suggested that EfZAT11 and EfHY5 positively and negatively regulate flavonoid biosynthesis, respectively. Subcellular localization revealed that EfZAT11 and EfHY5 were localized in the nucleus. Our findings clarified the key EfPAL1 and EfPAL2 of flavonoid biosynthesis in E. ferox and established the upstream regulatory network of EfPAL2, which would provide novel information for the study of flavonoid biosynthesis mechanism.

Keywords: HY5; ZAT11; flavonoids; phenylalanine ammonia-lyase (PAL); transcriptional regulation.

Grants and funding

This work was supported by the National Natural Science Foundation of China (grant number: 31902002), China Postdoctoral Science Foundation (grant number: 2020T130706), China Agriculture Research System (grant number: CARS-24), Jiangsu seed industry revitalization’Jie Bang Gua Shuai’project (grant number: JBGS [2021]017), and Postgraduate Research and Practice Innovation Program in Jiangsu Province (grant number: KYCX22_3522).