High-resolution genome mapping and functional dissection of chlorogenic acid production in Lonicera maackii

Author:

Li Ruili123ORCID,Xu Jing123ORCID,Qi Zengxing123ORCID,Zhao Shiwei123ORCID,Zhao Ran123,Ge Yanrui123,Li Ruofan123ORCID,Kong Xiuya4ORCID,Wu Zhenying4ORCID,Zhang Xi123ORCID,He Qizouhong123,Zhang Yan123ORCID,Liu Ping-Li123ORCID,Zhu Lei123,Mao Jian-Feng123ORCID,Fu Chunxiang4ORCID,Komis George5,Grünhofer Paul6ORCID,Schreiber Lukas6ORCID,Lin Jinxing123ORCID

Affiliation:

1. State Key Laboratory of Tree Genetics and Breeding, College of Biological Sciences and Technology, Beijing Forestry University , Beijing 100083 , China

2. National Engineering Research Center of Tree Breeding and Ecological Restoration, College of Biological Sciences and Technology, Beijing Forestry University , Beijing 100083 , China

3. Institute of Tree Development and Genome Editing, Beijing Forestry University , Beijing 100083 , China

4. Shandong Provincial Key Laboratory of Energy Genetics and CAS Key Laboratory of Biofuels, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences , Qingdao, Shandong 266101 , China

5. Department of Botany, School of Biology, Aristotle University of Thessaloniki , 54124 Thessaloniki , Greece

6. Department of Ecophysiology, Institute of Cellular and Molecular Botany, University of Bonn , Kirschallee 1, 53115 Bonn , Germany

Abstract

Abstract Amur honeysuckle (Lonicera maackii) is a widely used medicinal plant of the Caprifoliaceae family that produces chlorogenic acid. Research on this plant mainly focuses on its ornamental value and medicinal compounds, but a reference genome sequence and molecular resources for accelerated breeding are currently lacking. Herein, nanopore sequencing and high-throughput chromosome conformation capture (Hi-C) allowed a chromosome-level genome assembly of L. maackii (2n = 18). A global view of the gene regulatory network involved in the biosynthesis of chlorogenic acid and the dynamics of fruit coloration in L. maackii was established through metabolite profiling and transcriptome analyses. Moreover, we identified the genes encoding hydroxycinnamoyl-CoA quinate transferase (LmHQT) and hydroxycinnamoyl-CoA shikimic/quinate transferase (LmHCT), which localized to the cytosol and nucleus. Heterologous overexpression of these genes in Nicotiana benthamiana leaves resulted in elevated chlorogenic acid contents. Importantly, HPLC analyses revealed that LmHCT and LmHQTs recombinant proteins modulate the accumulation of chlorogenic acid (CGA) using quinic acid and caffeoyl CoA as substrates, highlighting the importance of LmHQT and LmHCT in CGA biosynthesis. These results confirmed that LmHQTs and LmHCT catalyze the biosynthesis of CGA in vitro. The genomic data presented in this study will offer a valuable resource for the elucidation of CGA biosynthesis and facilitating selective molecular breeding.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Program of Introducing Talents of Discipline to Universities

Fundamental Research Funds for the Central Universities

National Training Program of Innovation and Entrepreneurship for Undergraduates

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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