Integration of cell differentiation and initiation of monoterpenoid indole alkaloid metabolism in seed germination of Catharanthus roseus

Author:

Uzaki Mai12ORCID,Mori Tetsuya2ORCID,Sato Mayuko2,Wakazaki Mayumi2,Takeda‐Kamiya Noriko2,Yamamoto Kotaro3ORCID,Murakami Akio4ORCID,Guerrero Delia Ayled Serna5ORCID,Shichijo Chizuko4,Ohnishi Miwa46,Ishizaki Kimitsune4ORCID,Fukaki Hidehiro4ORCID,O'Connor Sarah E.5ORCID,Toyooka Kiminori2ORCID,Mimura Tetsuro4789ORCID,Hirai Masami Yokota12ORCID

Affiliation:

1. Graduate School of Bioagricultural Science Nagoya University Nagoya Aichi 464‐8601 Japan

2. RIKEN Center for Sustainable Resource Science Yokohama Kanagawa 230‐0045 Japan

3. School of Science Yokohama City University Yokohama Kanagawa 236‐0027 Japan

4. Graduate School of Science Kobe University Kobe Hyogo 657‐8501 Japan

5. Department of Natural Product Biosynthesis Max Planck Institute for Chemical Ecology Jena D‐07745 Germany

6. Graduate School of Science Kyoto University Kyoto 606‐8502 Japan

7. College of Bioscience and Biotechnology National Cheng Kung University Tainan 70101 Taiwan

8. The Institute for Sustainable Agro‐ecosystem Services, Graduate School of Agricultural and Life Sciences The University of Tokyo Tokyo 188‐0002 Japan

9. Faculty of Bioenvironmental Sciences Kyoto University of Advanced Science Kyoto 621‐8555 Japan

Abstract

Summary In Catharanthus roseus, monoterpenoid indole alkaloids (MIAs) are produced through the cooperation of four cell types, with final products accumulating in specialized cells known as idioblasts and laticifers. To explore the relationship between cellular differentiation and cell type‐specific MIA metabolism, we analyzed the expression of MIA biosynthesis in germinating seeds. Embryos from immature and mature seeds were observed via stereomicroscopy, fluorescence microscopy, and electron microscopy. Time‐series MIA and iridoid quantification, along with transcriptome analysis, were conducted to determine the initiation of MIA biosynthesis. In addition, the localization of MIAs was examined using alkaloid staining and imaging mass spectrometry (IMS). Laticifers were present in embryos before seed maturation. MIA biosynthesis commenced 12 h after germination. MIAs accumulated in laticifers of embryos following seed germination, and MIA metabolism is induced after germination in a tissue‐specific manner. These findings suggest that cellular morphological differentiation precedes metabolic differentiation. Considering the well‐known toxicity and defense role of MIAs in matured plants, MIAs may be an important defense strategy already in the delicate developmental phase of seed germination, and biosynthesis and accumulation of MIAs may require the tissue and cellular differentiation.

Funder

Japan Society for the Promotion of Science

Japan Science and Technology Agency

Publisher

Wiley

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