Spatiotemporal transcriptomics and metabolic profiling provide insights into gene regulatory networks during lentil seed development

Author:

Yu Bianyun1,Gao Peng2,Song Jingpu1,Yang Hui1,Qin Li3,Yu Xiaoyu3,Song Halim1,Coulson Justin1,Bekkaoui Yasmina1,Akhov Leonid1,Han Xiumei1,Cram Dustin1,Wei Yangdou4,Zaharia L. Irina1,Zou Jitao1,Konkin David1,Quilichini Teagen D.1,Fobert Pierre5,Patterson Nii1,Datla Raju3,Xiang Daoquan1ORCID

Affiliation:

1. Aquatic and Crop Resource Development National Research Council Canada Saskatoon Saskatchewan S7N 0W9 Canada

2. Agriculture and Agri‐Food Canada Saskatoon Research and Development Centre 107 Science Place Saskatoon SK S7N 0X2 Canada

3. Global Institute for Food Security University of Saskatchewan Saskatoon SK S7N 4L8 Canada

4. College of Art & Science University of Saskatchewan 9 Campus Drive Saskatoon SK S7N 5A5 Canada

5. Aquatic and Crop Resource Development National Research Council Canada Ottawa Ontario K1A 0R6 Canada

Abstract

SUMMARYLentil (Lens culinaris Medik.) is a nutritious legume with seeds rich in protein, minerals and an array of diverse specialized metabolites. The formation of a seed requires regulation and tight coordination of developmental programs to form the embryo, endosperm and seed coat compartments, which determines the structure and composition of mature seed and thus its end‐use quality. Understanding the molecular and cellular events and metabolic processes of seed development is essential for improving lentil yield and seed nutritional value. However, such information remains largely unknown, especially at the seed compartment level. In this study, we generated high‐resolution spatiotemporal gene expression profiles in lentil embryo, seed coat and whole seeds from fertilization through maturation. Apart from anatomic differences between the embryo and seed coat, comparative transcriptomics and weighted gene co‐expression network analysis revealed embryo‐ and seed coat‐specific genes and gene modules predominant in specific tissues and stages, which highlights distinct genetic programming. Furthermore, we investigated the dynamic profiles of flavonoid, isoflavone, phytic acid and saponin in seed compartments across seed development. Coupled with transcriptome data, we identified sets of candidate genes involved in the biosynthesis of these metabolites. The global view of the transcriptional and metabolic changes of lentil seed tissues throughout development provides a valuable resource for dissecting the genetic control of secondary metabolism and development of molecular tools for improving seed nutritional quality.

Publisher

Wiley

Subject

Cell Biology,Plant Science,Genetics

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