Abstract

BackgroundTo understand the mechanism of glucosinolates (GSs) accumulation in the specific organs, combined analysis of physiological change and transcriptome sequencing were applied in the current study. Taking Chinese kale as material, seeds and silique walls were divided into different stages based on the development of the embryo in seeds and then subjected to GS analysis and transcriptome sequencing.ResultsThe main GS in seeds of Chinese kale were glucoiberin and gluconapin and their content changed with the development of the seed. During the transition of the embryo from torpedo- to the early cotyledonary-embryo stage, the accumulation of GS in the seed was accompanied by the salient decline of GS in the corresponding silique wall. Thus, the seed and corresponding silique wall at these two stages were subjected to transcriptomic sequencing analysis. 135 genes related to GS metabolism were identified, of which 24 genes were transcription factors, 81 genes were related to biosynthetic pathway, 25 genes encoded catabolic enzymes, and 5 genes matched with transporters. The expression of GS biosynthetic genes was detected both in seeds and silique walls. The high expression of FMOGS-OX and AOP2, which is related to the production of gluconapin by side modification, was noted in seeds at both stages. Interestingly, the expression of GS biosynthetic genes was higher in the silique wall compared with that in the seed albeit lower content of GS existed in the silique wall than in the seed. Combined with the higher expression of transporter genes GTRs in silique walls than in seeds, it was proposed that the transportation of GS from the silique wall to the seed is an important source for seed GS accumulation. In addition, genes related to GS degradation expressed abundantly in the seed at the early cotyledonary-embryo stage indicating its potential role in balancing seed GS content.ConclusionsTwo stages including the torpedo-embryo and the early cotyledonary-embryo stage were identified as crucial in GS accumulation during seed development. Moreover, we confirmed the transportation of GS from the silique wall to the seed and proposed possible sidechain modification of GS biosynthesis may exist during seed formation.

Highlights

  • To understand the mechanism of glucosinolates (GSs) accumulation in the specific organs, combined analysis of physiological change and transcriptome sequencing were applied in the current study

  • We have identified genes related to GS metabolism in Chinese kale sprouts [3]

  • By physiological analysis of GS accumulation with development of the seed and corresponding silique wall, we have identified the crucial stages for GS transition, that was torpedo- and cotyledonary-embryo, and these two stages were subjected to the transcriptome analysis after RNA sequencing

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Summary

Introduction

To understand the mechanism of glucosinolates (GSs) accumulation in the specific organs, combined analysis of physiological change and transcriptome sequencing were applied in the current study. Taking Chinese kale as material, seeds and silique walls were divided into different stages based on the development of the embryo in seeds and subjected to GS analysis and transcriptome sequencing. Glucosinolates are a class of steroid glycosides synthesized from glucose and amino acids. These compounds widely occur as secondary metabolites in cruciferous species, especially Arabidopsis and a large number of economically valuable vegetables [5,6,7]. Based on the amino acids from which the compounds are derived, GS can be categorized into aliphatic GS, indolic GS, and aromatic GS [8, 9]. Indolic GSs act against phloem feeders and pathogens [13], whereas aliphatic, indolic, and benzyl GS may affect the performance of chewing insects [14]

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