Comparative metabolomics and transcriptomics of pistils, stamens and pistilloid stamens widen key knowledge of pistil and stamen development in wheat
Yan Yu,
Zheng Song Peng,
Ji Peng Qu,
Zhen Yong Chen,
Shu Hong Wei,
Ming Li Liao,
Li Zhang and
Zai Jun Yang
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Yan Yu: Key Laboratory of Southwest China Wildlife Resources Conservation (Ministry of Education), College of Life Science, China West Normal University, Nanchong, Sichuan, P.R. China
Zheng Song Peng: School of Agricultural Science, Xichang University, Xichang, Sichuan, P.R. China
Ji Peng Qu: School of Agricultural Science, Xichang University, Xichang, Sichuan, P.R. China
Zhen Yong Chen: Key Laboratory of Southwest China Wildlife Resources Conservation (Ministry of Education), College of Life Science, China West Normal University, Nanchong, Sichuan, P.R. China
Shu Hong Wei: Key Laboratory of Southwest China Wildlife Resources Conservation (Ministry of Education), College of Life Science, China West Normal University, Nanchong, Sichuan, P.R. China
Ming Li Liao: Key Laboratory of Southwest China Wildlife Resources Conservation (Ministry of Education), College of Life Science, China West Normal University, Nanchong, Sichuan, P.R. China
Li Zhang: College of Sciences, Sichuan Agricultural University, Ya'an, Sichuan, P.R. China
Zai Jun Yang: Key Laboratory of Southwest China Wildlife Resources Conservation (Ministry of Education), College of Life Science, China West Normal University, Nanchong, Sichuan, P.R. China
Czech Journal of Genetics and Plant Breeding, 2020, vol. 56, issue 1, 24-33
Abstract:
To examine the role of metabolites in wheat stamen and pistil development, metabolomic analyses of pistilloid stamens (PS), pistils (P), and stamens (S) from a novel wheat mutant homologous transformation sterility-1 (HTS-1) and controls from their sib-line CSTP were conducted using base gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS). Then, the metabolomic data were integrated with previously published transcriptomic data and analysed. In total, 141 annotated metabolites were determined from P, PS and S tissues by comparison with reference standards. A total of 90, 93 and 18 different metabolites were identified in S vs. PS, S vs. P and P vs. PS, respectively. Among the different metabolites, 80 may be associated with stamen and pistil growth. Using integration evaluations of both the previous transcriptome data and the 80 various metabolites, we found two perturbed pathways that significantly affect flower development in plants, namely, the phenylpropanoid biosynthesis and cysteine and methionine metabolism. The ethylene synthesis pathway, one key branch of the cysteine and methionine metabolic pathways, could have a pivotal role in pistillody growth involving HTS-1. We found two key enzyme genes in the ethylene synthesis pathway (the SAM synthase gene and the ACC synthase gene) that have higher expression levels in stamens than in pistilloid stamens or pistils. We speculate, that the decrease in ethylene content during stamen development leads to pistillody traits in HTS-1. This study helps elucidate the molecular mechanisms underlying stamen and pistil growth in wheat.
Keywords: metabolome; pistillody; transcriptome; Triticum aestivum L.; wheat (search for similar items in EconPapers)
Date: 2020
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Persistent link: https://EconPapers.repec.org/RePEc:caa:jnlcjg:v:56:y:2020:i:1:id:70-2019-cjgpb
DOI: 10.17221/70/2019-CJGPB
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