Spatial distribution of proteins and metabolites in developing wheat grain and their differential regulatory response during the grain filling process

SUMMARY Grain filling and grain development are essential biological processes in the plant’s life cycle, eventually contributing to the final seed yield and quality in all cereal crops. Studies of how the different wheat (Triticum aestivum L.) grain components contribute to the overall development...

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Veröffentlicht in:The Plant journal : for cell and molecular biology 2021-08, Vol.107 (3), p.669-687
Hauptverfasser: Zhang, Shuang, Ghatak, Arindam, Bazargani, Mitra Mohammadi, Bajaj, Prasad, Varshney, Rajeev K., Chaturvedi, Palak, Jiang, Dong, Weckwerth, Wolfram
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container_issue 3
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container_title The Plant journal : for cell and molecular biology
container_volume 107
creator Zhang, Shuang
Ghatak, Arindam
Bazargani, Mitra Mohammadi
Bajaj, Prasad
Varshney, Rajeev K.
Chaturvedi, Palak
Jiang, Dong
Weckwerth, Wolfram
description SUMMARY Grain filling and grain development are essential biological processes in the plant’s life cycle, eventually contributing to the final seed yield and quality in all cereal crops. Studies of how the different wheat (Triticum aestivum L.) grain components contribute to the overall development of the seed are very scarce. We performed a proteomics and metabolomics analysis in four different developing components of the wheat grain (seed coat, embryo, endosperm, and cavity fluid) to characterize molecular processes during early and late grain development. In‐gel shotgun proteomics analysis at 12, 15, 20, and 26 days after anthesis (DAA) revealed 15 484 identified and quantified proteins, out of which 410 differentially expressed proteins were identified in the seed coat, 815 in the embryo, 372 in the endosperm, and 492 in the cavity fluid. The abundance of selected protein candidates revealed spatially and temporally resolved protein functions associated with development and grain filling. Multiple wheat protein isoforms involved in starch synthesis such as sucrose synthases, starch phosphorylase, granule‐bound and soluble starch synthase, pyruvate phosphate dikinase, 14‐3‐3 proteins as well as sugar precursors undergo a major tissue‐dependent change in abundance during wheat grain development suggesting an intimate interplay of starch biosynthesis control. Different isoforms of the protein disulfide isomerase family as well as glutamine levels, both involved in the glutenin macropolymer pattern, showed distinct spatial and temporal abundance, revealing their specific role as indicators of wheat gluten quality. Proteins binned into the functional category of cell growth/division and protein synthesis/degradation were more abundant in the early stages (12 and 15 DAA). At the metabolome level all tissues and especially the cavity fluid showed highly distinct metabolite profiles. The tissue‐specific data are integrated with biochemical networks to generate a comprehensive map of molecular processes during grain filling and developmental processes. Significance Statement We have applied a multiomics approach to analyze the grain filling process in wheat (Triticum aestivum L.). The spatial distribution of proteins and metabolites provides an integrated view of the biochemical networks during the developmental processes of the seed. This will provide the seed biologist with a comprehensive molecular map to improve the breeding process.
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Studies of how the different wheat (Triticum aestivum L.) grain components contribute to the overall development of the seed are very scarce. We performed a proteomics and metabolomics analysis in four different developing components of the wheat grain (seed coat, embryo, endosperm, and cavity fluid) to characterize molecular processes during early and late grain development. In‐gel shotgun proteomics analysis at 12, 15, 20, and 26 days after anthesis (DAA) revealed 15 484 identified and quantified proteins, out of which 410 differentially expressed proteins were identified in the seed coat, 815 in the embryo, 372 in the endosperm, and 492 in the cavity fluid. The abundance of selected protein candidates revealed spatially and temporally resolved protein functions associated with development and grain filling. Multiple wheat protein isoforms involved in starch synthesis such as sucrose synthases, starch phosphorylase, granule‐bound and soluble starch synthase, pyruvate phosphate dikinase, 14‐3‐3 proteins as well as sugar precursors undergo a major tissue‐dependent change in abundance during wheat grain development suggesting an intimate interplay of starch biosynthesis control. Different isoforms of the protein disulfide isomerase family as well as glutamine levels, both involved in the glutenin macropolymer pattern, showed distinct spatial and temporal abundance, revealing their specific role as indicators of wheat gluten quality. Proteins binned into the functional category of cell growth/division and protein synthesis/degradation were more abundant in the early stages (12 and 15 DAA). At the metabolome level all tissues and especially the cavity fluid showed highly distinct metabolite profiles. The tissue‐specific data are integrated with biochemical networks to generate a comprehensive map of molecular processes during grain filling and developmental processes. Significance Statement We have applied a multiomics approach to analyze the grain filling process in wheat (Triticum aestivum L.). The spatial distribution of proteins and metabolites provides an integrated view of the biochemical networks during the developmental processes of the seed. This will provide the seed biologist with a comprehensive molecular map to improve the breeding process.</description><identifier>ISSN: 0960-7412</identifier><identifier>EISSN: 1365-313X</identifier><identifier>DOI: 10.1111/tpj.15410</identifier><identifier>PMID: 34227164</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Biological activity ; Biosynthesis ; cavity fluid ; Cell growth ; Cereal crops ; Crop yield ; embryo ; Embryos ; Endosperm ; Gene Expression Regulation, Developmental ; Gene Expression Regulation, Plant ; Glutamine ; Gluten ; Glutenin ; Grain ; grain filling ; Isoforms ; Life cycles ; Metabolites ; Metabolomics ; Phosphorylase ; Plant Proteins - genetics ; Plant Proteins - metabolism ; Protein biosynthesis ; Protein disulfide-isomerase ; Protein synthesis ; Proteins ; Proteomics ; Pyruvate phosphate dikinase ; Pyruvic acid ; Resource ; seed coat ; Seed coats ; seed development ; Seeds - growth &amp; development ; Seeds - metabolism ; Shotguns ; Spatial distribution ; Starch ; Starch phosphorylase ; Starch synthase ; Sucrose ; Triticum - physiology ; Triticum aestivum ; Wheat</subject><ispartof>The Plant journal : for cell and molecular biology, 2021-08, Vol.107 (3), p.669-687</ispartof><rights>2021 The Authors. published by Society for Experimental Biology and John Wiley &amp; Sons Ltd.</rights><rights>2021 The Authors. 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Studies of how the different wheat (Triticum aestivum L.) grain components contribute to the overall development of the seed are very scarce. We performed a proteomics and metabolomics analysis in four different developing components of the wheat grain (seed coat, embryo, endosperm, and cavity fluid) to characterize molecular processes during early and late grain development. In‐gel shotgun proteomics analysis at 12, 15, 20, and 26 days after anthesis (DAA) revealed 15 484 identified and quantified proteins, out of which 410 differentially expressed proteins were identified in the seed coat, 815 in the embryo, 372 in the endosperm, and 492 in the cavity fluid. The abundance of selected protein candidates revealed spatially and temporally resolved protein functions associated with development and grain filling. Multiple wheat protein isoforms involved in starch synthesis such as sucrose synthases, starch phosphorylase, granule‐bound and soluble starch synthase, pyruvate phosphate dikinase, 14‐3‐3 proteins as well as sugar precursors undergo a major tissue‐dependent change in abundance during wheat grain development suggesting an intimate interplay of starch biosynthesis control. Different isoforms of the protein disulfide isomerase family as well as glutamine levels, both involved in the glutenin macropolymer pattern, showed distinct spatial and temporal abundance, revealing their specific role as indicators of wheat gluten quality. Proteins binned into the functional category of cell growth/division and protein synthesis/degradation were more abundant in the early stages (12 and 15 DAA). At the metabolome level all tissues and especially the cavity fluid showed highly distinct metabolite profiles. The tissue‐specific data are integrated with biochemical networks to generate a comprehensive map of molecular processes during grain filling and developmental processes. Significance Statement We have applied a multiomics approach to analyze the grain filling process in wheat (Triticum aestivum L.). The spatial distribution of proteins and metabolites provides an integrated view of the biochemical networks during the developmental processes of the seed. 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development</subject><subject>Seeds - metabolism</subject><subject>Shotguns</subject><subject>Spatial distribution</subject><subject>Starch</subject><subject>Starch phosphorylase</subject><subject>Starch synthase</subject><subject>Sucrose</subject><subject>Triticum - physiology</subject><subject>Triticum aestivum</subject><subject>Wheat</subject><issn>0960-7412</issn><issn>1365-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNp1kd9qFDEUxoModq1e-AIS8EYvpk0mmWRyI5TiXwoKVvAuZGbO7GbJJmOSadkX8XnNdNeigrlJOPmd73yHD6HnlJzRcs7ztD2jDafkAVpRJpqKUfb9IVoRJUglOa1P0JOUtoRQyQR_jE4Yr2tJBV-hn18nk61xeLApR9vN2QaPw4inGDJYn7DxA95BNl1wNkPC1uMBbsCFyfo1vt2AyXgdTSkvZN6AjUVsHCGCv1OOsJ6dySHuyzNNwSfAwxyX7kIfe0fr3FIpY3tI6Sl6NBqX4NnxPkXf3r29vvxQXX1-__Hy4qrqOWekGihI6IVRzDAQjFPJa9k1XMl24ECgbZjsuOpE3wpoetEDb8hIWuBcCcklO0VvDrrT3O1g6IvlaJyeot2ZuNfBWP33j7cbvQ43WtWKKqWKwKujQAw_ZkhZ72zqwTnjIcxJ1w1vFZGMLbNe_oNuwxx9Wa9QQpC6bMQL9fpA9TGkFGG8N0OJXtLWJW19l3ZhX_zp_p78HW8Bzg_ArXWw_7-Svv7y6SD5Cy8VuBI</recordid><startdate>202108</startdate><enddate>202108</enddate><creator>Zhang, Shuang</creator><creator>Ghatak, Arindam</creator><creator>Bazargani, Mitra Mohammadi</creator><creator>Bajaj, Prasad</creator><creator>Varshney, Rajeev K.</creator><creator>Chaturvedi, Palak</creator><creator>Jiang, Dong</creator><creator>Weckwerth, Wolfram</creator><general>Blackwell Publishing Ltd</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4562-9131</orcidid><orcidid>https://orcid.org/0000-0002-5856-0348</orcidid><orcidid>https://orcid.org/0000-0003-4706-9841</orcidid><orcidid>https://orcid.org/0000-0002-9719-6358</orcidid></search><sort><creationdate>202108</creationdate><title>Spatial distribution of proteins and metabolites in developing wheat grain and their differential regulatory response during the grain filling process</title><author>Zhang, Shuang ; 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Multiple wheat protein isoforms involved in starch synthesis such as sucrose synthases, starch phosphorylase, granule‐bound and soluble starch synthase, pyruvate phosphate dikinase, 14‐3‐3 proteins as well as sugar precursors undergo a major tissue‐dependent change in abundance during wheat grain development suggesting an intimate interplay of starch biosynthesis control. Different isoforms of the protein disulfide isomerase family as well as glutamine levels, both involved in the glutenin macropolymer pattern, showed distinct spatial and temporal abundance, revealing their specific role as indicators of wheat gluten quality. Proteins binned into the functional category of cell growth/division and protein synthesis/degradation were more abundant in the early stages (12 and 15 DAA). At the metabolome level all tissues and especially the cavity fluid showed highly distinct metabolite profiles. The tissue‐specific data are integrated with biochemical networks to generate a comprehensive map of molecular processes during grain filling and developmental processes. Significance Statement We have applied a multiomics approach to analyze the grain filling process in wheat (Triticum aestivum L.). The spatial distribution of proteins and metabolites provides an integrated view of the biochemical networks during the developmental processes of the seed. This will provide the seed biologist with a comprehensive molecular map to improve the breeding process.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>34227164</pmid><doi>10.1111/tpj.15410</doi><tpages>19</tpages><orcidid>https://orcid.org/0000-0002-4562-9131</orcidid><orcidid>https://orcid.org/0000-0002-5856-0348</orcidid><orcidid>https://orcid.org/0000-0003-4706-9841</orcidid><orcidid>https://orcid.org/0000-0002-9719-6358</orcidid><oa>free_for_read</oa></addata></record>
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subjects Biological activity
Biosynthesis
cavity fluid
Cell growth
Cereal crops
Crop yield
embryo
Embryos
Endosperm
Gene Expression Regulation, Developmental
Gene Expression Regulation, Plant
Glutamine
Gluten
Glutenin
Grain
grain filling
Isoforms
Life cycles
Metabolites
Metabolomics
Phosphorylase
Plant Proteins - genetics
Plant Proteins - metabolism
Protein biosynthesis
Protein disulfide-isomerase
Protein synthesis
Proteins
Proteomics
Pyruvate phosphate dikinase
Pyruvic acid
Resource
seed coat
Seed coats
seed development
Seeds - growth & development
Seeds - metabolism
Shotguns
Spatial distribution
Starch
Starch phosphorylase
Starch synthase
Sucrose
Triticum - physiology
Triticum aestivum
Wheat
title Spatial distribution of proteins and metabolites in developing wheat grain and their differential regulatory response during the grain filling process
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