Cell‐type proteomic and metabolomic resolution of early and late grain filling stages of wheat endosperm

Author:

Zhang Shuang12ORCID,Ghatak Arindam13ORCID,Mohammadi Bazargani Mitra4ORCID,Kramml Hannes1ORCID,Zang Fujuan2,Gao Shuang2,Ramšak Živa5ORCID,Gruden Kristina5ORCID,Varshney Rajeev K.6ORCID,Jiang Dong2ORCID,Chaturvedi Palak1ORCID,Weckwerth Wolfram13ORCID

Affiliation:

1. Molecular Systems Biology Lab (MOSYS), Department of Functional and Evolutionary Ecology University of Vienna Vienna Austria

2. National Technique Innovation Center for Regional Wheat Production/Key Laboratory of Crop Ecophysiology Ministry of Agriculture/Nanjing Agricultural University Nanjing China

3. Vienna Metabolomics Center (VIME) University of Vienna Vienna Austria

4. Agriculture Institute Iranian Research Organization for Science and Technology Tehran Iran

5. Department of Systems Biology and Biotechnology, National Institute of Biology Ljubljana Slovenia

6. State Agricultural Biotechnology Centre, Centre for Crop and Food Innovation, Food Futures Institute Murdoch University Murdoch WA Australia

Abstract

SummaryThe nutritional value of wheat grains, particularly their protein and metabolite composition, is a result of the grain‐filling process, especially in the endosperm. Here, we employ laser microdissection (LMD) combined with shotgun proteomics and metabolomics to generate a cell type‐specific proteome and metabolome inventory of developing wheat endosperm at the early (15 DAA) and late (26 DAA) grain‐filling stages. We identified 1803 proteins and 41 metabolites from four different cell types (aleurone (AL), sub‐aleurone (SA), starchy endosperm (SE) and endosperm transfer cells (ETCs). Differentially expressed proteins were detected, 67 in the AL, 31 in the SA, 27 in the SE and 50 in the ETCs between these two‐time points. Cell‐type accumulation of specific SUT and GLUT transporters, sucrose converting and starch biosynthesis enzymes correlate well with the respective sugar metabolites, suggesting sugar upload and starch accumulation via nucellar projection and ETC at 15 DAA in contrast to the later stage at 26 DAA. Changes in various protein levels between AL, SA and ETC support this metabolic switch from 15 to 26 DAA. The distinct spatial and temporal abundances of proteins and metabolites revealed a contrasting activity of nitrogen assimilation pathways, e.g. for GOGAT, GDH and glutamic acid, in the different cell types from 15 to 26 DAA, which can be correlated with specific protein accumulation in the endosperm. The integration of cell‐type specific proteome and metabolome data revealed a complex metabolic interplay of the different cell types and a functional switch during grain development and grain‐filling processes.

Funder

Austrian Science Fund

China Scholarship Council

Horizon 2020 Framework Programme

Publisher

Wiley

Subject

Plant Science,Agronomy and Crop Science,Biotechnology

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