Evidence map›Paper›PMID 40604394›Full record

ArticleBMC plant biology2025

Proteomic profiling reveals important regulators of photosynthate accumulation in wheat leaves during grain development.

Wanting Li, Xiangrui Liu, Zeyu Shi, Yifei Wang, Wenqiang Tang, Huimin Ren, Baowen Zhang

Abstract read
In one paragraph

Article in BMC plant biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Wanting Li *Ministry of Education Key Laboratory of Molecular and Cellular Biology, Shijiazhuang, China.
Xiangrui Liu *Ministry of Education Key Laboratory of Molecular and Cellular Biology, Shijiazhuang, China.
Zeyu ShiMinistry of Education Key Laboratory of Molecular and Cellular Biology, Shijiazhuang, China.
Yifei WangMinistry of Education Key Laboratory of Molecular and Cellular Biology, Shijiazhuang, China.
Wenqiang TangMinistry of Education Key Laboratory of Molecular and Cellular Biology, Shijiazhuang, China.
Huimin RenMinistry of Education Key Laboratory of Molecular and Cellular Biology, Shijiazhuang, China. renhuimin858@163.com.
Baowen ZhangMinistry of Education Key Laboratory of Molecular and Cellular Biology, Shijiazhuang, China. zhangbw@hebtu.edu.cn.

Funding

Science Research Project of Hebei Education Department BJ2021029the Doctoral Initial Funding Project of Hebei Normal University L2024B58the Graduate innovation Funding Project of Hebei Normal University XCXZZSS202337the High-Level Talent Team Construction Project of Hebei Province 225A2902D
6 · The paper itself

Abstract

backgroundWheat yield potential is intrinsically linked to the efficiency of photosynthetic carbon fixation and subsequent allocation to developing grains. While leaves are recognized as the dominant source of photosynthate, the molecular drivers governing temporal shifts in source tissue function during grain filling remain unresolved, leaving a critical gap in knowledge about the proteomic reprogramming underlying natural developmental transitions. Addressing this gap could reveal novel targets for enhancing carbohydrate partitioning efficiency and improving agronomic yield in wheat.

resultsThis study presents a comprehensive temporal proteomic analysis of wheat source tissues (the flag leaf and -2nd leaf), from the initiation of the grain filling stage to the termination of source-to-sink transport (10-40 days after anthesis, DAA), using a data-independent acquisition (DIA)-based proteomics approach. Weighted gene co-expression network analysis (WGCNA) identified significant enrichment of photosynthesis-related proteins, carbohydrate metabolic enzymes, and cytokinin metabolic enzymes during the early grain filling stage (10-15 DAA). Integrated co-expression clustering and multiple expectation maximizations for motif elicitation (MEME) analysis revealed strong enrichment of Dof (DNA binding with one finger) transcription factor binding cis-elements in the promoters of carbohydrate synthesis-related genes. Additionally, through haplotype-phenotype association studies, we identified favorable Dof family haplotypes that were significantly associated with increased thousand-grain weight (TGW) and enhanced leaf chlorophyll content.

conclusionsOur findings not only provided a systematic characterization of proteome dynamics in wheat source tissues during the grain filling stage, but also revealed several key regulatory proteins that may control carbohydrate accumulation in source tissues, offering potential new targets for breeding strategies aimed at improving wheat yield.

Indexed as

Edible GrainPhotosynthesisPlant LeavesPlant ProteinsProteomeTriticumGene Expression Regulation, PlantProteomicsSeedsPlant ProteinsProteomeCKXsDIA-based proteomicsDofSource-to-sink transportWheat

Identifiers

PMID40604394
PMCPMC12220436

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