Evidence map›Paper›PMID 42078143›Full record

ArticleFrontiers in plant science2026

Autopolyploidization reshapes transcription factor regulatory networks and enhances MAPK-associated thermotolerance in rice.

Changjiang Zhang, Yu Wang, Xiaoyu Wang, Honglin Yuan, Yingkai Wang, Weilong Meng, Minghong Xu, Jian Ma, Ningning Wang

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Article in Frontiers in plant science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Changjiang Zhang *Faculty of Agronomy, Jilin Agricultural University, Changchun, China.
Yu Wang *Faculty of Agronomy, Jilin Agricultural University, Changchun, China.
Xiaoyu Wang *Faculty of Agronomy, Jilin Agricultural University, Changchun, China.
Honglin YuanFaculty of Agronomy, Jilin Agricultural University, Changchun, China.
Yingkai WangFaculty of Agronomy, Jilin Agricultural University, Changchun, China.
Weilong MengFaculty of Agronomy, Jilin Agricultural University, Changchun, China.
Minghong XuFaculty of Agronomy, Jilin Agricultural University, Changchun, China.
Jian MaFaculty of Agronomy, Jilin Agricultural University, Changchun, China.
Ningning WangFaculty of Agronomy, Jilin Agricultural University, Changchun, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polyploidization is an important evolutionary mechanism that contributes to plant adaptation to environmental stresses; however, the transcriptional regulatory mechanisms underlying enhanced thermotolerance in autopolyploid crops remain poorly understood. In our previous work, we demonstrated that the superior thermotolerance of tetraploid rice compared with diploid rice under heat stress was associated with DNA methylation and accompanied by differential expression of related genes. Nevertheless, the underlying molecular mechanisms remain to be further elucidated. In this study, we compared diploid japonica rice (GFD-2X) and its naturally derived autotetraploid counterpart (GFD-4X) under control, heat stress, and recovery conditions to investigate transcription factor (TF)-centered regulatory networks. Transcriptomic analysis identified 1,141 expressed TF genes across 56 families. Heat stress induced widespread transcriptional repression in both genotypes, with approximately 70% of differentially expressed TF genes (DETFs) downregulated. However, the autotetraploid genotype exhibited nearly threefold more genotype-specific DETFs under stress and demonstrated pronounced transcriptional reactivation during recovery, with upregulated DETFs exceeding downregulated genes by more than twofold. Family-level analysis revealed a regulatory shift from bHLH-dominated regulation during acute heat stress to WRKY- and MYB-associated modulation during recovery. Functional enrichment analysis highlighted hormone-mediated signaling and the mitogen-activated protein kinase (MAPK) signaling pathway as central regulatory components. Weighted gene co-expression network analysis (WGCNA) identified four modules positively associated with the autotetraploid genotype and 67 hub genes, including five MAPK-associated TFs (

Indexed as

autopolyploidizationgene co-expression networkheat stressMAPK signalingrice (Oryza sativa L.)transcription factors

Identifiers

PMID42078143
PMCPMC13128375

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.