Evidence map›Paper›PMID 41184875›Full record

ArticleBMC biology2025

Genomic and translational insights into eIF2B-mediated salt tolerance in sea rice HD961.

Haomin Chen, Mingming Chen, Shan Yang, Hongkai Zhou, Zhihao Xie, Yongxiang Huang, Daming Chen

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In one paragraph

Article in BMC 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
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Haomin Chen *College of Coastal Agricultural Sciences, Guangdong Ocean University, Zhanjiang, 524008, China.
Mingming Chen *College of Coastal Agricultural Sciences, Guangdong Ocean University, Zhanjiang, 524008, China. mingming.chen@gdou.edu.cn.
Shan Yang *College of Coastal Agricultural Sciences, Guangdong Ocean University, Zhanjiang, 524008, China.
Hongkai ZhouCollege of Coastal Agricultural Sciences, Guangdong Ocean University, Zhanjiang, 524008, China.
Zhihao XieCollege of Coastal Agricultural Sciences, Guangdong Ocean University, Zhanjiang, 524008, China.
Yongxiang HuangCollege of Coastal Agricultural Sciences, Guangdong Ocean University, Zhanjiang, 524008, China.
Daming ChenCollege of Coastal Agricultural Sciences, Guangdong Ocean University, Zhanjiang, 524008, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSoil salinization threatens global rice production, driving the urgent need for salt-tolerant rice cultivars. Sea rice HD961, renowned for its exceptional salt tolerance, serves as an ideal model for elucidating molecular adaptations to salinity.

resultsIn this study, we generated a high-quality, chromosome-level genome assembly of HD961 using Nanopore long-read sequencing, Illumina short-read polishing, and Hi-C-based scaffolding, providing a robust foundation for translatomic analysis. To explore translational responses to salt stress, we integrated ribosome profiling (Ribo-seq) with the QEZ-seq protocol and RNA sequencing (RNA-seq) under 150 mM NaCl conditions. Our results reveal that salt stress selectively enhances translational efficiency (TE) in genes critical for ion homeostasis, antioxidant defense, and cell wall remodeling, enabling HD961 to maintain cellular balance under stress. Especially, eukaryotic translation initiation factor 2B (eIF2B) emerged as a key regulator, with its upregulation and the formation of stress-induced eIF2B-containing bodies indicating a novel mechanism to optimize protein synthesis. Additionally, ribosome footprint profiling revealed codon-specific modulation of A-site dwell times, with the GCG codon showing a particularly pronounced shift under salt stress, suggesting fine-tuned translational control that prioritizes stress-responsive proteins.

conclusionTogether, these findings highlight eIF2B-mediated translational regulation as central to HD961's salt tolerance, offering valuable genomic and translatomic resources for breeding salt-tolerant rice and other crops.

Indexed as

Genome, PlantOryzaPlant ProteinsProtein BiosynthesisSalt ToleranceGene Expression Regulation, PlantPlant ProteinseIF2BHD961Ribosome profilingSalt stressTranslation regulation

Identifiers

PMID41184875
PMCPMC12581241

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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.