Evidence map›Paper›PMID 41299134›Full record

ArticleStress biology2025

OsNTL2 confers rice osmotic stress resilience through coordinated transcriptional regulation of the ASC-GSH redox cycle and cell wall biosynthesis.

Heng Zhou, Xiaoyun Ma, Jianping Yang, Lingxi Geng, Taotao Qiu, Xinyue Fan, Kailu Zhang, Fuyuan Zhu, Yanjie Xie

Abstract read
In one paragraph

Article in Stress biology, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Heng Zhou *Laboratory Center of Life Sciences, College of Life Sciences, Nanjing Agricultural University, Nanjing, 210095, China.
Xiaoyun Ma *Laboratory Center of Life Sciences, College of Life Sciences, Nanjing Agricultural University, Nanjing, 210095, China.
Jianping Yang *Laboratory Center of Life Sciences, College of Life Sciences, Nanjing Agricultural University, Nanjing, 210095, China.
Lingxi GengLaboratory Center of Life Sciences, College of Life Sciences, Nanjing Agricultural University, Nanjing, 210095, China.
Taotao QiuLaboratory Center of Life Sciences, College of Life Sciences, Nanjing Agricultural University, Nanjing, 210095, China.
Xinyue FanLaboratory Center of Life Sciences, College of Life Sciences, Nanjing Agricultural University, Nanjing, 210095, China.
Kailu ZhangNational Key Laboratory for the Development and Utilization of Forest Food Resources, Co-Innovation Center for Sustainable Forestry in Southern China, State Key Laboratory of Tree Genetics and Breeding, Key Laboratory of State Forestry and Grassland Administration On Subtropical Forest Biodiversity Conservation, College of Life Sciences, Nanjing Forestry University, Nanjing, 210037, Jiangsu, China.
Fuyuan ZhuNational Key Laboratory for the Development and Utilization of Forest Food Resources, Co-Innovation Center for Sustainable Forestry in Southern China, State Key Laboratory of Tree Genetics and Breeding, Key Laboratory of State Forestry and Grassland Administration On Subtropical Forest Biodiversity Conservation, College of Life Sciences, Nanjing Forestry University, Nanjing, 210037, Jiangsu, China.
Yanjie XieLaboratory Center of Life Sciences, College of Life Sciences, Nanjing Agricultural University, Nanjing, 210095, China. yjxie@njau.edu.cn.ORCID http://orcid.org/0000-0002-3503-1267

Funding

Natural Science Foundation of China 32470299Science Fund for Distinguished Young Scholars of Jiangsu Province BK20220084the STI 2030-Major Projects 2023ZD040562
6 · The paper itself

Abstract

Drought, high salinity, and low temperatures impose osmotic stress, hindering water uptake and severely limiting plant growth and crop productivity. Osmotic stress not only perturbs cellular osmotic homeostasis but also disrupts multiple metabolic processes, including reactive oxygen species (ROS) metabolism. However, the transcriptional regulation underlying these redox processes in plants remains poorly understood. Here, we report that rice NAC WITH TRANS-MEMBRANE MOTIF1- LIKE 2 (OsNTL2) is required for tolerance to salt and osmotic stresses. DNA affinity purification-sequencing (DAP-seq) revealed that OsNTL2 directly targets key genes in the ascorbate-glutathione (ASC-GSH) redox cycle, including ascorbate peroxidase 2 (APX2), monodehydroascorbate reductase 1 (MDHAR1), glutathione reductase 2 (GR2), and glutathione peroxidase 5 (GPX5), as well as peroxidase 3/70 (PRX3/70), which function in the hydrogen peroxide catabolic process. Consistently, OsNTL2 activity was associated with enhanced ASC-GSH cycle enzyme activities, elevated ASC and GSH contents, and reduced ROS accumulation, as confirmed by histochemical staining. Furthermore, integrating DAP-seq with transcriptome analysis, we identified 325 direct transcriptional targets of OsNTL2, with a significant enrichment of genes involved in lignin and xylan biosynthesis. Notably, OsNTL2 bound directly to the promoters of, 4-coumarate-CoA ligase 5 (Os4CL5), and cinnamoyl-CoA reductase (OsCCR), activating their transcription. Correspondingly, stress-induced lignin, xylan, and cellulose accumulation was markedly reduced in ntl2 mutants but enhanced in OsNTL2-overexpressing lines. Together, these findings identify OsNTL2 as a key transcriptional regulator that coordinates the ASC-GSH redox cycle and cell wall biosynthesis to confer osmotic stress tolerance in rice.

Indexed as

ASC-GSH cycleCell wallNAC TFOsmotic stressTranscriptional regulation

Identifiers

PMID41299134
PMCPMC12657681

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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.