ArticleStress biology2025
OsNTL2 confers rice osmotic stress resilience through coordinated transcriptional regulation of the ASC-GSH redox cycle and cell wall biosynthesis.
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.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
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
Identifiers
What OpenQuestion holds
Registered trials
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.