ArticleGenome biology2025
Translational regulation plasticity shapes wheat grain adaptation to heat stress.
Article in Genome biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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
2 citing papers in PubMed.
- Multi-Tissue Omics Analysis Uncovers Translational Regulation Underlying Complex Traits in Pigs.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Article
- Translational regulation plasticity shapes wheat grain adaptation to heat stress.Genome biology · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
Abstract
backgroundExtremely high temperatures due to global warming are increasingly threatening crop production, and plants have evolved highly sophisticated mechanisms to respond to harsh environmental stresses and survive. At the translational level, how bread wheat responds to high temperatures remains largely unknown.
resultsWe use ribosome profiling and high-throughput sequencing to investigate the translatome of wheat grains in response to high temperatures. Our study reveals that heat stress profoundly reshapes the translatomic landscapes, significantly affecting the translation of the mRNAs involved in the translation process, grain development, and heat stress response. A subset of the upstream open reading frames (uORFs) and RNA-binding proteins specifically link to their potential target with associated translatomic changes under high temperature. Divergent translation of duplicated genes is affected by the imbalanced expression of uORFs. Interestingly, the high temperature stimulates expression of small ORFs in long non-coding RNAs (lORFs). Microproteins encoded by key heat-responsive lORFs localize to cellular regions including the nucleus, endoplasmic reticulum, and P-body, and interact with heat shock proteins. Furthermore, the microprotein and RNA-binding protein contribute to the heat tolerance variation among wheat accessions.
conclusionsThis study provides new insights into the translational regulatory mechanism in wheat heat tolerance, accelerating genetic improvements in crops for optimal climate resilience.
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.