ReviewPlant, cell & environment2026
Mitochondrial-Nuclear Interactions, Co-Transcription, and Adaptive Evolution in Cytoplasmic Male Sterility.
Review in Plant, cell & environment, 2026. 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.
- Revisiting the Molecular Roadmap for Sugar Crops: Genome Reading, Trait Writing and Variety Redesigning.Plant biotechnology journal · 2026Review
- Adaptive Responses of Tropical Crops: A Multi-Scale Omics Integrated Perspective.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
Prokaryotic genomes are compact and are commonly organised into operons that generate polycistronic transcripts. Plant mitochondrial genomes preserve several prokaryote-like expression features, including frequent polycistronic transcription and extensive post-transcriptional processing. At the same time, frequent rearrangement and recombination in plant mitochondria can create novel open reading frames, some of which cause cytoplasmic male sterility by perturbing mitochondrial function during pollen development. A recurring observation across species is that many sterility-associated open reading frames are co-transcribed in tandem with neighbouring mitochondrial genes, generating characteristic chimeric or extended transcripts that become key targets of nuclear fertility restorer genes. In this review, we synthesise co-transcription patterns of sterility-associated genes in two monocots (rice and maize) and two dicots (oilseed rape and sunflower), and outline how representative restorer genes recognise, cleave, destabilise, or translationally block the corresponding co-transcripts. Building on operon concepts, we discuss how co-transcription may shape transcript abundance, processing, and coupling to retrograde signalling. Finally, we summarise evidence linking sterility gene activity to reactive oxygen species homoeostasis and propose testable hypotheses for how these mitochondrial-nuclear interactions may influence plant adaptation and evolution.
Indexed as
Identifiers
What Socratic 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 Socratic graph.