ArticleBMC plant biology2026
Whole-plant spatiotemporal responses to salinity reveal osmotic and ionic drivers of salt tolerance in broccoli.
Article in BMC plant biology, 2026. 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
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundSoil salinity is a critical threat to global agriculture and understanding the dynamic and tissue-specific responses of crops exposed to salt is essential for developing mitigation strategies. Broccoli (Brassica oleracea L. var. italica), a crop that shows sensitivity to salinity while retaining the ability to activate adaptive responses, has not been extensively studied at the molecular level under salinity. In this study, we conducted a time-course analysis combining transcriptomic, physiological, and biochemical approaches to unravel the mechanisms underlying the tolerance of broccoli to salt stress.
resultsA time-course analysis combining transcriptomics, physiology, and biochemistry revealed that broccoli employs a highly coordinated systemic strategy. First, osmotic adaptation was driven by rapid and sustained osmoprotection through P5CS activation and PDH1 repression, resulting in robust proline accumulation. Second, ionic stress responses were highly tissue-specific: leaves prioritized early K⁺ homeostasis, while roots acted as primary sensors, triggering early signalling and exclusion via the SOS1/SOS3.1 pathway, NHX1.1/NHX2 vacuolar sequestration, and a robust root-specific induction of the cation/H⁺ exchanger CHX20, highlighting a prioritized mechanism for pH and ionic homeostasis. Last, shoots showed oxidative stress responses via GSTU and AOX genes, complemented by mitochondrial protection in roots. Systemic coordination was further supported by altered hormone and phenylpropanoid profiles, reflected by the late-stage accumulation of chlorogenic acid in leaves to preserve photosynthetic function. This systemic coordination was supported by a complex hormonal redistribution of ABA, JA, and IAA in roots and early SA increases in shoots. Furthermore, salinity complexly regulated secondary metabolism; despite late-stage glucobrassicin declines in leaves, early transcriptomic activation of glucosinolate biosynthesis and differential GTR expression suggested enhanced glucosinolate turnover and redistribution under stress.
conclusionsOur results provide a comprehensive spatiotemporal map of the response of broccoli to salinity, highlighting key candidate genes and physiological traits associated with moderate salinity acclimation, providing a framework to explore strategies for sustaining productivity in saline environments.
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.