Evidence map›Paper›PMID 37996547›Full record

ArticleScientific reports2023

Tripogon loliiformis tolerates rapid desiccation after metabolic and transcriptional priming during initial drying.

Pauline A Okemo, Isaac Njaci, Young-Mo Kim, Ryan S McClure, Matthew J Peterson, Alexander S Beliaev, Kim K Hixson, Sagadevan Mundree, Brett Williams

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

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.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Pauline A OkemoSchool of Biology and Environmental Science, Queensland University of Technology, Brisbane, QLD, Australia.
Isaac NjaciSchool of Biology and Environmental Science, Queensland University of Technology, Brisbane, QLD, Australia.
Young-Mo KimEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Ryan S McClureEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Matthew J PetersonBiosphere 2, The University of Arizona, Oracle, AZ, USA.
Alexander S BeliaevCentre for Agriculture and the Bioeconomy, Queensland University of Technology, Brisbane, QLD, Australia.
Kim K HixsonEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA.
Sagadevan MundreeSchool of Biology and Environmental Science, Queensland University of Technology, Brisbane, QLD, Australia.
Brett WilliamsSchool of Biology and Environmental Science, Queensland University of Technology, Brisbane, QLD, Australia. b.williams@qut.edu.au.

Funding

Department of Science, Information Technology and Innovation, Queensland Government AQRF04016-17RD2U.S. Department of Energy DE-SC0014081
6 · The paper itself

Abstract

Crop plants and undomesticated resilient species employ different strategies to regulate their energy resources and growth. Most crop species are sensitive to stress and prioritise rapid growth to maximise yield or biomass production. In contrast, resilient plants grow slowly, are small, and allocate their resources for survival in challenging environments. One small group of plants, termed resurrection plants, survive desiccation of their vegetative tissue and regain full metabolic activity upon watering. However, the precise molecular mechanisms underlying this extreme tolerance remain unknown. In this study, we employed a transcriptomics and metabolomics approach, to investigate the mechanisms of desiccation tolerance in Tripogon loliiformis, a modified desiccation-tolerant plant, that survives gradual but not rapid drying. We show that T. loliiformis can survive rapid desiccation if it is gradually dried to 60% relative water content (RWC). Furthermore, the gene expression data showed that T. loliiformis is genetically predisposed for desiccation in the hydrated state, as evidenced by the accumulation of MYB, NAC, bZIP, WRKY transcription factors along with the phytohormones, abscisic acid, salicylic acid, amino acids (e.g., proline) and TCA cycle sugars during initial drying. Through network analysis of co-expressed genes, we observed differential responses to desiccation between T. loliiformis shoots and roots. Dehydrating shoots displayed global transcriptional changes across broad functional categories, although no enrichment was observed during drying. In contrast, dehydrating roots showed distinct network changes with the most significant differences occurring at 40% RWC. The cumulative effects of the early stress responses may indicate the minimum requirements of desiccation tolerance and enable T. loliiformis to survive rapid drying. These findings potentially hold promise for identifying biotechnological solutions aimed at developing drought-tolerant crops without growth and yield penalties.

Indexed as

Adaptation, PhysiologicalDesiccationPlantsPoaceaeWaterWater

Identifiers

PMID37996547
PMCPMC10667271

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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.