Evidence map›Paper›PMID 39474910›Full record

ArticlePlant physiology2024

Using native and synthetic genes to disrupt inositol pyrophosphates and phosphate accumulation in plants.

Catherine Freed, Branch Craige, Janet Donahue, Caitlin Cridland, Sarah Phoebe Williams, Chris Pereira, Jiwoo Kim, Hannah Blice, James Owen, Glenda Gillaspy

Abstract read
In one paragraph

Article in Plant physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Science advances · 2026
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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

10 authors.

Catherine FreedDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.ORCID 0000-0001-9999-5930
Branch CraigeDepartment of Biochemistry, Virginia Tech, Blacksburg, VA 24061, USA.
Janet DonahueDepartment of Biochemistry, Virginia Tech, Blacksburg, VA 24061, USA.
Caitlin CridlandDepartment of Biochemistry, Virginia Tech, Blacksburg, VA 24061, USA.
Sarah Phoebe WilliamsDepartment of Biology, The College of William & Mary, Williamsburg, VA 23185, USA.
Chris PereiraDepartment of Biochemistry, Virginia Tech, Blacksburg, VA 24061, USA.
Jiwoo KimDepartment of BioSciences, Rice University, Houston, TX 77005, USA.ORCID 0000-0002-2237-1895
Hannah BliceApplication Technology Research Unit, US Department of Agriculture, Agricultural Research Service, Wooster, OH 44691, USA.
James OwenApplication Technology Research Unit, US Department of Agriculture, Agricultural Research Service, Wooster, OH 44691, USA.ORCID 0000-0002-7791-5407
Glenda GillaspyDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.ORCID 0000-0003-0932-8232

Funding

National Institute of Food and AgricultureNational Science Foundation MCB 1616038Virginia Tech Institute for Critical Technologies
6 · The paper itself

Abstract

Inositol pyrophosphates are eukaryotic signaling molecules that have been recently identified as key regulators of plant phosphate sensing and homeostasis. Given the importance of phosphate to current and future agronomic practices, we sought to design plants, which could be used to sequester phosphate, as a step in a phytoremediation strategy. To achieve this, we expressed diadenosine and diphosphoinositol polyphosphate phosphohydrolase (DDP1), a yeast (Saccharomyces cerevisiae) enzyme demonstrated to hydrolyze inositol pyrophosphates, in Arabidopsis thaliana and pennycress (Thlaspi arvense), a spring annual cover crop with emerging importance as a biofuel crop. DDP1 expression in Arabidopsis decreased inositol pyrophosphates, activated phosphate starvation response marker genes, and increased phosphate accumulation. These changes corresponded with alterations in plant growth and sensitivity to exogenously applied phosphate. Pennycress plants expressing DDP1 displayed increases in phosphate accumulation, suggesting that these plants could potentially serve to reclaim phosphate from phosphate-polluted soils. We also identified a native Arabidopsis gene, Nucleoside diphosphate-linked moiety X 13 (NUDIX13), which we show encodes an enzyme homologous to DDP1 with similar substrate specificity. Arabidopsis transgenics overexpressing NUDIX13 had lower inositol pyrophosphate levels and displayed phenotypes similar to DDP1-overexpressing transgenics, while nudix13-1 mutants had increased levels of inositol pyrophosphates. Taken together, our data demonstrate that DDP1 and NUDIX13 can be used in strategies to regulate plant inositol pyrophosphates and could serve as potential targets for engineering plants to reclaim phosphate from polluted environments.

Indexed as

ArabidopsisInositol PhosphatesPhosphatesAcid Anhydride HydrolasesArabidopsis ProteinsGene Expression Regulation, PlantPlants, Genetically ModifiedSaccharomyces cerevisiaeAcid Anhydride HydrolasesArabidopsis Proteinsdiphosphoinositol polyphosphate phosphohydrolaseinositol-1-pyrophosphateInositol PhosphatesPhosphates

Identifiers

PMID39474910
PMCPMC11663554

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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.