Evidence map›Paper›PMID 28403831›Full record

ArticleBMC plant biology2017

The role of Tre6P and SnRK1 in maize early kernel development and events leading to stress-induced kernel abortion.

Samuel W Bledsoe, Clémence Henry, Cara A Griffiths, Matthew J Paul, Regina Feil, John E Lunn, Mark Stitt, L Mark Lagrimini

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
12.7field-weighted citation impact, top 2% of its field
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

30 citing papers in PubMed, 70 citations in OpenAlex.

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  19. Increasing yield on dry fields: molecular pathways with growing potential.The Plant journal : for cell and molecular biology · 2022
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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

8 authors at 5 institutions in 4 countries.

Samuel W BledsoeEAG Laboratories, 4780 Discovery Drive, Columbia, MO, 65201, USA.
Clémence HenryHawkesbury Institute for the Environment, Western Sydney University, Locked Bag 1797, Penrith, NSW, 2751, Australia.
Cara A GriffithsRothamsted Research, West Common, Harpenden, Hertfordshire, AL5 2JQ, UK.
Matthew J PaulRothamsted Research, West Common, Harpenden, Hertfordshire, AL5 2JQ, UK.
Regina FeilMax Planck Institut fϋr Moleckulare Pflanzenphysiologie, Potsdam (OT) Golm, Germany.
John E LunnMax Planck Institut fϋr Moleckulare Pflanzenphysiologie, Potsdam (OT) Golm, Germany.
Mark StittMax Planck Institut fϋr Moleckulare Pflanzenphysiologie, Potsdam (OT) Golm, Germany.
L Mark LagriminiDepartment of Agronomy and Horticulture, University of Nebraska-Lincoln, 377I Plant Science, Lincoln, NE, 68583-0915, USA. mlagrimini2@unl.edu.
Max Planck Institute of Molecular Plant Physiology · DERothamsted Research · GBDiscovery Laboratories (United States) · USUniversity of Nebraska–Lincoln · USWestern Sydney University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDrought stress during flowering is a major contributor to yield loss in maize. Genetic and biotechnological improvement in yield sustainability requires an understanding of the mechanisms underpinning yield loss. Sucrose starvation has been proposed as the cause for kernel abortion; however, potential targets for genetic improvement have not been identified. Field and greenhouse drought studies with maize are expensive and it can be difficult to reproduce results; therefore, an in vitro kernel culture method is presented as a proxy for drought stress occurring at the time of flowering in maize (3 days after pollination). This method is used to focus on the effects of drought on kernel metabolism, and the role of trehalose 6-phosphate (Tre6P) and the sucrose non-fermenting-1-related kinase (SnRK1) as potential regulators of this response.

resultsA precipitous drop in Tre6P is observed during the first two hours after removing the kernels from the plant, and the resulting changes in transcript abundance are indicative of an activation of SnRK1, and an immediate shift from anabolism to catabolism. Once Tre6P levels are depleted to below 1 nmol∙g

conclusionsThe impact of kernel excision from the ear triggers a cascade of events starting with the precipitous drop in Tre6P levels. It is proposed that the removal of Tre6P suppression of SnRK1 activity results in transcription of putative SnRK1 target genes, and the metabolic transition from biosynthesis to catabolism. This highlights the importance of Tre6P in the metabolic response to starvation. We also present evidence that sugars can mediate the activation of SnRK1. The precipitous drop in Tre6P corresponds to a large increase in transcription of ZmTPPA.3, indicating that this specific enzyme may be responsible for the de-phosphorylation of Tre6P. The high levels of Tre6P in the immature embryo are likely important for preventing kernel abortion.

Indexed as

Gene Expression Regulation, PlantMetabolomeModels, BiologicalPlant ProteinsProtein Serine-Threonine KinasesReal-Time Polymerase Chain ReactionRNA, MessengerSeedsStress, PhysiologicalSucroseSugar PhosphatesTrehaloseZea maysPlant ProteinsProtein Serine-Threonine KinasesRNA, MessengerSNF1-related protein kinasesSucroseSugar PhosphatesTrehalosetrehalose-6-phosphatedroughtkernel cultureMaizeSnRK1starvationsugar metabolismtrehalose-6-phosphate

Identifiers

PMID28403831
PMCPMC5389189
OpenAlexW2605547187

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.