Evidence map›Paper›PMID 33787959›Full record

ArticlePlant cell reports2021

Nitrogen inputs influence vegetative metabolism in maize engineered with a seed-specific carotenoid pathway.

Patricia S Girón-Calva, Laura Pérez-Fons, Gerhard Sandmann, Paul D Fraser, Paul Christou

Abstract read
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In one paragraph

Article in Plant cell reports, 2021. 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
0.2field-weighted citation impact, top 58% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
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

5 authors at 4 institutions in 3 countries.

Patricia S Girón-CalvaDepartment of Plant Production and Forestry Sciences, University of Lleida-Agrotecnio Center, Lleida, Spain.ORCID http://orcid.org/0000-0003-0166-8478
Laura Pérez-FonsDepartment of Biological Sciences, Royal Holloway, University London, Egham, Surrey, UK.
Gerhard SandmannInstitute of Molecular Bioscience, J. W. Goethe University, Frankfurt am Main, Germany.
Paul D FraserDepartment of Biological Sciences, Royal Holloway, University London, Egham, Surrey, UK. p.fraser@rhul.ac.uk.
Paul ChristouDepartment of Plant Production and Forestry Sciences, University of Lleida-Agrotecnio Center, Lleida, Spain. paul.christou@udl.cat.ORCID http://orcid.org/0000-0001-6358-7396
Royal Holloway University of London · GBGoethe University Frankfurt · DEInstitució Catalana de Recerca i Estudis Avançats · ESUniversitat de Lleida · ES

Funding

Department for Environment, Food and Rural Affairs CH0217Ministerio de Ciencia, Innovación y Universidades PCI2019-103382
6 · The paper itself

Abstract

key messageMetabolomic profiling of a maize line engineered with an endosperm-specific carotenogenic pathway revealed unexpected metabolic readjustments of primary metabolism in leaves and roots. High-carotenoid (HC) maize was engineered to accumulate high levels of carotenoids in the endosperm. The metabolic interventions influenced the flux through non-target pathways in tissues that were not affected by the targeted intervention. HC maize at the vegetative stage also showed a reduced susceptibility to insect feeding. It is unknown, however, whether the metabolic history of the embryo has any impact on the metabolite composition in vegetative tissues. We, therefore, compared HC maize and its isogenic counterpart (M37W) to test the hypothesis that boosting the carotenoid content in the endosperm triggers compensatory effects in core metabolism in vegetative tissues. Specifically, we investigated whether the metabolite composition of leaves and roots at the V6 stage differs between HC and M37W, and whether N inputs further alter the core metabolism of HC compared to M37W. We found an increase in the abundance of organic acids from the tricarboxylic acid (TCA) cycle in HC even under restricted N conditions. In contrast, low levels of carotenoids and chlorophyll were measured regardless of N levels. Sugars were also significantly depleted in HC under low N. We propose a model explaining the observed genotype-dependent and input-dependent effects, in which organic acids derived from the TCA cycle accumulate during vegetative growth and contribute to the increased demand for pyruvate and/or acetyl-CoA in the endosperm and embryo. This response may in part reflect the transgenerational priming of vegetative tissues in the embryo induced by the increased demand for metabolic precursors during seed development in the previous generation.

Indexed as

Gene Expression Regulation, PlantNitrogenPlants, Genetically ModifiedZea maysNitrogenCarotenoidsMetabolic engineeringNitrogen deprivationTransgenerational primingZea mays

Identifiers

PMID33787959
OpenAlexW3146866198

What OpenQuestion holds

Textmetadata
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.