Evidence map›Paper›PMID 26662272›Full record

ArticlePlant physiology2016

Phloem-Specific Methionine Recycling Fuels Polyamine Biosynthesis in a Sulfur-Dependent Manner and Promotes Flower and Seed Development.

Wolfgang Zierer, Mohammad R Hajirezaei, Kai Eggert, Norbert Sauer, Nicolaus von Wirén, Benjamin Pommerrenig

Open access · hybridAbstract read
In one paragraph

Article in Plant physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Effect of Ethephon on Ethylene and Chlorophyll inInternational journal of molecular sciences · 2024
    Article
  5. Article
  6. Exogenous spermidine improved drought tolerance inFrontiers in plant science · 2023
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. MiR319 mediated salt tolerance by ethylene.Plant biotechnology journal · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Metabolic Investigation ofFrontiers in plant science · 2017
    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

6 authors at 2 institutions in 1 country.

Wolfgang ZiererFriedrich-Alexander-Universität Erlangen-Nürnberg, Department of Biology, Molecular Plant Physiology, 91058 Erlangen, Germany (W.Z., N.S.); andMolecular Plant Nutrition (M.R.H., K.E., N.v.W.) and Metalloid Transport (B.P.), Department of Physiology and Cell Biology, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), 06466 Gatersleben, Germany.ORCID http://orcid.org/0000-0002-0397-8296
Mohammad R HajirezaeiFriedrich-Alexander-Universität Erlangen-Nürnberg, Department of Biology, Molecular Plant Physiology, 91058 Erlangen, Germany (W.Z., N.S.); andMolecular Plant Nutrition (M.R.H., K.E., N.v.W.) and Metalloid Transport (B.P.), Department of Physiology and Cell Biology, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), 06466 Gatersleben, Germany.
Kai EggertFriedrich-Alexander-Universität Erlangen-Nürnberg, Department of Biology, Molecular Plant Physiology, 91058 Erlangen, Germany (W.Z., N.S.); andMolecular Plant Nutrition (M.R.H., K.E., N.v.W.) and Metalloid Transport (B.P.), Department of Physiology and Cell Biology, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), 06466 Gatersleben, Germany.ORCID http://orcid.org/0000-0003-1540-4086
Norbert SauerFriedrich-Alexander-Universität Erlangen-Nürnberg, Department of Biology, Molecular Plant Physiology, 91058 Erlangen, Germany (W.Z., N.S.); andMolecular Plant Nutrition (M.R.H., K.E., N.v.W.) and Metalloid Transport (B.P.), Department of Physiology and Cell Biology, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), 06466 Gatersleben, Germany.ORCID http://orcid.org/0000-0003-4357-2079
Nicolaus von WirénFriedrich-Alexander-Universität Erlangen-Nürnberg, Department of Biology, Molecular Plant Physiology, 91058 Erlangen, Germany (W.Z., N.S.); andMolecular Plant Nutrition (M.R.H., K.E., N.v.W.) and Metalloid Transport (B.P.), Department of Physiology and Cell Biology, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), 06466 Gatersleben, Germany.ORCID http://orcid.org/0000-0002-4966-425X
Benjamin PommerrenigFriedrich-Alexander-Universität Erlangen-Nürnberg, Department of Biology, Molecular Plant Physiology, 91058 Erlangen, Germany (W.Z., N.S.); andMolecular Plant Nutrition (M.R.H., K.E., N.v.W.) and Metalloid Transport (B.P.), Department of Physiology and Cell Biology, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), 06466 Gatersleben, Germany pommerrenig@ipk-gatersleben.de.ORCID http://orcid.org/0000-0002-7522-7942
Leibniz-Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK) · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Yang or Met Cycle is a series of reactions catalyzing the recycling of the sulfur (S) compound 5'-methylthioadenosine (MTA) to Met. MTA is produced as a by-product in ethylene, nicotianamine, and polyamine biosynthesis. Whether the Met Cycle preferentially fuels one of these pathways in a S-dependent manner remained unclear so far. We analyzed Arabidopsis (Arabidopsis thaliana) mutants with defects in the Met Cycle enzymes 5-METHYLTHIORIBOSE-1-PHOSPHATE-ISOMERASE1 (MTI1) and DEHYDRATASE-ENOLASE-PHOSPHATASE-COMPLEX1 (DEP1) under different S conditions and assayed the contribution of the Met Cycle to the regeneration of S for these pathways. Neither mti1 nor dep1 mutants could recycle MTA but showed S-dependent reproductive failure, which was accompanied by reduced levels of the polyamines putrescine, spermidine, and spermine in mutant inflorescences. Complementation experiments with external application of these three polyamines showed that only the triamine spermine could specifically rescue the S-dependent reproductive defects of the mutant plants. Furthermore, expressing gene-reporter fusions in Arabidopsis showed that MTI1 and DEP1 were mainly expressed in the vasculature of all plant parts. Phloem-specific reconstitution of Met Cycle activity in mti1 and dep1 mutant plants was sufficient to rescue their S-dependent mutant phenotypes. We conclude from these analyses that phloem-specific S recycling during periods of S starvation is essential for the biosynthesis of polyamines required for flowering and seed development.

Indexed as

Aldose-Ketose IsomerasesArabidopsisArabidopsis ProteinsDeoxyadenosinesEthylenesFlowersMethionineMutationOrgan SpecificityPhloemPlant Growth RegulatorsPolyaminesPutrescineSeedsSpermidineSpermine5'-methylthioadenosine5-methylthioribose5-methylthioribose-1-phosphate isomerase1, ArabidopsisAldose-Ketose IsomerasesArabidopsis ProteinsDeoxyadenosinesethyleneEthylenesMethioninePlant Growth RegulatorsPolyaminesPutrescineSpermidineSpermineSulfurThioglycosidesThionucleosides

Identifiers

PMID26662272
PMCPMC4734553
OpenAlexW2194761599

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.