Evidence map›Paper›PMID 25883242›Full record

ArticlePlant physiology2015

The Apoplastic Copper AMINE OXIDASE1 Mediates Jasmonic Acid-Induced Protoxylem Differentiation in Arabidopsis Roots.

Sandip A Ghuge, Andrea Carucci, Renato A Rodrigues-Pousada, Alessandra Tisi, Stefano Franchi, Paraskevi Tavladoraki, Riccardo Angelini, Alessandra Cona

Open access · greenAbstract read
In one paragraph

Article in Plant physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed, 47 citations in OpenAlex.

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  9. Distinct role of AtCuAOβ- and RBOHD-driven HFrontiers in plant science · 2023
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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 2 institutions in 1 country.

Sandip A GhugeDipartimento di Scienze, Università degli Studi Roma Tre, 00146 Rome, Italy (S.A.G., A.Ca., A.T., S.F., P.T., R.A., A.Co.);Department of Life, Health, and Environmental Sciences, Università dell'Aquila, 67100 L'Aquila, Italy (R.A.R.-P.); andIstituto Nazionale Biostrutture e Biosistemi, 00136 Rome, Italy (P.T., R.A., A.Co.).
Andrea CarucciDipartimento di Scienze, Università degli Studi Roma Tre, 00146 Rome, Italy (S.A.G., A.Ca., A.T., S.F., P.T., R.A., A.Co.);Department of Life, Health, and Environmental Sciences, Università dell'Aquila, 67100 L'Aquila, Italy (R.A.R.-P.); andIstituto Nazionale Biostrutture e Biosistemi, 00136 Rome, Italy (P.T., R.A., A.Co.).
Renato A Rodrigues-PousadaDipartimento di Scienze, Università degli Studi Roma Tre, 00146 Rome, Italy (S.A.G., A.Ca., A.T., S.F., P.T., R.A., A.Co.);Department of Life, Health, and Environmental Sciences, Università dell'Aquila, 67100 L'Aquila, Italy (R.A.R.-P.); andIstituto Nazionale Biostrutture e Biosistemi, 00136 Rome, Italy (P.T., R.A., A.Co.).
Alessandra TisiDipartimento di Scienze, Università degli Studi Roma Tre, 00146 Rome, Italy (S.A.G., A.Ca., A.T., S.F., P.T., R.A., A.Co.);Department of Life, Health, and Environmental Sciences, Università dell'Aquila, 67100 L'Aquila, Italy (R.A.R.-P.); andIstituto Nazionale Biostrutture e Biosistemi, 00136 Rome, Italy (P.T., R.A., A.Co.).
Stefano FranchiDipartimento di Scienze, Università degli Studi Roma Tre, 00146 Rome, Italy (S.A.G., A.Ca., A.T., S.F., P.T., R.A., A.Co.);Department of Life, Health, and Environmental Sciences, Università dell'Aquila, 67100 L'Aquila, Italy (R.A.R.-P.); andIstituto Nazionale Biostrutture e Biosistemi, 00136 Rome, Italy (P.T., R.A., A.Co.).
Paraskevi TavladorakiDipartimento di Scienze, Università degli Studi Roma Tre, 00146 Rome, Italy (S.A.G., A.Ca., A.T., S.F., P.T., R.A., A.Co.);Department of Life, Health, and Environmental Sciences, Università dell'Aquila, 67100 L'Aquila, Italy (R.A.R.-P.); andIstituto Nazionale Biostrutture e Biosistemi, 00136 Rome, Italy (P.T., R.A., A.Co.).
Riccardo AngeliniDipartimento di Scienze, Università degli Studi Roma Tre, 00146 Rome, Italy (S.A.G., A.Ca., A.T., S.F., P.T., R.A., A.Co.);Department of Life, Health, and Environmental Sciences, Università dell'Aquila, 67100 L'Aquila, Italy (R.A.R.-P.); andIstituto Nazionale Biostrutture e Biosistemi, 00136 Rome, Italy (P.T., R.A., A.Co.).ORCID http://orcid.org/0000-0002-1399-1187
Alessandra ConaDipartimento di Scienze, Università degli Studi Roma Tre, 00146 Rome, Italy (S.A.G., A.Ca., A.T., S.F., P.T., R.A., A.Co.);Department of Life, Health, and Environmental Sciences, Università dell'Aquila, 67100 L'Aquila, Italy (R.A.R.-P.); andIstituto Nazionale Biostrutture e Biosistemi, 00136 Rome, Italy (P.T., R.A., A.Co.) alessandra.cona@uniroma3.it.
Roma Tre University · ITUniversity of L'Aquila · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polyamines are involved in key developmental processes and stress responses. Copper amine oxidases oxidize the polyamine putrescine (Put), producing an aldehyde, ammonia, and hydrogen peroxide (H2O2). The Arabidopsis (Arabidopsis thaliana) amine oxidase gene At4g14940 (AtAO1) encodes an apoplastic copper amine oxidase expressed at the early stages of vascular tissue differentiation in roots. Here, its role in root development and xylem differentiation was explored by pharmacological and forward/reverse genetic approaches. Analysis of the AtAO1 expression pattern in roots by a promoter::green fluorescent protein-β-glucuronidase fusion revealed strong gene expression in the protoxylem at the transition, elongation, and maturation zones. Methyl jasmonate (MeJA) induced AtAO1 gene expression in vascular tissues, especially at the transition and elongation zones. Early protoxylem differentiation was observed upon MeJA treatment along with Put level decrease and H2O2 accumulation in wild-type roots, whereas Atao1 loss-of-function mutants were unresponsive to the hormone. The H2O2 scavenger N,N(1)-dimethylthiourea reversed the MeJA-induced early protoxylem differentiation in wild-type seedlings. Likewise, Put, which had no effect on Atao1 mutants, induced early protoxylem differentiation in the wild type, this event being counteracted by N,N(1)-dimethylthiourea treatment. Consistently, AtAO1-overexpressing plants showed lower Put levels and early protoxylem differentiation concurrent with H2O2 accumulation in the root zone where the first protoxylem cells with fully developed secondary wall thickenings are found. These results show that the H2O2 produced via AtAO1-driven Put oxidation plays a role in MeJA signaling leading to early protoxylem differentiation in root.

Indexed as

AcetatesAmine Oxidase (Copper-Containing)ArabidopsisArabidopsis ProteinsCell DifferentiationCopperCyclopentanesGene Expression Regulation, PlantHydrogen PeroxideMutationOxylipinsPlant RootsPlants, Genetically ModifiedPutrescineThioureaXylem1,3-dimethylthioureaAcetatesAmine Oxidase (Copper-Containing)AO1 copper amine oxidase, ArabidopsisArabidopsis ProteinsCopperCyclopentanesHydrogen Peroxidejasmonic acidmethyl jasmonateOxylipinsPutrescineThiourea

Identifiers

PMID25883242
PMCPMC4453780
OpenAlexW1545313758

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.