Evidence map›Paper›PMID 25844118›Full record

ArticleRice (New York, N.Y.)2015

Abiotic stress and genome dynamics: specific genes and transposable elements response to iron excess in rice.

Taciane Finatto, Antonio Costa de Oliveira, Cristian Chaparro, Luciano C da Maia, Daniel R Farias, Leomar G Woyann, Claudete C Mistura, Adriana P Soares-Bresolin, Christel Llauro, Olivier Panaud and 1 more

Abstract read
In one paragraph

Article in Rice (New York, N.Y.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
–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

44 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  5. Ferroptosis in plant immunity.Plant communications · 2025
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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

11 authors.

Taciane FinattoPlant Genomics and Breeding Center, Eliseu Maciel School of Agronomy, Federal University of Pelotas, 96010-610 Pelotas, RS Brazil ; Present address: Universidade Tecnológica Federal do Paraná, Campus Pato Branco, 85503-390 Pato Branco, PR Brazil.
Antonio Costa de OliveiraPlant Genomics and Breeding Center, Eliseu Maciel School of Agronomy, Federal University of Pelotas, 96010-610 Pelotas, RS Brazil.
Cristian ChaparroLaboratoire Génome et Développement des Plantes, UMR 5096, Université de Perpignan Via Domitia, F-66860 Perpignan, France ; CNRS, Laboratoire Génome et Développement des Plantes, UMR 5096, F-66860 Perpignan, France ; Present address: Laboratoire Ecologie et Evolution des Interactions, UMR 5244, F-66860, Université de Perpignan Via Domitia, Perpignan, France.
Luciano C da MaiaPlant Genomics and Breeding Center, Eliseu Maciel School of Agronomy, Federal University of Pelotas, 96010-610 Pelotas, RS Brazil.
Daniel R FariasPlant Genomics and Breeding Center, Eliseu Maciel School of Agronomy, Federal University of Pelotas, 96010-610 Pelotas, RS Brazil.
Leomar G WoyannPlant Genomics and Breeding Center, Eliseu Maciel School of Agronomy, Federal University of Pelotas, 96010-610 Pelotas, RS Brazil.
Claudete C MisturaPlant Genomics and Breeding Center, Eliseu Maciel School of Agronomy, Federal University of Pelotas, 96010-610 Pelotas, RS Brazil.
Adriana P Soares-BresolinPlant Genomics and Breeding Center, Eliseu Maciel School of Agronomy, Federal University of Pelotas, 96010-610 Pelotas, RS Brazil.
Christel LlauroLaboratoire Génome et Développement des Plantes, UMR 5096, Université de Perpignan Via Domitia, F-66860 Perpignan, France ; CNRS, Laboratoire Génome et Développement des Plantes, UMR 5096, F-66860 Perpignan, France.
Olivier PanaudLaboratoire Génome et Développement des Plantes, UMR 5096, Université de Perpignan Via Domitia, F-66860 Perpignan, France ; CNRS, Laboratoire Génome et Développement des Plantes, UMR 5096, F-66860 Perpignan, France.
Nathalie PicaultLaboratoire Génome et Développement des Plantes, UMR 5096, Université de Perpignan Via Domitia, F-66860 Perpignan, France ; CNRS, Laboratoire Génome et Développement des Plantes, UMR 5096, F-66860 Perpignan, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIron toxicity is a root related abiotic stress, occurring frequently in flooded soils. It can affect the yield of rice in lowland production systems. This toxicity is associated with high concentrations of reduced iron (Fe(2+)) in the soil solution. Although the first interface of the element is in the roots, the consequences of an excessive uptake can be observed in several rice tissues. In an original attempt to find both genes and transposable elements involved in the response to an iron toxicity stress, we used a microarray approach to study the transcriptional responses of rice leaves of cv. Nipponbare (Oryza sativa L. ssp. japonica) to iron excess in nutrient solution.

resultsA large number of genes were significantly up- or down-regulated in leaves under the treatment. We analyzed the gene ontology and metabolic pathways of genes involved in the response to this stress and the cis-regulatory elements (CREs) present in the promoter region of up-regulated genes. The majority of genes act in the pathways of lipid metabolic process, carbohydrate metabolism, biosynthesis of secondary metabolites and plant hormones. We also found genes involved in iron acquisition and mobilization, transport of cations and regulatory mechanisms for iron responses, and in oxidative stress and reactive oxygen species detoxification. Promoter regions of 27% of genes up-regulated present at least one significant occurrence of an ABA-responsive CRE. Furthermore, and for the first time, we were able to show that iron stress triggers the up-regulation of many LTR-retrotransposons. We have established a complete inventory of transposable elements transcriptionally activated under iron excess and the CREs which are present in their LTRs.

conclusionThe short-term response of Nipponbare seedlings to iron excess, includes activation of genes involved in iron homeostasis, in particular transporters, transcription factors and ROS detoxification in the leaves, but also many transposable elements. Our data led to the identification of CREs which are associated with both genes and LTR-retrotransposons up-regulated under iron excess. Our results strengthen the idea that LTR-retrotransposons participate in the transcriptional response to stress and could thus confer an adaptive advantage for the plant.

Indexed as

cis-regulatory elementsIron toxicityLTR-retrotransposonMicroarrayRice

Identifiers

PMID25844118
PMCPMC4385019

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Registered trials

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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.