Evidence map›Paper›PMID 29876699›Full record

ArticleFunctional & integrative genomics2018

Transcriptome profiling of short-term response to chilling stress in tolerant and sensitive Oryza sativa ssp. Japonica seedlings.

Matteo Buti, Marianna Pasquariello, Domenico Ronga, Justyna Anna Milc, Nicola Pecchioni, Viet The Ho, Chiara Pucciariello, Pierdomenico Perata, Enrico Francia

Abstract read
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In one paragraph

Article in Functional & integrative genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Small subunit isoform diversity underlies structural heterogeneity in native plant Rubisco.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

9 authors.

Matteo ButiBIOGEST-SITEIA, University of Modena and Reggio Emilia, Via Amendola, 2 - Pad. Besta, 42122, Reggio Emilia, Italy. matteo.buti@unimore.it.ORCID http://orcid.org/0000-0002-1430-7826
Marianna PasquarielloDepartment of Crop Genetics, John Innes Centre, Norwich, UK.
Domenico RongaBIOGEST-SITEIA, University of Modena and Reggio Emilia, Via Amendola, 2 - Pad. Besta, 42122, Reggio Emilia, Italy.
Justyna Anna MilcBIOGEST-SITEIA, University of Modena and Reggio Emilia, Via Amendola, 2 - Pad. Besta, 42122, Reggio Emilia, Italy.
Nicola PecchioniDepartment of Life Sciences, University of Modena and Reggio Emilia, Reggio Emilia, Italy.
Viet The HoPlantLab, Scuola Superiore Sant'Anna, Pisa, Italy.
Chiara PucciarielloPlantLab, Scuola Superiore Sant'Anna, Pisa, Italy.
Pierdomenico PerataPlantLab, Scuola Superiore Sant'Anna, Pisa, Italy.
Enrico FranciaBIOGEST-SITEIA, University of Modena and Reggio Emilia, Via Amendola, 2 - Pad. Besta, 42122, Reggio Emilia, Italy.

Funding

Progetto AGER, Integrated Genetic And Genomic Approaches For New Italian Rice Breeding Strategies (RISINNOVA) 2010-2369
6 · The paper itself

Abstract

Low temperature is a major factor limiting rice growth and yield, and seedling is one of the developmental stages at which sensitivity to chilling stress is higher. Tolerance to chilling is a complex quantitative trait, so one of the most effective approaches to identify genes and pathways involved is to compare the stress-induced expression changes between tolerant and sensitive genotypes. Phenotypic responses to chilling of 13 Japonica cultivars were evaluated, and Thaibonnet and Volano were selected as sensitive and tolerant genotypes, respectively. To thoroughly profile the short-term response of the two cultivars to chilling, RNA-Seq was performed on Thaibonnet and Volano seedlings after 0 (not stressed), 2, and 10 h at 10 °C. Differential expression analysis revealed that the ICE-DREB1/CBF pathway plays a primary role in chilling tolerance, mainly due to some important transcription factors involved (some of which had never been reported before). Moreover, the expression trends of some genes that were radically different between Thaibonnet and Volano (i.e., calcium-dependent protein kinases OsCDPK21 and OsCDPK23, cytochrome P450 monooxygenase CYP76M8, etc.) suggest their involvement in low temperature tolerance too. Density of differentially expressed genes along rice genome was determined and linked to the position of known QTLs: remarkable co-locations were reported, delivering an overview of genomic regions determinant for low temperature response at seedling stage. Our study contributes to a better understanding of the molecular mechanisms underlying rice response to chilling and provides a solid background for development of low temperature-tolerant germplasm.

Indexed as

Cold-Shock ResponseTranscriptomeGene Expression Regulation, PlantOryzaPlant ProteinsPlant ProteinsChilling toleranceDifferentially expressed genesOryza sativaRNA-SeqShort-term response

Identifiers

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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.