Evidence map›Paper›PMID 25938773›Full record

ArticlePloS one2015

Cold Responsive Gene Expression Profiling of Sugarcane and Saccharum spontaneum with Functional Analysis of a Cold Inducible Saccharum Homolog of NOD26-Like Intrinsic Protein to Salt and Water Stress.

Jong-Won Park, Thiago R Benatti, Thiago Marconi, Qingyi Yu, Nora Solis-Gracia, Victoria Mora, Jorge A da Silva

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
9.3field-weighted citation impact, top 3% 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

19 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
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  6. Article
  7. A Sugarcane G-Protein-Coupled Receptor,Frontiers in plant science · 2021
    Article
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  9. Article
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  12. Review
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  15. Article
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  18. Hormonal control of cold stress responses in plants.Cellular and molecular life sciences : CMLS · 2016
    Review
  19. Review
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

7 authors at 1 institution in 1 country.

Jong-Won ParkTexas A&M AgriLife Research, The Texas A&M System, Weslaco, Texas, United States of America.
Thiago R BenattiTexas A&M AgriLife Research, The Texas A&M System, Weslaco, Texas, United States of America.
Thiago MarconiTexas A&M AgriLife Research, The Texas A&M System, Weslaco, Texas, United States of America.
Qingyi YuTexas A&M AgriLife Research, The Texas A&M System, Dallas, Texas, United States of America.
Nora Solis-GraciaTexas A&M AgriLife Research, The Texas A&M System, Weslaco, Texas, United States of America.
Victoria MoraTexas A&M AgriLife Research, The Texas A&M System, Weslaco, Texas, United States of America.
Jorge A da SilvaTexas A&M AgriLife Research, The Texas A&M System, Weslaco, Texas, United States of America.
Texas A&M University System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transcriptome analysis of sugarcane hybrid CP72-1210 (cold susceptible) and Saccharum spontaneum TUS05-05 (cold tolerant) using Sugarcane Assembled Sequences (SAS) from SUCEST-FUN Database showed that a total of 35,340 and 34,698 SAS genes, respectively, were expressed before and after chilling stress. The analysis revealed that more than 600 genes are differentially expressed in each genotype after chilling stress. Blast2Go annotation revealed that the major difference in gene expression profiles between CP72-1210 and TUS05-05 after chilling stress are present in the genes related to the transmembrane transporter activity. To further investigate the relevance of transmembrane transporter activity against abiotic stress tolerance, a S. spontaneum homolog of a NOD26-like major intrinsic protein gene (SspNIP2) was selected for functional analysis, of which expression was induced after chilling stress in the cold tolerant TUS05-05. Quantitative real-time PCR showed that SspNIP2 expression was increased ~2.5 fold at 30 minutes after cold treatment and stayed induced throughout the 24 hours of cold treatment. The amino acid sequence analysis of the cloned SspNIP2 confirmed the presence of six transmembrane domains and two NPA (Asn-Pro-Ala) motifs, signature features of major intrinsic protein families. Amino acid analysis confirmed that four amino acids, comprising the ar/R (aromatic residue/arginine) region responsible for the substrate specificity among MIPs, are conserved among monocot silicon transporters and SspNIP2. Salinity stress test on SspNIP2 transgenic tobacco plants resulted in more vigorous transgenic lines than the non-transgenic tobacco plants, suggesting some degree of tolerance to salt stress conferred by SspNIP2. SspNIP2-transgenic plants, exposed to 2 weeks of water stress without irrigation, developed various degrees of water stress symptom. The water stress test confirmed that the SspNIP2 transgenic lines had lower evapotranspiration rates than non-transgenic lines, suggesting that SspNIP2 transgenic lines showed a slight tolerance to the early water stress compared to wild type plants.

Indexed as

Gene Expression ProfilingGene Expression Regulation, PlantStress, PhysiologicalTranscriptomeAmino Acid SequenceCloning, MolecularCold TemperatureComputational BiologyHigh-Throughput Nucleotide SequencingMolecular Sequence AnnotationMolecular Sequence DataNicotianaPhenotypePlant ProteinsPlants, Genetically ModifiedSaccharumPlant Proteins

Identifiers

PMID25938773
PMCPMC4418668
OpenAlexW1520029547

What OpenQuestion holds

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LicenceCC BY
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.