Evidence map›Paper›PMID 25480817›Full record

ArticleRNA (New York, N.Y.)2015

Stress-induced endogenous siRNAs targeting regulatory intron sequences in Brachypodium.

Hsiao-Lin V Wang, Brandon L Dinwiddie, Herman Lee, Julia A Chekanova

Open access · bronzeAbstract read
In one paragraph

Article in RNA (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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Comparative Analysis of Transcriptome and sRNAs Expression Patterns in theInternational journal of molecular sciences · 2021
    Article
  3. International journal of molecular sciences · 2020
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. 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

4 authors at 1 institution in 1 country.

Hsiao-Lin V WangSchool of Biological Sciences, University of Missouri-Kansas City, Kansas City, Missouri 64110, USA.
Brandon L DinwiddieSchool of Biological Sciences, University of Missouri-Kansas City, Kansas City, Missouri 64110, USA.
Herman LeeSchool of Biological Sciences, University of Missouri-Kansas City, Kansas City, Missouri 64110, USA.
Julia A ChekanovaSchool of Biological Sciences, University of Missouri-Kansas City, Kansas City, Missouri 64110, USA chekanovaj@gmail.com.
University of Missouri–Kansas City · US

Funding

Role of the S. cerevisiae Pab1p in mRNA biogenesisR01GM073872 · NIGMS · UNIVERSITY OF MISSOURI KANSAS CITY · PI CHEKANOVA, JULIA A · 2006 to 2009
$1.0M
NIGMS NIH HHS GM073872NIGMS NIH HHS R01 GM073872
6 · The paper itself

Abstract

Exposure to abiotic stresses triggers global changes in the expression of thousands of eukaryotic genes at the transcriptional and post-transcriptional levels. Small RNA (smRNA) pathways and splicing both function as crucial mechanisms regulating stress-responsive gene expression. However, examples of smRNAs regulating gene expression remain largely limited to effects on mRNA stability, translation, and epigenetic regulation. Also, our understanding of the networks controlling plant gene expression in response to environmental changes, and examples of these regulatory pathways intersecting, remains limited. Here, to investigate the role of smRNAs in stress responses we examined smRNA transcriptomes of Brachypodium distachyon plants subjected to various abiotic stresses. We found that exposure to different abiotic stresses specifically induced a group of novel, endogenous small interfering RNAs (stress-induced, UTR-derived siRNAs, or sutr-siRNAs) that originate from the 3' UTRs of a subset of coding genes. Our bioinformatics analyses predicted that sutr-siRNAs have potential regulatory functions and that over 90% of sutr-siRNAs target intronic regions of many mRNAs in trans. Importantly, a subgroup of these sutr-siRNAs target the important intron regulatory regions, such as branch point sequences, that could affect splicing. Our study indicates that in Brachypodium, sutr-siRNAs may affect splicing by masking or changing accessibility of specific cis-elements through base-pairing interactions to mediate gene expression in response to stresses. We hypothesize that this mode of regulation of gene expression may also serve as a general mechanism for regulation of gene expression in plants and potentially in other eukaryotes.

Indexed as

Gene Expression Regulation, PlantTranscriptome3' Untranslated RegionsAdaptation, PhysiologicalBase SequenceBrachypodiumConsensus SequenceGenes, PlantIntronsMolecular Sequence DataPlant ProteinsRegulatory Sequences, Nucleic AcidRNA InterferenceRNA, PlantRNA, Small InterferingStress, Physiological3' Untranslated RegionsPlant ProteinsRNA, PlantRNA, Small Interferingabiotic stressesBrachypodiumsmRNAssplicingsplicing regulation

Identifiers

PMID25480817
PMCPMC4338343
OpenAlexW2126325893

What OpenQuestion holds

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LicenceCC BY-NC
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.