Evidence map›Paper›PMID 25344399›Full record

ArticleRNA (New York, N.Y.)2014

Distinctive profiles of small RNA couple inverted repeat-induced post-transcriptional gene silencing with endogenous RNA silencing pathways in Arabidopsis.

Tadeusz Wroblewski, Marta Matvienko, Urszula Piskurewicz, Huaqin Xu, Belinda Martineau, Joan Wong, Manjula Govindarajulu, Alexander Kozik, Richard W Michelmore

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. The Whys and Wherefores of Transitivity in Plants.Frontiers in plant science · 2020
    Review
  7. Article
  8. PCIR: a database of Plant Chloroplast Inverted Repeats.Database : the journal of biological databases and curation · 2019
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

9 authors at 1 institution in 1 country.

Tadeusz WroblewskiThe Genome Center, University of California, Davis, Davis, California 95616, USA tadeusz.academicus@gmail.com.
Marta MatvienkoThe Genome Center, University of California, Davis, Davis, California 95616, USA.
Urszula PiskurewiczThe Genome Center, University of California, Davis, Davis, California 95616, USA.
Huaqin XuThe Genome Center, University of California, Davis, Davis, California 95616, USA.
Belinda MartineauThe Genome Center, University of California, Davis, Davis, California 95616, USA.
Joan WongThe Genome Center, University of California, Davis, Davis, California 95616, USA.
Manjula GovindarajuluThe Genome Center, University of California, Davis, Davis, California 95616, USA.
Alexander KozikThe Genome Center, University of California, Davis, Davis, California 95616, USA.
Richard W MichelmoreThe Genome Center, University of California, Davis, Davis, California 95616, USA Department of Plant Science, University of California, Davis, Davis, California 95616, USA Department of Molecular and Cellular Biology, University of California, Davis, Davis, California 95616, USA Department of Medical Microbiology and Immunology, University of California, Davis, Davis, California 95616, USA.
University of California, Davis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The experimental induction of RNA silencing in plants often involves expression of transgenes encoding inverted repeat (IR) sequences to produce abundant dsRNAs that are processed into small RNAs (sRNAs). These sRNAs are key mediators of post-transcriptional gene silencing (PTGS) and determine its specificity. Despite its application in agriculture and broad utility in plant research, the mechanism of IR-PTGS is incompletely understood. We generated four sets of 60 Arabidopsis plants, each containing IR transgenes expressing different configurations of uidA and CHALCONE Synthase (At-CHS) gene fragments. Levels of PTGS were found to depend on the orientation and position of the fragment in the IR construct. Deep sequencing and mapping of sRNAs to corresponding transgene-derived and endogenous transcripts identified distinctive patterns of differential sRNA accumulation that revealed similarities among sRNAs associated with IR-PTGS and endogenous sRNAs linked to uncapped mRNA decay. Detailed analyses of poly-A cleavage products from At-CHS mRNA confirmed this hypothesis. We also found unexpected associations between sRNA accumulation and the presence of predicted open reading frames in the trigger sequence. In addition, strong IR-PTGS affected the prevalence of endogenous sRNAs, which has implications for the use of PTGS for experimental or applied purposes.

Indexed as

Gene SilencingRNA InterferenceAcyltransferasesArabidopsisGene Expression Regulation, PlantHigh-Throughput Nucleotide SequencingInverted Repeat SequencesPlants, Genetically ModifiedRNA, Double-StrandedRNA, MessengerRNA, Small InterferingRNA StabilitySignal TransductionAcyltransferasesflavanone synthetaseRNA, Double-StrandedRNA, MessengerRNA, Small Interferingchalcone synthasehairpin RNAheterochromatic siRNARNA decaytransitivitytranslation

Identifiers

PMID25344399
PMCPMC4238362
OpenAlexW2123344312

What OpenQuestion holds

Textmetadata
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.