Evidence map›Paper›PMID 27385819›Full record

ArticlePlant physiology2016

Salt Stress Reveals a New Role for ARGONAUTE1 in miRNA Biogenesis at the Transcriptional and Posttranscriptional Levels.

Jakub Dolata, Mateusz Bajczyk, Dawid Bielewicz, Katarzyna Niedojadlo, Janusz Niedojadlo, Halina Pietrykowska, Weronika Walczak, Zofia Szweykowska-Kulinska, Artur Jarmolowski

Open access · hybridAbstract read
In one paragraph

Article in Plant physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
20.6field-weighted citation impact, top 1% 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

42 citing papers in PubMed, 90 citations in OpenAlex.

  1. Article
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  6. RNA interference shapes stress responses inFrontiers in plant science · 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

9 authors at 2 institutions in 1 country.

Jakub DolataDepartment of Gene Expression, Faculty of Biology, Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, 61-614 Poznan, Poland (J.D., M.B., D.B., H.P., W.W., Z.S.-K., A.J.); andDepartment of Cell Biology, Faculty of Biology and Environment Protection, Nicolaus Copernicus University, 87-100 Torun, Poland (K.N., J.N.).ORCID 0000-0001-6141-8863
Mateusz BajczykDepartment of Gene Expression, Faculty of Biology, Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, 61-614 Poznan, Poland (J.D., M.B., D.B., H.P., W.W., Z.S.-K., A.J.); andDepartment of Cell Biology, Faculty of Biology and Environment Protection, Nicolaus Copernicus University, 87-100 Torun, Poland (K.N., J.N.).ORCID 0000-0001-7043-2827
Dawid BielewiczDepartment of Gene Expression, Faculty of Biology, Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, 61-614 Poznan, Poland (J.D., M.B., D.B., H.P., W.W., Z.S.-K., A.J.); andDepartment of Cell Biology, Faculty of Biology and Environment Protection, Nicolaus Copernicus University, 87-100 Torun, Poland (K.N., J.N.).ORCID 0000-0002-4322-0746
Katarzyna NiedojadloDepartment of Gene Expression, Faculty of Biology, Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, 61-614 Poznan, Poland (J.D., M.B., D.B., H.P., W.W., Z.S.-K., A.J.); andDepartment of Cell Biology, Faculty of Biology and Environment Protection, Nicolaus Copernicus University, 87-100 Torun, Poland (K.N., J.N.).
Janusz NiedojadloDepartment of Gene Expression, Faculty of Biology, Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, 61-614 Poznan, Poland (J.D., M.B., D.B., H.P., W.W., Z.S.-K., A.J.); andDepartment of Cell Biology, Faculty of Biology and Environment Protection, Nicolaus Copernicus University, 87-100 Torun, Poland (K.N., J.N.).
Halina PietrykowskaDepartment of Gene Expression, Faculty of Biology, Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, 61-614 Poznan, Poland (J.D., M.B., D.B., H.P., W.W., Z.S.-K., A.J.); andDepartment of Cell Biology, Faculty of Biology and Environment Protection, Nicolaus Copernicus University, 87-100 Torun, Poland (K.N., J.N.).ORCID 0000-0003-0524-8067
Weronika WalczakDepartment of Gene Expression, Faculty of Biology, Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, 61-614 Poznan, Poland (J.D., M.B., D.B., H.P., W.W., Z.S.-K., A.J.); andDepartment of Cell Biology, Faculty of Biology and Environment Protection, Nicolaus Copernicus University, 87-100 Torun, Poland (K.N., J.N.).
Zofia Szweykowska-KulinskaDepartment of Gene Expression, Faculty of Biology, Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, 61-614 Poznan, Poland (J.D., M.B., D.B., H.P., W.W., Z.S.-K., A.J.); andDepartment of Cell Biology, Faculty of Biology and Environment Protection, Nicolaus Copernicus University, 87-100 Torun, Poland (K.N., J.N.) artjarmo@amu.edu.pl zofszwey@amu.edu.pl.
Artur JarmolowskiDepartment of Gene Expression, Faculty of Biology, Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, 61-614 Poznan, Poland (J.D., M.B., D.B., H.P., W.W., Z.S.-K., A.J.); andDepartment of Cell Biology, Faculty of Biology and Environment Protection, Nicolaus Copernicus University, 87-100 Torun, Poland (K.N., J.N.) artjarmo@amu.edu.pl zofszwey@amu.edu.pl.
Adam Mickiewicz University in Poznań · PLNicolaus Copernicus University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plants as sessile organisms have developed prompt response mechanisms to react to rapid environmental changes. In addition to the transcriptional regulation of gene expression, microRNAs (miRNAs) are key posttranscriptional regulators of the plant stress response. We show here that the expression levels of many miRNAs were regulated under salt stress conditions. This regulation occurred at the transcriptional and posttranscriptional levels. During salinity stress, the levels of miRNA161 and miRNA173 increased, while the expression of pri-miRNA161 and pri-miRNA173 was down-regulated. Under salt stress conditions, miRNA161 and miRNA173 were stabilized in the cytoplasm, and the expressions of MIR161 and MIR173 were negatively regulated in the nucleus. ARGONAUTE1 (AGO1) participated in both processes. We demonstrated that AGO1 cotranscriptionally controlled the expression of MIR161 and MIR173 in the nucleus. Our results suggests that AGO1 interacts with chromatin at MIR161 and MIR173 loci and causes the disassembly of the transcriptional complex, releasing short and unpolyadenylated transcripts.

Indexed as

Stress, PhysiologicalArabidopsisArabidopsis ProteinsArgonaute ProteinsBlotting, WesternCell NucleusDown-RegulationGene Expression Regulation, PlantMicroRNAsPlants, Genetically ModifiedReverse Transcriptase Polymerase Chain ReactionRNA, PlantRNA StabilitySalinitySodium ChlorideAGO1 protein, ArabidopsisArabidopsis ProteinsArgonaute ProteinsMicroRNAsMIRN161 microRNA, ArabidopsisMIRN173 microRNA, ArabidopsisRNA, PlantSodium Chloride

Identifiers

PMID27385819
PMCPMC5074614
OpenAlexW2461887598

What OpenQuestion holds

Textmetadata
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.