Evidence map›Paper›PMID 24926684›Full record

ArticlePloS one2014

Certain adenylated non-coding RNAs, including 5' leader sequences of primary microRNA transcripts, accumulate in mouse cells following depletion of the RNA helicase MTR4.

Jane E Dorweiler, Ting Ni, Jun Zhu, Stephen H Munroe, James T Anderson

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

5 authors at 3 institutions in 1 country.

Jane E DorweilerDepartment of Biological Sciences, Marquette University, Milwaukee, Wisconsin, United States of America.
Ting NiDNA Sequencing and Genomics Core, Genetics and Development Biology Center, National Institutes of Health, National Heart Lung and Blood Institute, Bethesda, Maryland, United States of America.
Jun ZhuDNA Sequencing and Genomics Core, Genetics and Development Biology Center, National Institutes of Health, National Heart Lung and Blood Institute, Bethesda, Maryland, United States of America.
Stephen H MunroeDepartment of Biological Sciences, Marquette University, Milwaukee, Wisconsin, United States of America.
James T AndersonDepartment of Biological Sciences, Marquette University, Milwaukee, Wisconsin, United States of America.
Marquette University · USNational Heart Lung and Blood Institute · USNational Institutes of Health · US

Funding

DNA Sequencing Core (DSC)ZICHL006058 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI ZHU, JUN · 2010 to 2016
$16.6M
Molecular and biochemical probing of yeast, RNA surveillance complex TRAMPR15GM100445 · NIGMS · MARQUETTE UNIVERSITY · PI ANDERSON, JAMES T · 2012 to 2014
$310k
Intramural NIH HHSNIGMS NIH HHS 1R15GM100445-01A1NIGMS NIH HHS R15 GM100445
6 · The paper itself

Abstract

RNA surveillance plays an important role in posttranscriptional regulation. Seminal work in this field has largely focused on yeast as a model system, whereas exploration of RNA surveillance in mammals is only recently begun. The increased transcriptional complexity of mammalian systems provides a wider array of targets for RNA surveillance, and, while many questions remain unanswered, emerging data suggest the nuclear RNA surveillance machinery exhibits increased complexity as well. We have used a small interfering RNA in mouse N2A cells to target the homolog of a yeast protein that functions in RNA surveillance (Mtr4p). We used high-throughput sequencing of polyadenylated RNAs (PA-seq) to quantify the effects of the mMtr4 knockdown (KD) on RNA surveillance. We demonstrate that overall abundance of polyadenylated protein coding mRNAs is not affected, but several targets of RNA surveillance predicted from work in yeast accumulate as adenylated RNAs in the mMtr4KD. microRNAs are an added layer of transcriptional complexity not found in yeast. After Drosha cleavage separates the pre-miRNA from the microRNA's primary transcript, the byproducts of that transcript are generally thought to be degraded. We have identified the 5' leading segments of pri-miRNAs as novel targets of mMtr4 dependent RNA surveillance.

Indexed as

5' Untranslated RegionsAnimalsCell LineGene Knockdown TechniquesHigh-Throughput Nucleotide SequencingMiceMicroRNAsNuclear ProteinsPoly ARibonuclease IIIRNA-Binding ProteinsRNA HelicasesRNA, Small InterferingRNA StabilitySequence Analysis, RNA5' Untranslated RegionsDrosha protein, mouseMicroRNAsNuclear ProteinsPoly ARibonuclease IIIRNA-Binding ProteinsRNA HelicasesRNA, Small InterferingSKIV2L2 protein, mouse

Identifiers

PMID24926684
PMCPMC4057207
OpenAlexW2049015596

What OpenQuestion holds

Textmetadata
LicenceCC0
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.