Evidence map›Paper›PMID 27982722›Full record

ArticleRNA biology2017

TargetLink, a new method for identifying the endogenous target set of a specific microRNA in intact living cells.

Yan Xu, Yan Chen, Daliang Li, Qing Liu, Zhenyu Xuan, Wen-Hong Li

Abstract read
In one paragraph

Article in RNA biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

6 authors.

Yan Xua Department of Cell Biology and of Biochemistry , University of Texas Southwestern Medical Center , Dallas , TX , USA.
Yan Chena Department of Cell Biology and of Biochemistry , University of Texas Southwestern Medical Center , Dallas , TX , USA.
Daliang Lia Department of Cell Biology and of Biochemistry , University of Texas Southwestern Medical Center , Dallas , TX , USA.
Qing Liua Department of Cell Biology and of Biochemistry , University of Texas Southwestern Medical Center , Dallas , TX , USA.
Zhenyu Xuanb Department of Biological Sciences , Center for Systems Biology, The University of Texas at Dallas , Richardson , TX , USA.
Wen-Hong Lia Department of Cell Biology and of Biochemistry , University of Texas Southwestern Medical Center , Dallas , TX , USA.

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Sandi Leigh Pruitt · 2010 to 2026
$53.7M
Photonic probe and techniques for biological imaging applicationsR01GM077593 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI LI, WEN-HONG · 2006 to 2015
$2.7M
NCI NIH HHS P30 CA142543NIGMS NIH HHS R01 GM077593
6 · The paper itself

Abstract

MicroRNAs are small non-coding RNAs acting as posttranscriptional repressors of gene expression. Identifying mRNA targets of a given miRNA remains an outstanding challenge in the field. We have developed a new experimental approach, TargetLink, that applied locked nucleic acid (LNA) as the affinity probe to enrich target genes of a specific microRNA in intact cells. TargetLink also consists a rigorous and systematic data analysis pipeline to identify target genes by comparing LNA-enriched sequences between experimental and control samples. Using miR-21 as a test microRNA, we identified 12 target genes of miR-21 in a human colorectal cancer cell by this approach. The majority of the identified targets interacted with miR-21 via imperfect seed pairing. Target validation confirmed that miR-21 repressed the expression of the identified targets. The cellular abundance of the identified miR-21 target transcripts varied over a wide range, with some targets expressed at a rather low level, confirming that both abundant and rare transcripts are susceptible to regulation by microRNAs, and that TargetLink is an efficient approach for identifying the target set of a specific microRNA in intact cells. C20orf111, one of the novel targets identified by TargetLink, was found to reside in the nuclear speckle and to be reliably repressed by miR-21 through the interaction at its coding sequence.

Indexed as

Gene Expression ProfilingRNA InterferenceBase PairingBase SequenceCell LineGene ExpressionGene Knockout TechniquesGenes, ReporterHigh-Throughput Nucleotide SequencingHumansMicroRNAsOligonucleotidesRNA, Messengerlocked nucleic acidMicroRNAsMIRN21 microRNA, humanOligonucleotidesRNA, MessengerColorectal cancerLNAlocked nucleic acidmicroRNAmicroRNA targetmiR-21target identificationtargetlink

Identifiers

PMID27982722
PMCPMC5324748

What OpenQuestion holds

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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.