Evidence map›Paper›PMID 27776116›Full record

ArticleNature genetics2016

General rules for functional microRNA targeting.

Doyeon Kim, You Me Sung, Jinman Park, Sukjun Kim, Jongkyu Kim, Junhee Park, Haeok Ha, Jung Yoon Bae, SoHui Kim, Daehyun Baek

Abstract read
PubMed Publisher
In one paragraph

Article in Nature genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing 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

79 citing papers in PubMed.

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19 more citing papers are in PubMed but not listed here.

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

10 authors.

Doyeon KimCenter for RNA Research, Institute for Basic Science, Seoul, Republic of Korea.
You Me SungSchool of Biological Sciences, Seoul National University, Seoul, Republic of Korea.
Jinman ParkCenter for RNA Research, Institute for Basic Science, Seoul, Republic of Korea.
Sukjun KimCenter for RNA Research, Institute for Basic Science, Seoul, Republic of Korea.
Jongkyu KimCenter for RNA Research, Institute for Basic Science, Seoul, Republic of Korea.
Junhee ParkSchool of Biological Sciences, Seoul National University, Seoul, Republic of Korea.
Haeok HaSchool of Biological Sciences, Seoul National University, Seoul, Republic of Korea.
Jung Yoon BaeSchool of Biological Sciences, Seoul National University, Seoul, Republic of Korea.
SoHui KimCenter for RNA Research, Institute for Basic Science, Seoul, Republic of Korea.
Daehyun BaekCenter for RNA Research, Institute for Basic Science, Seoul, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The functional rules for microRNA (miRNA) targeting remain controversial despite their biological importance because only a small fraction of distinct interactions, called site types, have been examined among an astronomical number of site types that can occur between miRNAs and their target mRNAs. To systematically discover functional site types and to evaluate the contradicting rules reported previously, we used large-scale transcriptome data and statistically examined whether each of approximately 2 billion site types is enriched in differentially downregulated mRNAs responding to overexpressed miRNAs. Accordingly, we identified seven non-canonical functional site types, most of which are novel, in addition to four canonical site types, while also removing numerous false positives reported by previous studies. Extensive experimental validation and significantly elevated 3' UTR sequence conservation indicate that these non-canonical site types may have biologically relevant roles. Our expanded catalog of functional site types suggests that the gene regulatory network controlled by miRNAs may be far more complex than currently understood.

Indexed as

Gene Expression RegulationGene Regulatory Networks3' Untranslated RegionsBinding SitesComputational BiologyGene Expression ProfilingHumansMicroRNAsRNA, Messenger3' Untranslated RegionsMicroRNAsRNA, Messenger

Identifiers

PMID27776116

What OpenQuestion holds

Textmetadata
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Registered trials

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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.