Evidence map›Paper›PMID 28087842›Full record

ArticleGenome research2017

Novel determinants of mammalian primary microRNA processing revealed by systematic evaluation of hairpin-containing transcripts and human genetic variation.

Christine Roden, Jonathan Gaillard, Shaveta Kanoria, William Rennie, Syndi Barish, Jijun Cheng, Wen Pan, Jun Liu, Chris Cotsapas, Ye Ding and 1 more

Abstract read
In one paragraph

Article in Genome research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing 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

58 citing papers in PubMed.

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  6. Relationship Between the Occurrence of Depression andInternational journal of molecular sciences · 2024
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Christine RodenDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
Jonathan GaillardYale Stem Cell Center and Yale Cancer Center, Yale University, New Haven, Connecticut 06520, USA.
Shaveta KanoriaWadsworth Center, New York State Department of Health, Albany, New York 12208, USA.
William RennieWadsworth Center, New York State Department of Health, Albany, New York 12208, USA.
Syndi BarishGraduate Program in Biological and Biomedical Sciences, Yale University, New Haven, Connecticut 06510, USA.
Jijun ChengDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
Wen PanDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
Jun LiuDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
Chris CotsapasDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
Ye DingWadsworth Center, New York State Department of Health, Albany, New York 12208, USA.
Jun LuDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

Funding

Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI DAVID L RIMM · 1985 to 2026
$85.0M
GENETICS AND GENOMICS OF HUMAN DISEASET32HD007149 · NICHD · YALE UNIVERSITY · PI James P Noonan · 1985 to 2026
$8.2M
Short Term Research Training: Students in Health Professional SchoolsT35DK104689 · NIDDK · YALE UNIVERSITY · PI LLOYD G CANTLEY, Sarwat I Chaudhry · 2015 to 2026
$2.6M
Novel Approaches to Mammalian MicroRNA Target PredictionR01GM099811 · NIGMS · WADSWORTH CENTER · PI DING, YE, LU, JUN · 2012 to 2015
$2.4M
Quantitative Modeling of MicroRNA:Target Interactions in Cell Fate TransitionR01GM116855 · NIGMS · WADSWORTH CENTER · PI DING, YE, LU, JUN · 2016 to 2019
$2.2M
The role of microRNAs in leukemic initiation and maintenanceR01CA149109 · NCI · YALE UNIVERSITY · PI LU, JUN · 2011 to 2015
$1.7M
NCI NIH HHS P30 CA016359NCI NIH HHS R01 CA149109NICHD NIH HHS T32 HD007149NIDDK NIH HHS T35 DK104689NIGMS NIH HHS R01 GM099811NIGMS NIH HHS R01 GM116855
6 · The paper itself

Abstract

Mature microRNAs (miRNAs) are processed from hairpin-containing primary miRNAs (pri-miRNAs). However, rules that distinguish pri-miRNAs from other hairpin-containing transcripts in the genome are incompletely understood. By developing a computational pipeline to systematically evaluate 30 structural and sequence features of mammalian RNA hairpins, we report several new rules that are preferentially utilized in miRNA hairpins and govern efficient pri-miRNA processing. We propose that a hairpin stem length of 36 ± 3 nt is optimal for pri-miRNA processing. We identify two bulge-depleted regions on the miRNA stem, located ∼16-21 nt and ∼28-32 nt from the base of the stem, that are less tolerant of unpaired bases. We further show that the CNNC primary sequence motif selectively enhances the processing of optimal-length hairpins. We predict that a small but significant fraction of human single-nucleotide polymorphisms (SNPs) alter pri-miRNA processing, and confirm several predictions experimentally including a disease-causing mutation. Our study enhances the rules governing mammalian pri-miRNA processing and suggests a diverse impact of human genetic variation on miRNA biogenesis.

Indexed as

Inverted Repeat SequencesPolymorphism, Single NucleotideRNA Processing, Post-TranscriptionalAnimalsCell LineHumansMiceMicroRNAsMicroRNAs

Identifiers

PMID28087842
PMCPMC5340965

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.