Evidence map›Paper›PMID 24475369›Full record

ArticleMobile genetic elements2013

Continuing analysis of microRNA origins: Formation from transposable element insertions and noncoding RNA mutations.

Justin T Roberts, Elvera A Cooper, Connor J Favreau, Jacob S Howell, Lee G Lane, James E Mills, Derrick C Newman, Tabitha J Perry, Meaghan E Russell, Brittany M Wallace and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Mobile genetic elements, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 41 citations in OpenAlex.

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  13. The role of Alu elements in the cis-regulation of RNA processing.Cellular and molecular life sciences : CMLS · 2015
    Review
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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

11 authors at 2 institutions in 1 country.

Justin T RobertsDepartment of Biological Sciences, University of South Alabama; Mobile, AL USA.
Elvera A CooperDepartment of Biological Sciences, University of South Alabama; Mobile, AL USA.
Connor J FavreauDepartment of Biological Sciences, University of South Alabama; Mobile, AL USA.
Jacob S HowellDepartment of Biological Sciences, University of South Alabama; Mobile, AL USA.
Lee G LaneDepartment of Biological Sciences, University of South Alabama; Mobile, AL USA.
James E MillsDepartment of Biological Sciences, University of South Alabama; Mobile, AL USA.
Derrick C NewmanDepartment of Biological Sciences, University of South Alabama; Mobile, AL USA.
Tabitha J PerryDepartment of Biological Sciences, University of South Alabama; Mobile, AL USA.
Meaghan E RussellDepartment of Biological Sciences, University of South Alabama; Mobile, AL USA.
Brittany M WallaceDepartment of Biological Sciences, University of South Alabama; Mobile, AL USA.
Glen M BorchertDepartment of Biological Sciences, University of South Alabama; Mobile, AL USA.
University of South Alabama · USUniversity of Mobile · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRs) are small noncoding RNAs that typically act as regulators of gene expression by base pairing with the 3' UTR of messenger RNAs (mRNAs) and either repressing their translation or initiating degradation. As of this writing over 24,500 distinct miRs have been identified, but the functions of the vast majority of these remain undescribed. This paper represents a summary of our in depth analysis of the genomic origins of miR loci, detailing the formation of 1,213 of the 7,321 recently identified miRs and thereby bringing the total number of miR loci with defined molecular origin to 3,605. Interestingly, our analyses also identify evidence for a second, novel mechanism of miR locus generation through describing the formation of 273 miR loci from mutations to other forms of noncoding RNAs. Importantly, several independent investigations of the genomic origins of miR loci have now supported the hypothesis that miR hairpins are formed by the adjacent genomic insertion of two complementary transposable elements (TEs) into opposing strands. While our results agree that subsequent transcription over such TE interfaces leads to the formation of the majority of functional miR loci, we now also find evidence suggesting that a subset of miR loci were actually formed by an alternative mechanism-point mutations in other structurally complex, noncoding RNAs (e.g., tRNAs and snoRNAs).

Indexed as

LINEmicroRNAmiRmiRNAnoncoding RNArepetitiveretrotransposonSINEtransposabletransposon

Identifiers

PMID24475369
PMCPMC3891635
OpenAlexW1579605247

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.