Evidence map›Paper›PMID 23085579›Full record

ArticleRNA biology2012

Novel upstream and downstream sequence elements contribute to polyadenylation efficiency.

Sarah K Darmon, Carol S Lutz

Open access · bronzeAbstract read
In one paragraph

Article in RNA biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

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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

2 authors at 2 institutions in 1 country.

Sarah K DarmonDepartment of Biochemistry and Molecular Biology, UMDNJ-New Jersey Medical School, and the Graduate School of Biomedical Sciences, Newark, NJ, USA.
Carol S Lutz
Rutgers New Jersey Medical SchoolRutgers, The State University of New Jersey · US

Funding

Computational and Experimental Analysis of RNA structures in mRNA polyadenylationR21HG005129 · NHGRI · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI LUTZ, CAROL S, TIAN, BIN · 2009 to 2010
$429k
NHGRI NIH HHS 1R21HG005129-01NHGRI NIH HHS R21 HG005129
6 · The paper itself

Abstract

Polyadenylation is a 3' mRNA processing event that contributes to gene expression by affecting stability, export and translation of mRNA. Human polyadenylation signals (PAS) have core and auxiliary elements that bind polyadenylation factors upstream and downstream of the cleavage site. The majority of mRNAs do not have optimal upstream and downstream core elements and therefore auxiliary elements can aid in polyadenylation efficiency. Auxiliary elements have previously been identified and studied in a small number of mRNAs. We previously used a global approach to examine auxiliary elements to identify overrepresented motifs by a bioinformatic survey. This predicted information was used to direct our in vivo validation studies, all of which were accomplished using both a tandem in vivo polyadenylation assay and using reporter protein assays measured as luciferase activity. Novel auxiliary elements were placed in a test polyadenylation signal. An in vivo polyadenylation assay was used to determine the strength of the polyadenylation signal. All but one of the novel auxiliary elements enhanced the test polyadenylation signal. Effects of these novel auxiliary elements were also measured by a luciferase assay when placed in the 3' UTR of a firefly luciferase reporter. Two novel downstream auxiliary elements and all of the novel upstream auxiliary elements showed an increase in reporter protein levels. Many well known auxiliary polyadenylation elements have been found to occur in multiple sets. However, in our study, multiple copies of novel auxiliary elements brought reporter protein levels as well as polyadenylation choice back to wild type levels. Structural features of these novel auxiliary elements may also affect the role of auxiliary elements. A MS2 structure placed upstream of the polyadenylation signal can affect polyadenylation in both the positive and negative direction. A large change in RNA structure by using novel complementary auxiliary element also decreased polyadenylation choice and reporter protein levels. Therefore, we conclude that RNA structure has an important role in polyadenylation efficiency.

Indexed as

3' Untranslated RegionsPolyadenylationResponse ElementsRNA Processing, Post-TranscriptionalBase SequenceGenes, ReporterHEK293 CellsHeLa CellsHumansLuciferasesMolecular Sequence DatamRNA Cleavage and Polyadenylation FactorsNucleic Acid Conformation3' Untranslated RegionsLuciferasesmRNA Cleavage and Polyadenylation Factors3′ end formationauxiliary elementspolyadenylationregulationRNA structure

Identifiers

PMID23085579
PMCPMC3583856
OpenAlexW1991587024

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.