Evidence map›Paper›PMID 23707624›Full record

ArticleMethods (San Diego, Calif.)2013

Organic small hairpin RNAs (OshR): a do-it-yourself platform for transgene-based gene silencing.

Mei Zeng, Marissa S Kuzirian, Lamia Harper, Suzanne Paradis, Takuya Nakayama, Nelson C Lau

Open access · greenAbstract read
In one paragraph

Article in Methods (San Diego, Calif.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 44% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 2 institutions in 1 country.

Mei ZengDepartment of Biology, Brandeis University, United States; Rosenstiel Basic Medical Science Research Center, United States.
Marissa S Kuzirian
Lamia Harper
Suzanne Paradis
Takuya Nakayama
Nelson C Lau
Brandeis University · USUniversity of Virginia · US

Funding

NEUROSCIENCE: FROM CHANNELS TO BEHAVIORT32MH019929 · NIMH · BRANDEIS UNIVERSITY · PI GRIFFITH, LESLIE C · 1994 to 2023
$8.5M
Genetic Control of Early Retinal DevelopmentR01EY017400 · NEI · UNIVERSITY OF VIRGINIA · PI GRAINGER, ROBERT M · 2006 to 2010
$1.8M
Genomic survey of cis-regulatory element function by high-throughput transgenesisR01EY018000 · NEI · UNIVERSITY OF VIRGINIA · PI GRAINGER, ROBERT M · 2009 to 2012
$1.3M
The Function of piRNAs and the piRNA ComplexR00HD057298 · NICHD · BRANDEIS UNIVERSITY · PI LAU, NELSON C · 2009 to 2011
$706k
Identification of the Protein Kinases which Regulate Mammalian Synapse FormationR21DA026977 · NIDA · BRANDEIS UNIVERSITY · PI PARADIS, SUZANNE · 2009 to 2010
$316k
NEI NIH HHS EY017400NEI NIH HHS EY018000NEI NIH HHS R01 EY017400NEI NIH HHS R01 EY018000NICHD NIH HHS R00 HD057298NICHD NIH HHS R00HD057298NIDA NIH HHS R21 DA026977NIDA NIH HHS R21DA026977NIMH NIH HHS T32 MH019929
6 · The paper itself

Abstract

The RNA interference (RNAi) pathway in animal cells can be harnessed to silence gene expression with artificial small interfering RNAs (siRNAs) or transgenes that express small hairpin RNAs (shRNAs). The transgene-expressing shRNA approach has been adapted into large-scale resources for genome-wide loss-of-function screens, whereas focused studies on a narrow set of genes can be achieved by using individual shRNA constructs from these resources. Although current shRNA repositories generally work, they might fail in certain situations and therefore necessitate other alternatives. We detail here a new highly-accessible and rational design of custom shRNAs that utilizes a refined backbone configuration termed the 'organic' shRNA (OshR) platform. The OshR platform is 'organic' because it conforms more naturally to the endogenous vertebrate miRNAs by maintaining specific bulges and incorporating strategic mismatches to insure the desired guide strand is produced while reducing the accumulation of passenger strands that might contribute to off-target effects. We also demonstrate that the reliability of the OshR platform for gene silencing is increased when sequences target the 3' UnTranslated Region (3'UTR) of a gene. We further compare the OshR platform with the current and emerging shRNA designs, and propose that the OshR platform is a novel approach that can allow investigators to generate custom and effective shRNAs for individual gene functional studies.

Indexed as

Transgenes3' Untranslated RegionsAnimalsBase PairingBase SequenceCloning, MolecularGene Knockdown TechniquesHEK293 CellsHumansMiceMicroRNAsMolecular Sequence DataMonophenol MonooxygenaseNIMA-Related KinasesProtein Serine-Threonine KinasesRNA Interference3' Untranslated RegionsMicroRNAsMIRN451 microRNA, humanMonophenol MonooxygenaseNek2 protein, mouseNIMA-Related KinasesProtein Serine-Threonine KinasesRNA, MessengerRNA, Small InterferingXenopus ProteinsGene silencingRNA interferenceshRNA

Identifiers

PMID23707624
PMCPMC3966114
OpenAlexW2025482191

What OpenQuestion holds

Textmetadata
LicenceTDM
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.