Evidence map›Paper›PMID 28350000›Full record

ArticleScientific reports2017

Engineering Structurally Interacting RNA (sxRNA).

Francis Doyle, Sameer Lapsia, Salvatore Spadaro, Zachary E Wurz, Sumita Bhaduri-McIntosh, Scott A Tenenbaum

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. RNA Engineering for Public Health: Innovations in RNA-Based Diagnostics and Therapeutics.Annual review of chemical and biomolecular engineering · 2021
    Article
  4. Article
  5. Article
  6. Article
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 4 institutions in 1 country.

Francis DoyleNanobioscience Constellation, College of Nanoscale Science and Engineering, SUNY Polytechnic Institute, Albany, NY New York 12203, USA.
Sameer LapsiaDepartment of Pediatrics, Stony Brook University School of Medicine, Stony Brook, NY 11794, USA.
Salvatore SpadaroDepartment of Pediatrics, Stony Brook University School of Medicine, Stony Brook, NY 11794, USA.
Zachary E WurzHocusLocus, LLC, 253 Fuller Road, Nanofab North, Albany NY 12203, USA.
Sumita Bhaduri-McIntoshPediatric Infectious Diseases, Departments of Pediatrics and Molecular Genetics and Microbiology, Stony Brook University School of Medicine, Stony Brook, NY 11794, USA.
Scott A TenenbaumNanobioscience Constellation, College of Nanoscale Science and Engineering, SUNY Polytechnic Institute, Albany, NY New York 12203, USA.
Stony Brook University · USSUNY Polytechnic Institute · USChildren's Hospital of The King's Daughters · USHocuslocus (United States) · US

Funding

Comprehensive Identification of ENCODE RNA based Cis-Regulatory ElementsU01HG004571 · NHGRI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI TENENBAUM, SCOTT A · 2007 to 2011
$2.6M
Host determinants of Epstein-Barr virus lytic cycle activationR01AI113134 · NIAID · UNIVERSITY OF FLORIDA · PI BHADURI-MCINTOSH, SUMITA · 2014 to 2018
$1.9M
In-vivo miRNA Detection Using Structurally Interacting RNA (sxRNA)R41GM097811 · NIGMS · HOCUSLOCUS, INC. · PI TENENBAUM, SCOTT A · 2011 to 2011
$294k
sxRNA-based Antiviral Approach targeting Epstein-Barr virusR41AI115834 · NIAID · HOCUSLOCUS, INC. · PI BHADURI-MCINTOSH, SUMITA · 2015 to 2015
$225k
A Novel Approach to Purifying iPSC Derived Cell CulturesR41GM114935 · NIGMS · HOCUSLOCUS, INC. · PI TENENBAUM, SCOTT A · 2015 to 2015
$225k
NHGRI NIH HHS U01 HG004571NIAID NIH HHS R01 AI113134NIAID NIH HHS R41 AI115834NIGMS NIH HHS R41 GM097811NIGMS NIH HHS R41 GM114935
6 · The paper itself

Abstract

RNA-based three-way junctions (3WJs) are naturally occurring structures found in many functional RNA molecules including rRNA, tRNA, snRNA and ribozymes. 3WJs are typically characterized as resulting from an RNA molecule folding back on itself in cis but could also form in trans when one RNA, for instance a microRNA binds to a second structured RNA, such as a mRNA. Trans-3WJs can influence the final shape of one or both of the RNA molecules and can thus provide a means for modulating the availability of regulatory motifs including potential protein or microRNA binding sites. Regulatory 3WJs generated in trans represent a newly identified regulatory category that we call structurally interacting RNA or sxRNA for convenience. Here we show that they can be rationally designed using familiar cis-3WJ examples as a guide. We demonstrate that an sxRNA "bait" sequence can be designed to interact with a specific microRNA "trigger" sequence, creating a regulatable RNA-binding protein motif that retains its functional activity. Further, we show that when placed downstream of a coding sequence, sxRNA can be used to switch "ON" translation of that sequence in the presence of the trigger microRNA and the amount of translation corresponded with the amount of microRNA present.

Indexed as

Nucleic Acid ConformationBinding SitesCell Line, TumorHumansMicroRNAsRNA, CatalyticRNA, RibosomalRNA, Small NuclearRNA, TransferMicroRNAsRNA, CatalyticRNA, RibosomalRNA, Small NuclearRNA, Transfer

Identifiers

PMID28350000
PMCPMC5368982
OpenAlexW2601526534

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.