Evidence map›Paper›PMID 29895222›Full record

ReviewRNA biology2018

Novel roles for Sm-class RNAs in the regulation of gene expression.

Demián Cazalla

Open access · bronzeAbstract readReview
In one paragraph

Review in RNA biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. 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

1 author at 1 institution in 1 country.

Demián Cazallaa Department of Biochemistry , University of Utah School of Medicine , Salt Lake City , UT , USA.ORCID 0000-0002-9076-3655
University of Utah · US

Funding

Novel Functions for Sm-class RNAs in the regulation of gene expressionR01GM118829 · NIGMS · UNIVERSITY OF UTAH · PI CAZALLA, DEMIAN · 2016 to 2020
$1.6M
NIGMS NIH HHS R01 GM118829NIH HHS RO1-GM118829
6 · The paper itself

Abstract

Viruses masterfully regulate host gene expression during infection. Many do so, in part, by expressing non-coding RNAs. Recent work has shown that HSUR 2, a viral non-coding RNA expressed by the oncogenic Herpesvirus saimiri, regulates mRNA expression through a novel mechanism. HSUR 2 base pairs with both target mRNAs and host miRNAs in infected cells. This results in HSUR 2-dependent recruitment of host miRNAs and associated Ago proteins to target mRNAs, and the subsequent destabilization of target mRNAs. Using this mechanism, this virus regulates key cellular pathways during viral infection. Here I discuss the evolution of our thinking about HSUR function and explore the implications of recent findings in relation to the current views on the functions of interactions between miRNAs and other classes of non-coding RNAs, the potential advantages of this mechanism of regulation of gene expression, and the evolutionary origin of HSUR 2.

Indexed as

Gene Expression Regulation, ViralArgonaute ProteinsBase SequenceHerpesviridae InfectionsHerpesvirus 2, SaimiriineHost-Pathogen InteractionsHumansRNA, MessengerRNA, UntranslatedRNA, ViralArgonaute ProteinsRNA, MessengerRNA, UntranslatedRNA, ViralherpesvirusHerpesvirus saimiriHSUR 2miRNA adaptormRNA regulationSm-class RNAViral non-coding RNA

Identifiers

PMID29895222
PMCPMC6161683
OpenAlexW2807729624

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.