Evidence map›Paper›PMID 29907706›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2018

Widespread Effects of Chemokine 3' Untranslated Regions on mRNA Degradation and Protein Production in Human Cells.

Wenxue Zhao, David J Erle

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

1 citing paper in PubMed, 9 citations in OpenAlex.

  1. Review
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 2 countries.

Wenxue ZhaoLung Biology Center, Department of Medicine, University of California, San Francisco, San Francisco, CA 94158; and wzhao_sysu@163.com david.erle@ucsf.edu.
David J ErleLung Biology Center, Department of Medicine, University of California, San Francisco, San Francisco, CA 94158; and wzhao_sysu@163.com david.erle@ucsf.edu.ORCID 0000-0002-2171-0648
Sun Yat-sen University · CNUniversity of California, San Francisco · US

Funding

Massively parallel identification of functional 3' UTR variants in asthmaR01HL124285 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ERLE, DAVID J · 2014 to 2017
$2.2M
Empiric deconvolution of functional RNA elementsR01GM110251 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ERLE, DAVID J, MCMANUS, MICHAEL T · 2014 to 2017
$2.2M
Tools for high-throughput functional analysis of 3' UTR cis-regulatory elementsR21HG004665 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ERLE, DAVID J · 2008 to 2009
$386k
NHGRI NIH HHS R21 HG004665NHLBI NIH HHS R01 HL124285NIGMS NIH HHS R01 GM110251
6 · The paper itself

Abstract

Chemokines are a large family of chemotactic cytokines that play critical roles in inflammation, development, and diseases. Chemokine expression is highly regulated during development and in response to environmental stimuli. The 3' untranslated regions (3'-UTRs) of mRNA are believed to be important in the control of chemokine gene expression. However, the regulatory effects of most chemokine 3'-UTRs have not been characterized previously. In this work, we systematically studied the effects of 43 CC and CXC chemokine 3'-UTRs on gene expression in eight human cell lines and two types of human primary cells. We found that chemokine 3'-UTRs had a wide spectrum of regulatory effects on mRNA abundance and protein production that were tightly correlated with the effects on mRNA stability. In general, 3'-UTRs had remarkably similar effects across all cell types studied. The presence of AU-rich elements, microRNA targets, and Pumilio binding sites were associated with chemokine 3'-UTR activity but did not fully account for all 3'-UTR activity detected using the reporter assay. Mutational analysis illustrated how specific

Indexed as

3' Untranslated RegionsBinding SitesCell Line, TumorChemokinesGene ExpressionGenes, ReporterHumansJurkat CellsProtein BindingRegulatory Sequences, Nucleic AcidRNA, MessengerRNA Stability3' Untranslated RegionsChemokinesRNA, Messenger

Identifiers

PMID29907706
PMCPMC6057839
OpenAlexW2808421308

What Socratic 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 Socratic graph.