Evidence map›Paper›PMID 31497073›Full record

ArticleMobile DNA2019

Transcriptome analyses of tumor-adjacent somatic tissues reveal genes co-expressed with transposable elements.

Nicky Chung, G M Jonaid, Sophia Quinton, Austin Ross, Corinne E Sexton, Adrian Alberto, Cody Clymer, Daphnie Churchill, Omar Navarro Leija, Mira V Han

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Mobile DNA, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 42 citations in OpenAlex.

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  17. Transposon expression in theGenome research · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Nicky Chung *1School of Life Sciences, University of Nevada, Las Vegas, NV 89154 USA.
G M Jonaid *1School of Life Sciences, University of Nevada, Las Vegas, NV 89154 USA.
Sophia Quinton *1School of Life Sciences, University of Nevada, Las Vegas, NV 89154 USA.
Austin Ross *1School of Life Sciences, University of Nevada, Las Vegas, NV 89154 USA.
Corinne E Sexton1School of Life Sciences, University of Nevada, Las Vegas, NV 89154 USA.
Adrian Alberto2Department of Computer Science, University of Nevada, Las Vegas, NV 89154 USA.
Cody Clymer2Department of Computer Science, University of Nevada, Las Vegas, NV 89154 USA.
Daphnie Churchill2Department of Computer Science, University of Nevada, Las Vegas, NV 89154 USA.
Omar Navarro Leija2Department of Computer Science, University of Nevada, Las Vegas, NV 89154 USA.
Mira V Han1School of Life Sciences, University of Nevada, Las Vegas, NV 89154 USA.ORCID 0000-0002-0488-1170
University of Nevada, Las Vegas · US

Funding

The Genome Analysis and Sequencing Pipeline (GASP)P20GM121325 · NIGMS · UNIVERSITY OF NEVADA LAS VEGAS · PI CHEN, JINGCHUN · 2018 to 2022
$11.5M
Transposable element silencing in human somatic cellsR15GM116108 · NIGMS · UNIVERSITY OF NEVADA LAS VEGAS · PI HAN, MIRA · 2015 to 2015
$353k
NIGMS NIH HHS P20 GM121325NIGMS NIH HHS R15 GM116108
6 · The paper itself

Abstract

backgroundDespite the long-held assumption that transposons are normally only expressed in the germ-line, recent evidence shows that transcripts of transposable element (TE) sequences are frequently found in the somatic cells. However, the extent of variation in TE transcript levels across different tissues and different individuals are unknown, and the co-expression between TEs and host gene mRNAs have not been examined.

resultsHere we report the variation in TE derived transcript levels across tissues and between individuals observed in the non-tumorous tissues collected for The Cancer Genome Atlas. We found core TE co-expression modules consisting mainly of transposons, showing correlated expression across broad classes of TEs. Despite this co-expression within tissues, there are individual TE loci that exhibit tissue-specific expression patterns, when compared across tissues. The core TE modules were negatively correlated with other gene modules that consisted of immune response genes in interferon signaling. KRAB Zinc Finger Proteins (KZFPs) were over-represented gene members of the TE modules, showing positive correlation across multiple tissues. But we did not find overlap between TE-KZFP pairs that are co-expressed and TE-KZFP pairs that are bound in published ChIP-seq studies.

conclusionsWe find unexpected variation in TE derived transcripts, within and across non-tumorous tissues. We describe a broad view of the RNA state for non-tumorous tissues exhibiting higher level of TE transcripts. Tissues with higher level of TE transcripts have a broad range of TEs co-expressed, with high expression of a large number of KZFPs, and lower RNA levels of immune genes.

Indexed as

Co-expressionKRAB zinc fingerL1HSMitochondriaRNA-seqTETransposon

Identifiers

PMID31497073
PMCPMC6720085
OpenAlexW2972280986

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.