Evidence map›Paper›PMID 34782740›Full record

ArticleNature biotechnology2022

Locus-specific expression of transposable elements in single cells with CELLO-seq.

Rebecca V Berrens, Andrian Yang, Christopher E Laumer, Aaron T L Lun, Florian Bieberich, Cheuk-Ting Law, Guocheng Lan, Maria Imaz, Joseph S Bowness, Neil Brockdorff and 2 more

Open access · greenAbstract read
In one paragraph

Article in Nature biotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
13.5field-weighted citation impact, top 1% 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

46 citing papers in PubMed, 83 citations in OpenAlex.

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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

12 authors at 4 institutions in 4 countries.

Rebecca V BerrensCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK. rebecca.berrens@gmail.com.ORCID http://orcid.org/0000-0003-1224-8030
Andrian Yang *European Molecular Biology Laboratory, European Bioinformatics Institute, Cambridge, UK.
Christopher E Laumer *European Molecular Biology Laboratory, European Bioinformatics Institute, Cambridge, UK.
Aaron T L LunCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-3564-4813
Florian BieberichCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
Cheuk-Ting LawCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
Guocheng LanCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0001-9063-5728
Maria ImazWellcome Sanger Institute, Cambridge, UK.ORCID http://orcid.org/0000-0003-1894-8126
Joseph S BownessDevelopmental Epigenetics, Department of Biochemistry, University of Oxford, Oxford, UK.
Neil BrockdorffDevelopmental Epigenetics, Department of Biochemistry, University of Oxford, Oxford, UK.
Daniel J GaffneyWellcome Sanger Institute, Cambridge, UK.ORCID http://orcid.org/0000-0002-1529-1862
John C MarioniCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK. marioni@ebi.ac.uk.
University of Cambridge · GBEuropean Bioinformatics Institute · GBUniversity of Oxford · GBWellcome Sanger Institute · GB

Funding

Cancer Research UK 22231Cancer Research UK A22231Cancer Research UK C9545/A29580Wellcome Trust 213612
6 · The paper itself

Abstract

Transposable elements (TEs) regulate diverse biological processes, from early development to cancer. Expression of young TEs is difficult to measure with next-generation, single-cell sequencing technologies because their highly repetitive nature means that short complementary DNA reads cannot be unambiguously mapped to a specific locus. Single CELl LOng-read RNA-sequencing (CELLO-seq) combines long-read single cell RNA-sequencing with computational analyses to measure TE expression at unique loci. We used CELLO-seq to assess the widespread expression of TEs in two-cell mouse blastomeres as well as in human induced pluripotent stem cells. Across both species, old and young TEs showed evidence of locus-specific expression with simulations demonstrating that only a small number of very young elements in the mouse could not be mapped back to the reference with high confidence. Exploring the relationship between the expression of individual elements and putative regulators revealed large heterogeneity, with TEs within a class showing different patterns of correlation and suggesting distinct regulatory mechanisms.

Indexed as

DNA Transposable ElementsInduced Pluripotent Stem CellsAnimalsHumansMiceRNADNA Transposable ElementsRNA

Identifiers

PMID34782740
PMCPMC7614850
OpenAlexW3213438581

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.