Evidence map›Paper›PMID 30926618›Full record

ArticleLife science alliance2019

Sequence and expression levels of circular RNAs in progenitor cell types during mouse corticogenesis.

Martina Dori, Leila Haj Abdullah Alieh, Daniel Cavalli, Simone Massalini, Mathias Lesche, Andreas Dahl, Federico Calegari

Abstract read
In one paragraph

Article in Life science alliance, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
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  4. Review
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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

7 authors.

Martina DoriCRTD-Center for Regenerative Therapies Dresden, School of Medicine, Technische Universität Dresden, Dresden, Germany.ORCID 0000-0002-1053-2006
Leila Haj Abdullah AliehCRTD-Center for Regenerative Therapies Dresden, School of Medicine, Technische Universität Dresden, Dresden, Germany.
Daniel CavalliCRTD-Center for Regenerative Therapies Dresden, School of Medicine, Technische Universität Dresden, Dresden, Germany.ORCID 0000-0002-9861-2181
Simone MassaliniCRTD-Center for Regenerative Therapies Dresden, School of Medicine, Technische Universität Dresden, Dresden, Germany.
Mathias LescheDRESDEN-concept Genome Center c/o Center for Molecular and Cellular Bioengineering, Technische Universität Dresden, Dresden, Germany.ORCID 0000-0002-3274-7163
Andreas DahlDRESDEN-concept Genome Center c/o Center for Molecular and Cellular Bioengineering, Technische Universität Dresden, Dresden, Germany.ORCID 0000-0002-2668-8371
Federico CalegariCRTD-Center for Regenerative Therapies Dresden, School of Medicine, Technische Universität Dresden, Dresden, Germany federico.calegari@tu-dresden.de.ORCID 0000-0002-3703-2802

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circular (circ) RNAs have recently emerged as a novel class of transcripts whose identification and function remain elusive. Among many tissues and species, the mammalian brain is the organ in which circRNAs are more abundant and first evidence of their functional significance started to emerge. Yet, even within this well-studied organ, annotation of circRNAs remains fragmentary, their sequence is unknown, and their expression in specific cell types was never investigated. Overcoming these limitations, here we provide the first comprehensive identification of circRNAs and assessment of their expression patterns in proliferating neural stem cells, neurogenic progenitors, and newborn neurons of the developing mouse cortex. Extending the current knowledge about the diversity of this class of transcripts by the identification of nearly 4,000 new circRNAs, our study is the first to provide the full sequence information and expression patterns of circRNAs in cell types representing the lineage of neurogenic commitment. We further exploited our data by evaluating the coding potential, evolutionary conservation, and biogenesis of circRNAs that we found to arise from a specific subclass of linear mRNAs. Our study provides the arising field of circRNA biology with a powerful new resource to address the complexity and potential biological significance of this new class of transcripts.

Indexed as

Alternative SplicingAnimalsBase SequenceBinding SitesCerebellar CortexExonsFemaleMiceMice, TransgenicMicroRNAsNeurogenesisPregnancyProtein BiosynthesisRNA, CircularRNA, MessengerStem CellsMicroRNAsRNA, CircularRNA, Messenger

Identifiers

PMID30926618
PMCPMC6441494

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Registered trials

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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.