Evidence map›Paper›PMID 30814272›Full record

ArticleLife science alliance2019

Assessment and site-specific manipulation of DNA (hydroxy-)methylation during mouse corticogenesis.

Florian Noack, Abhijeet Pataskar, Martin Schneider, Frank Buchholz, Vijay K Tiwari, Federico Calegari

Open access · goldAbstract 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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

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  13. The Epigenome in Neurodevelopmental Disorders.Frontiers in neuroscience · 2021
    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

6 authors at 3 institutions in 1 country.

Florian NoackCRTD-Center for Regenerative Therapies, School of Medicine, Technische Universität Dresden, Dresden, Germany.ORCID 0000-0002-2973-0301
Abhijeet PataskarInstitute of Molecular Biology, Mainz, Germany.
Martin SchneiderMedical Systems Biology, School of Medicine, Technische Universität Dresden and Max Planck Institute for Molecular Cell Biology and Genetics, Dresden, Germany.
Frank BuchholzMedical Systems Biology, School of Medicine, Technische Universität Dresden and Max Planck Institute for Molecular Cell Biology and Genetics, Dresden, Germany.
Vijay K TiwariInstitute of Molecular Biology, Mainz, Germany.
Federico CalegariCRTD-Center for Regenerative Therapies, School of Medicine, Technische Universität Dresden, Dresden, Germany federico.calegari@tu-dresden.de.ORCID 0000-0002-3703-2802
Center for Systems Biology Dresden · DEInstitute of Molecular Biology · DETechnische Universität Dresden · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dynamic changes in DNA (hydroxy-)methylation are fundamental for stem cell differentiation. However, the signature of these epigenetic marks in specific cell types during corticogenesis is unknown. Moreover, site-specific manipulation of cytosine modifications is needed to reveal the significance and function of these changes. Here, we report the first assessment of (hydroxy-)methylation in neural stem cells, neurogenic progenitors, and newborn neurons during mammalian corticogenesis. We found that gain in hydroxymethylation and loss in methylation occur sequentially at specific cellular transitions during neurogenic commitment. We also found that these changes predominantly occur within enhancers of neurogenic genes up-regulated during neurogenesis and target of pioneer transcription factors. We further optimized the use of dCas9-Tet1 manipulation of (hydroxy-)methylation, locus-specifically, in vivo, showing the biological relevance of our observations for

Indexed as

5-MethylcytosineAnimalsCadherinsCell DifferentiationCell LineageCRISPR-Associated Protein 9CytosineDNA-Binding ProteinsDNA MethylationEmbryonic Stem CellsEpigenesis, GeneticFemaleGene Expression Regulation, DevelopmentalMiceMice, Inbred C57BLNeural Stem Cells5-hydroxymethylcytosine5-MethylcytosineCadherinsCRISPR-Associated Protein 9CytosineDchs1 protein, mouseDNA-Binding ProteinsOncogene Proteins, FusionProto-Oncogene ProteinsTET1 protein, mouseTranscription Factors

Identifiers

PMID30814272
PMCPMC6394126
OpenAlexW2915391406

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.