Evidence map›Paper›PMID 32332169›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Induction of recurrent break cluster genes in neural progenitor cells differentiated from embryonic stem cells in culture.

Aseda Tena, Yuxiang Zhang, Nia Kyritsis, Anne Devorak, Jeffrey Zurita, Pei-Chi Wei, Frederick W Alt

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  4. Review
  5. Article
  6. Article
  7. Replication stress causes delayed mitotic entry and chromosome 12 fragility at the ANKS1B large neuronal gene in human induced pluripotent stem cells.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2023
    Article
  8. Article
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  12. WWOX Loss of Function in Neurodevelopmental and Neurodegenerative Disorders.International journal of molecular sciences · 2020
    Review
  13. 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

7 authors at 2 institutions in 1 country.

Aseda TenaProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
Yuxiang ZhangProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
Nia KyritsisProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
Anne DevorakProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
Jeffrey ZuritaProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
Pei-Chi WeiProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115; p.wei@dkfz-heidelberg.de alt@enders.tch.harvard.edu.
Frederick W AltProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115; p.wei@dkfz-heidelberg.de alt@enders.tch.harvard.edu.
Harvard University · USBoston Children's Hospital · US

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

Mild replication stress enhances appearance of dozens of robust recurrent genomic break clusters, termed RDCs, in cultured primary mouse neural stem and progenitor cells (NSPCs). Robust RDCs occur within genes ("RDC-genes") that are long and have roles in neural cell communications and/or have been implicated in neuropsychiatric diseases or cancer. We sought to develop an in vitro approach to determine whether specific RDC formation is associated with neural development. For this purpose, we adapted a system to induce neural progenitor cell (NPC) development from mouse embryonic stem cell (ESC) lines deficient for XRCC4 plus p53, a genotype that enhances DNA double-strand break (DSB) persistence to enhance detection. We tested for RDCs by our genome-wide DSB identification approach that captures DSBs via their ability to join to specific genomic Cas9/single-guide RNA-generated bait DSBs. In XRCC4/p53-deficient ESCs, we detected seven RDCs, all of which were in genes and two of which were robust. In contrast, in NPCs derived from these ESC lines we detected 29 RDCs, a large fraction of which were robust and associated with long, transcribed neural genes that were also robust RDC-genes in primary NSPCs. These studies suggest that many RDCs present in NSPCs are developmentally influenced to occur in this cell type and indicate that induced development of NPCs from ESCs provides an approach to rapidly elucidate mechanistic aspects of NPC RDC formation.

Indexed as

AnimalsCell DifferentiationCell LineCells, CulturedDNA-Binding ProteinsDNA BreaksDNA ReplicationEmbryonic Stem CellsGenes, p53GenomeHumansMiceMouse Embryonic Stem CellsMultigene FamilyNeural Stem CellsNeurogenesisDNA-Binding ProteinsXRCC4 protein, humanXRCC4 protein, mousedifferentiated neural progenitor cellsembryonic stem cellsrecurrent DNA break cluster genestranscription

Identifiers

PMID32332169
PMCPMC7229678
OpenAlexW3019662164

What OpenQuestion holds

Textmetadata
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.