Evidence map›Paper›PMID 31304631›Full record

ArticleThe EMBO journal2019

DSCR1-mediated TET1 splicing regulates miR-124 expression to control adult hippocampal neurogenesis.

Chiyeol Choi, Taehoon Kim, Karen T Chang, Kyung-Tai Min

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 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 21% 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, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Epigenetic regulation in adult neural stem cells.Frontiers in cell and developmental biology · 2024
    Review
  5. Review
  6. Article
  7. Review
  8. New Insights into TETs in Psychiatric Disorders.International journal of molecular sciences · 2022
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
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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

4 authors at 2 institutions in 2 countries.

Chiyeol ChoiDepartment of Biological Sciences, School of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Korea.
Taehoon KimDepartment of Biological Sciences, School of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Korea.
Karen T ChangZilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Kyung-Tai MinDepartment of Biological Sciences, School of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Korea.ORCID 0000-0003-0983-4258
Ulsan National Institute of Science and Technology · KRUniversity of Southern California · US

Funding

Role of DYRK1A/MNB in Synaptic growth and functionR01NS080946 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KAREN T CHANG · 2013 to 2026
$5.0M
Molecular mechanisms underlying activity-induced synaptic remodelingR01NS102260 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHANG, KAREN T · 2018 to 2022
$2.2M
NIH HHS NS080946NIH HHS NS102260NINDS NIH HHS R01 NS080946NINDS NIH HHS R01 NS102260
6 · The paper itself

Abstract

Whether epigenetic factors such as DNA methylation and microRNAs interact to control adult hippocampal neurogenesis is not fully understood. Here, we show that Down syndrome critical region 1 (DSCR1) protein plays a key role in adult hippocampal neurogenesis by modulating two epigenetic factors: TET1 and miR-124. We find that DSCR1 mutant mice have impaired adult hippocampal neurogenesis. DSCR1 binds to TET1 introns to regulate splicing of TET1, thereby modulating TET1 level. Furthermore, TET1 controls the demethylation of the miRNA-124 promoter to modulate miR-124 expression. Correcting the level of TET1 in DSCR1 knockout mice is sufficient to prevent defective adult neurogenesis. Importantly, restoring DSCR1 level in a Down syndrome mouse model effectively rescued adult neurogenesis and learning and memory deficits. Our study reveals that DSCR1 plays a critical upstream role in epigenetic regulation of adult neurogenesis and provides insights into potential therapeutic strategy for treating cognitive defects in Down syndrome.

Indexed as

RNA SplicingAnimalsCells, CulturedDisease Models, AnimalDNA-Binding ProteinsDown SyndromeEpigenesis, GeneticGene Knockdown TechniquesHippocampusHumansMaleMiceMice, TransgenicMicroRNAsMixed Function OxygenasesMuscle ProteinsDNA-Binding ProteinsMicroRNAsMIRN124 microRNA, humanMixed Function OxygenasesMuscle ProteinsProto-Oncogene ProteinsRCAN1 protein, humanTET1 protein, humanadult hippocampal neurogenesisDown syndromeDSCR1miR-124TET1

Identifiers

PMID31304631
PMCPMC6627232
OpenAlexW2949266876

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.