Evidence map›Paper›PMID 27411104›Full record

ArticleStem cell reports2016

CDK7 and miR-210 Co-regulate Cell-Cycle Progression of Neural Progenitors in the Developing Neocortex.

Aisha I Abdullah, Haijun Zhang, Yanzhen Nie, Wei Tang, Tao Sun

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. miR-409-3p repressesFrontiers in neuroscience · 2022
    Article
  6. Article
  7. Review
  8. Article
  9. An evolutionarily acquired microRNA shapes development of mammalian cortical projections.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  10. CDK7 inhibitors as anticancer drugs.Cancer metastasis reviews · 2020
    Review
  11. Article
  12. Review
  13. Review
  14. The essential and multifunctional TFIIH complex.Protein science : a publication of the Protein Society · 2018
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
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

5 authors at 3 institutions in 2 countries.

Aisha I AbdullahDepartment of Cell and Developmental Biology, Cornell University Weill Medical College, 1300 York Avenue, Box 60, New York, NY 10065, USA.
Haijun ZhangDepartment of Cell and Developmental Biology, Cornell University Weill Medical College, 1300 York Avenue, Box 60, New York, NY 10065, USA; Department of Genetic Medicine, Cornell University Weill Medical College, 1300 York Avenue, New York, NY 10065, USA.
Yanzhen NieShanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China.
Wei TangShanghai Jiao Tong University School of Medicine, Ruijin Hospital, 197 2nd Ruijin Road, Shanghai 200025, China. Electronic address: tina_tangwei@163.com.
Tao SunDepartment of Cell and Developmental Biology, Cornell University Weill Medical College, 1300 York Avenue, Box 60, New York, NY 10065, USA. Electronic address: tas2009@med.cornell.edu.
Cornell University · USRuijin Hospital · CNShanghai Jiao Tong University · CN

Funding

MicroRNA Function in the Development of the Cerebral CortexR01MH083680 · NIMH · WEILL MEDICAL COLL OF CORNELL UNIV · PI DE MARCO GARCIA, NATALIA VANESA, STUHLMANN, HEIDI · 2009 to 2018
$4.2M
Training Program in Developmental BiologyT32HD060600 · NICHD · WEILL MEDICAL COLL OF CORNELL UNIV · PI BAO, ZHIRONG, STUHLMANN, HEIDI · 2010 to 2024
$3.5M
NICHD NIH HHS T32 HD060600NIMH NIH HHS R01 MH083680
6 · The paper itself

Abstract

The molecular mechanisms regulating neural progenitor (NP) proliferation are fundamental in establishing the cytoarchitecture of the mammalian neocortex. The rate of cell-cycle progression and a fine-tuned balance between cell-cycle re-entry and exit determine the numbers of both NPs and neurons as well as postmitotic neuronal laminar distribution in the cortical wall. Here, we demonstrate that the microRNA (miRNA) miR-210 is required for normal mouse NP cell-cycle progression. Overexpression of miR-210 promotes premature cell-cycle exit and terminal differentiation in NPs, resulting in an increase in early-born postmitotic neurons. Conversely, miR-210 knockdown promotes an increase in the radial glial cell population and delayed differentiation, resulting in an increase in late-born postmitotic neurons. Moreover, the cyclin-dependent kinase CDK7 is regulated by miR-210 and is necessary for normal NP cell-cycle progression. Our findings demonstrate that miRNAs are essential for normal NP proliferation and cell-cycle progress during neocortical development.

Indexed as

AnimalsCell CycleCell DifferentiationCell ProliferationCyclin-Dependent Kinase-Activating KinaseCyclin-Dependent KinasesEmbryo, MammalianGene Expression Regulation, DevelopmentalHumansMiceMicroRNAsNeocortexNeural Stem CellsNeurogenesisNeuronsCyclin-Dependent Kinase-Activating KinaseCyclin-Dependent KinasesMicroRNAsMIRN210 microRNA, mouseCDK7cell cyclemicroRNAmiR-210neocortexneural progenitor

Identifiers

PMID27411104
PMCPMC4944761
OpenAlexW2471188129

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.