Evidence map›Paper›PMID 24049083›Full record

ArticleNucleic acids research2014

A regulatory circuit comprising GATA1/2 switch and microRNA-27a/24 promotes erythropoiesis.

Fang Wang, Yong Zhu, Lihua Guo, Lei Dong, Huiwen Liu, Haixin Yin, Zhongzu Zhang, Yuxia Li, Changzheng Liu, Yanni Ma and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. MicroRNAs in ovarian follicular atresia and granulosa cell apoptosis.Reproductive biology and endocrinology : RB&E · 2019
    Review
  10. Cooperative and Independent Functions of theInternational journal of molecular sciences · 2018
    Article
  11. Haematologica · 2018
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. miRNA143 Induces K562 Cell Apoptosis Through Downregulating BCR-ABL.Medical science monitor : international medical journal of experimental and clinical research · 2016
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 2 countries.

Fang WangDepartment of Biochemistry, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences (CAMS) & Peking Union Medical College (PUMC), Beijing 100005, PR China, Zebrafish Core Facility, State Key Laboratory of Medical Molecular Sciences, Institute of Basic Medical Sciences, CAMS & PUMC, Beijing 100005, PR China, Department of Biomedical Engineering, School of Computation and Information Technology, Beijing Jiaotong University, Beijing 100044, PR China, Department of Cardiology, Children's Hospital Boston, Boston, MA 02115, USA, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China and Cancer Center, The General Hospital of the People's Liberation Army, Beijing 100853, PR China.
Yong Zhu
Lihua Guo
Lei Dong
Huiwen Liu
Haixin Yin
Zhongzu Zhang
Yuxia Li
Changzheng Liu
Yanni Ma
Wei Song
Aibin He
Qiang Wang
Linfang Wang
Junwu Zhang
Jianxiong Li
Jia Yu
Peking Union Medical College Hospital · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNBeijing Jiaotong University · CNBoston Children's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transcriptional networks orchestrate complex developmental processes, and such networks are commonly instigated by master regulators for development. By now, considerable progress has been made in elucidating GATA factor-dependent genetic networks that control red blood cell development. Here we reported that GATA-1 and GATA-2 co-regulated the expression of two microRNA genes, microRNA-27a and microRNA-24, with critical roles in regulating erythroid differentiation. In general, GATA-2 occupied the miR-27a≈24 promoter and repressed their transcription in immature erythroid progenitor cells. As erythropoiesis proceeded, GATA-1 directly activated miR-27a≈24 transcription, and this involved a GATA-1-mediated displacement of GATA-2 from chromatin, a process termed 'GATA switch'. Furthermore, the mature miR-27a and miR-24 cooperatively inhibited GATA-2 translation and favoured the occupancy switch from GATA-2 to GATA-1, thus completing a positive feedback loop to promote erythroid maturation. In line with the essential role of GATA factors, ectopic expression of miR-27a or miR-24 promoted erythropoiesis in human primary CD34+ haematopoietic progenitor cells and mice, whereas attenuated miR-27 or miR-24 level led to impaired erythroid phenotypes in haematopoietic progenitor cells and zebrafish. Taken together, these data integrated micro RNA expression and function into GATA factor coordinated networks and provided mechanistic insight into a regulatory circuit that comprised GATA1/2 switch and miR-27a/24 in erythropoiesis.

Indexed as

AnimalsCells, CulturedErythrocytesErythroid CellsErythropoiesisGATA1 Transcription FactorGATA2 Transcription FactorGene Regulatory NetworksHematopoietic Stem CellsHumansK562 CellsMaleMiceMice, Inbred C57BLMicroRNAsPromoter Regions, GeneticGATA1 Transcription FactorGATA2 Transcription FactorMicroRNAsMIRN23a microRNA, humanMIRN24 microRNA, humanMIRN27 microRNA, human

Identifiers

PMID24049083
PMCPMC3874166
OpenAlexW2023398004

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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.