Evidence map›Paper›PMID 29099484›Full record

ArticleCell death and differentiation2018

Lin28B and miR-142-3p regulate neuronal differentiation by modulating Staufen1 expression.

Younseo Oh, Jungyun Park, Jin-Il Kim, Mi-Yoon Chang, Sang-Hun Lee, Youl-Hee Cho, Jungwook Hwang

Open access · bronzeAbstract read
In one paragraph

Article in Cell death and differentiation, 2018. 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, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Interaction between miR-142-3p andInternational journal of molecular sciences · 2024
    Article
  7. Article
  8. Article
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  10. YTHDF2 destabilizes mRNA (New York, N.Y.) · 2020
    Article
  11. Small changes, big implications: The impact of mBiochimica et biophysica acta. Gene regulatory mechanisms · 2019
    Review
  12. Article
  13. Article
  14. miR-483-3p promotes proliferation and migration of neuroblastoma cells by targeting PUMA.International journal of clinical and experimental pathology · 2018
    Article
  15. 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

7 authors at 2 institutions in 1 country.

Younseo OhGraduate School for Biomedical Science & Engineering, Seoul, Korea.
Jungyun ParkGraduate School for Biomedical Science & Engineering, Seoul, Korea.
Jin-Il KimGraduate School for Biomedical Science & Engineering, Seoul, Korea.
Mi-Yoon ChangHanyang Biomedical Research Institute, Seoul, Korea.
Sang-Hun LeeDepartment of Biochemistry and Molecular Biology, College of Medicine, Seoul, Korea.
Youl-Hee ChoDepartment of Medical Genetics, College of Medicine, Hanyang University, Seoul, Korea.
Jungwook HwangGraduate School for Biomedical Science & Engineering, Seoul, Korea.ORCID 0000-0002-2290-1649
Bio-Medical Science (South Korea) · KRHanyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Staufen1 (STAU1) and Lin28B are RNA-binding proteins that are involved in neuronal differentiation as a function of post-transcriptional regulation. STAU1 triggers post-transcriptional regulation, including mRNA export, mRNA relocation, translation and mRNA decay. Lin28B also has multiple functions in miRNA biogenesis and the regulation of translation. Here, we examined the connection between STAU1 and Lin28B and found that Lin28B regulates the abundance of STAU1 mRNA via miRNA maturation. Decreases in the expression of both STAU1 and Lin28B were observed during neuronal differentiation. Depletion of STAU1 or Lin28B inhibited neuronal differentiation, and overexpression of STAU1 or Lin28B enhanced neuronal differentiation. Interestingly, the stability of STAU1 mRNA was modulated by miR-142-3p, whose maturation was regulated by Lin28B. Thus, miR-142-3p expression increased as Lin28B expression decreased during differentiation, leading to the reduction of STAU1 expression. The transcriptome from Staufen-mediated mRNA decay (SMD) targets during differentiation was analyzed, confirming that STAU1 was a key factor in neuronal differentiation. In support of this finding, regulation of STAU1 expression in mouse neural precursor cells had the same effects on neuronal differentiation as it did in human neuroblastoma cells. These results revealed the collaboration of two RNA-binding proteins, STAU1 and Lin28B, as a regulatory mechanism in neuronal differentiation.

Indexed as

Cell DifferentiationAnimalsCytoskeletal ProteinsHeLa CellsHumansMiceMicroRNAsNeural Stem CellsRNA-Binding ProteinsTumor Cells, CulturedCytoskeletal ProteinsLIN28B protein, humanMicroRNAsMIRN142 microRNA, humanRNA-Binding ProteinsSTAU1 protein, human

Identifiers

PMID29099484
PMCPMC5762855
OpenAlexW2766901760

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.