Evidence map›Paper›PMID 26863630›Full record

ArticleOncotarget2016

EIF2S3Y suppresses the pluripotency state and promotes the proliferation of mouse embryonic stem cells.

Na Li, Hailong Mu, Liming Zheng, Bo Li, Chongyang Wu, Bowen Niu, Qiaoyan Shen, Xin He, Jinlian Hua

Abstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Microcephaly GeneInternational journal of molecular sciences · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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

9 authors.

Na LiCollege of Veterinary Medicine, Shaanxi Center of Stem Cells Engineering and Technology, Northwest A & F University, Yangling, Shaanxi, China.
Hailong MuCollege of Veterinary Medicine, Shaanxi Center of Stem Cells Engineering and Technology, Northwest A & F University, Yangling, Shaanxi, China.
Liming ZhengCollege of Veterinary Medicine, Shaanxi Center of Stem Cells Engineering and Technology, Northwest A & F University, Yangling, Shaanxi, China.
Bo LiCollege of Veterinary Medicine, Shaanxi Center of Stem Cells Engineering and Technology, Northwest A & F University, Yangling, Shaanxi, China.
Chongyang WuCollege of Veterinary Medicine, Shaanxi Center of Stem Cells Engineering and Technology, Northwest A & F University, Yangling, Shaanxi, China.
Bowen NiuCollege of Veterinary Medicine, Shaanxi Center of Stem Cells Engineering and Technology, Northwest A & F University, Yangling, Shaanxi, China.
Qiaoyan ShenCollege of Veterinary Medicine, Shaanxi Center of Stem Cells Engineering and Technology, Northwest A & F University, Yangling, Shaanxi, China.
Xin HeCollege of Veterinary Medicine, Shaanxi Center of Stem Cells Engineering and Technology, Northwest A & F University, Yangling, Shaanxi, China.
Jinlian HuaCollege of Veterinary Medicine, Shaanxi Center of Stem Cells Engineering and Technology, Northwest A & F University, Yangling, Shaanxi, China.

Funding

NIAAA NIH HHS L30 AA021605
6 · The paper itself

Abstract

Eukaryotic translation initiation factor 2, subunit 3, and structural gene Y-linked (EIF2S3Y) is essential for spermatogenesis in mouse models. However, its effect on embryonic stem (ES) cells remains unknown. In our observation, differentiated ES cells showed higher levels of EIF2S3Y. To further elucidate its role in ES cells, we utilized ES-derived EIF2S3Y-overexpressing cells and found that EIF2S3Y down-regulated the pluripotency state of ES cells, which might be explained by decreased histone methylation levels because of reduced levels of ten-eleven translocation 1 (TET1). Moreover, EIF2S3Y-overexpressing cells showed an enhanced proliferation rate, which might be due to increased Cyclin A and Cyclin E levels. This study highlighted novel roles of EIF2S3Y in the pluripotency maintenance and proliferation control of ES cells, which would provide an efficient model to study germ cell generation as well as cancer development using ES cells, thus providing valuable target for clinical applications of ES cells.

Indexed as

AnimalsCell DifferentiationCell LineCell ProliferationCyclin ACyclin EDNA-Binding ProteinsHistonesMaleMethylationMiceMice, Inbred ICRMouse Embryonic Stem CellsPluripotent Stem CellsProto-Oncogene ProteinsTranscription FactorsCyclin ACyclin EDNA-Binding ProteinsEif2s3y protein, mouseHistonesProto-Oncogene ProteinsTET1 protein, mouseTranscription FactorsEIF2S3Yembryonic stem cellsmousepluripotencyproliferation

Identifiers

PMID26863630
PMCPMC4905476

What OpenQuestion holds

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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.