Evidence map›Paper›PMID 24347171›Full record

ArticleThe Journal of biological chemistry2014

The death-inducer obliterator 1 (Dido1) gene regulates embryonic stem cell self-renewal.

Yinyin Liu, Hyeung Kim, Jiancong Liang, Weisi Lu, Bin Ouyang, Dan Liu, Zhou Songyang

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. 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
0.4field-weighted citation impact, top 34% 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, 55 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Bone Morphogenic Protein Signaling and Melanoma.Current treatment options in oncology · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. Exome sequencing in 51 early onset non-familial CRC cases.Molecular genetics & genomic medicine · 2019
    Article
  14. 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 3 institutions in 2 countries.

Yinyin LiuFrom the Key Laboratory of Gene Engineering of the Ministry of Education, Sun Yat-Sen University-Baylor College of Medicine Joint Research Center for Biomedical Sciences, School of Life Sciences and Key Laboratory of Reproductive Medicine of Guangdong Province, the First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China 510275, and.
Hyeung Kim
Jiancong Liang
Weisi Lu
Bin Ouyang
Dan Liu
Zhou Songyang
Baylor College of Medicine · USThe First Affiliated Hospital, Sun Yat-sen University · CNSun Yat-sen University · CN

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
UNDERSTANDING FXTAS AMONG MALES WITH THE FMR1 PREMUTATIONP30HD024064 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI TOLIAS, KIMBERLY R · 1988 to 2013
$29.4M
The Role of p53 in Human Embryonic Stem CellsP01GM081627 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI SONGYANG, ZHOU · 2007 to 2011
$9.9M
Mechanism and Consequences of Telomere DysfunctionR01CA133249 · NCI · BAYLOR COLLEGE OF MEDICINE · PI SONGYANG, ZHOU · 2008 to 2012
$1.6M
Defining the human telomere signaling networks and their implication in cancerR01GM095599 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI SONGYANG, ZHOU · 2011 to 2014
$1.2M
NCI NIH HHS CA133249NCI NIH HHS P30 CA125123NCI NIH HHS P30CA125123NCI NIH HHS R01 CA133249NICHD NIH HHS P30 HD024064NICHD NIH HHS P30HD024064NIGMS NIH HHS GM081627NIGMS NIH HHS GM095599NIGMS NIH HHS P01 GM081627NIGMS NIH HHS R01 GM095599
6 · The paper itself

Abstract

The regulatory network of factors that center on master transcription factors such as Oct4, Nanog, and Sox2 help maintain embryonic stem (ES) cells and ensure their pluripotency. The target genes of these master transcription factors define the ES cell transcriptional landscape. In this study, we report our findings that Dido1, a target of canonical transcription factors such as Oct4, Sox2, and Nanog, plays an important role in regulating ES cell maintenance. We found that depletion of Dido1 in mouse ES cells led to differentiation, and ectopic expression of Dido1 inhibited differentiation induced by leukemia inhibitory factor withdrawal. We further demonstrated that whereas Nanog and Oct4 could occupy the Dido1 locus and promote its transcription, Dido1 could also target to the loci of pluripotency factors such as Nanog and Oct4 and positively regulate their expression. Through this feedback and feedforward loop, Dido1 is able to regulate self-renewal of mouse ES cells.

Indexed as

AnimalsCell DifferentiationCell LineCell ProliferationDNA-Binding ProteinsEmbryonic Stem CellsFeedback, PhysiologicalGene Expression RegulationHomeodomain ProteinsHumansLeukemia Inhibitory FactorMiceNanog Homeobox ProteinOctamer Transcription Factor-3Pluripotent Stem CellsPromoter Regions, GeneticDido protein, mouseDNA-Binding ProteinsHomeodomain ProteinsLeukemia Inhibitory FactorNanog Homeobox ProteinNanog protein, mouseOctamer Transcription Factor-3Pou5f1 protein, mouseTranscription FactorsEmbryonic Stem CellPluripotencySelf-renewalSignal TransductionStem CellsTranscription FactorsTranscription Regulation

Identifiers

PMID24347171
PMCPMC3931039
OpenAlexW2087323952

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.