Evidence map›Paper›PMID 11897870›Full record

ArticleStem cells (Dayton, Ohio)2002

Analysis of different promoter systems for efficient transgene expression in mouse embryonic stem cell lines.

Sangmi Chung, Therese Andersson, Kai-C Sonntag, Lars Björklund, Ole Isacson, Kwang-Soo Kim

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

57 citing papers in PubMed, 151 citations in OpenAlex.

  1. Article
  2. Human stem cell-specific epigenetic signatures control transgene expression.Biochimica et biophysica acta. Gene regulatory mechanisms · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. A review of the tortuous path of nonviral gene delivery and recent progress.International journal of biological macromolecules · 2021
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. AAV9 Edits Muscle Stem Cells in Normal and Dystrophic Adult Mice.Molecular therapy : the journal of the American Society of Gene Therapy · 2019
    Article
  13. Article
  14. Using a Commonly Down-Regulated Cytomegalovirus (CMV) Promoter for High-Level Expression of Ectopic Gene in a Human B Lymphoma Cell Line.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  15. Article
  16. Differential control of retrovirus silencing in embryonic cells by proteasomal regulation of the ZFP809 retroviral repressor.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  17. F1000Research · 2017
    Review
  18. Article
  19. Review
  20. 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

6 authors at 2 institutions in 1 country.

Sangmi ChungMolecular Neurobiology Laboratory, McLean Hospital, Harvard Medical School, Belmont, Massachusetts 02478, USA.
Therese Andersson
Kai-C Sonntag
Lars Björklund
Ole Isacson
Kwang-Soo Kim
Harvard University · USMcLean Hospital · US

Funding

Transplantation of ES Cell-derived DA Neurons into PD Primate ModelsP50NS039793 · NINDS · MC LEAN HOSPITAL (BELMONT, MA) · PI ISACSON, OLE · 1999 to 2010
$16.3M
Transcriptional regulatory cascade of midbrain dopamine neuron development by PitR01MH048866 · NIMH · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI KIM, KWANG-SOO · 1998 to 2012
$3.7M
Functional Roles of Nurr1 for Midbrain Dopamine Neurons in Health and DiseaseR01NS084869 · NINDS · MCLEAN HOSPITAL · PI KIM, KWANG-SOO · 2014 to 2018
$1.7M
TRANSCRIPTIONAL MECHANISMS OF TH GENE EXPRESSIONR29MH048866 · NIMH · WINIFRED MASTERSON BURKE MED RES INST · PI KIM, KWANG-SOO · 1992 to 1996
–
NIMH NIH HHS MH 48866NIMH NIH HHS R01 MH048866NIMH NIH HHS R29 MH048866NINDS NIH HHS P50 NS039793NINDS NIH HHS P50 NS 39793NINDS NIH HHS R01 NS084869
6 · The paper itself

Abstract

Mouse embryonic stem (ES) cells are derived from the inner cell mass of the preimplantation embryo and have the developmental capacity to generate all cell types of the body. Combined with efficient genetic manipulation and in vitro differentiation procedures, ES cells are a useful system for the molecular analysis of developmental pathways. We analyzed and compared the transcriptional activities of a cellular polypeptide chain elongation factor 1 alpha (EF), a cellular-virus hybrid (cytomegalo-virus [CMV] immediate early enhancer fused to chicken beta-actin [CBA]), and a viral CMV promoter system in two ES cell lines. When transiently transfected, the EF and CBA promoters robustly drove reporter gene expression, while the CMV promoter was inactive. We also demonstrated that the EF and CBA promoters effectively drove gene expression in different stages of cell development: naïve ES cells, embryoid bodies (EBs), and neuronal precursor cells. In contrast, the CMV promoter did not have transcriptional activity in either ES cells or EB but had significant activity once ES cells differentiated into neuronal precursors. Our data show that individual promoters have different abilities to express reporter gene expression in the ES and other cell types tested.

Indexed as

ActinsAnimalsCell DifferentiationCells, CulturedCytomegalovirusEmbryo, MammalianFemaleGene Expression Regulation, DevelopmentalGenes, Immediate-EarlyGenes, ReporterGreen Fluorescent ProteinsIndicators and ReagentsLuminescent ProteinsMicePeptide Elongation Factor 1Promoter Regions, GeneticActinsGreen Fluorescent ProteinsIndicators and ReagentsLuminescent ProteinsPeptide Elongation Factor 1

Identifiers

PMID11897870
PMCPMC2615228
OpenAlexW2009100845

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.