Evidence map›Paper›PMID 31216470›Full record

ArticleCell reports2019

Rational Reprogramming of Cellular States by Combinatorial Perturbation.

Jialei Duan, Boxun Li, Minoti Bhakta, Shiqi Xie, Pei Zhou, Nikhil V Munshi, Gary C Hon

Abstract read
In one paragraph

Article in Cell reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. The peripheral Atf3Acta biochimica et biophysica Sinica · 2025
    Article
  7. Direct Cardiac Reprogramming in the Age of Computational Biology.Journal of cardiovascular development and disease · 2024
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Single-Cell Genomics: Catalyst for Cell Fate Engineering.Frontiers in bioengineering and biotechnology · 2021
    Review
  14. Review
  15. Article
  16. 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

7 authors.

Jialei DuanLaboratory of Regulatory Genomics, Cecil H. and Ida Green Center for Reproductive Biology Sciences, Division of Basic Reproductive Biology Research, Department of Obstetrics and Gynecology, Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Boxun LiLaboratory of Regulatory Genomics, Cecil H. and Ida Green Center for Reproductive Biology Sciences, Division of Basic Reproductive Biology Research, Department of Obstetrics and Gynecology, Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Minoti BhaktaDepartment of Molecular Biology, Department of Internal Medicine, Division of Cardiology, McDermott Center for Human Growth and Development, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Shiqi XieLaboratory of Regulatory Genomics, Cecil H. and Ida Green Center for Reproductive Biology Sciences, Division of Basic Reproductive Biology Research, Department of Obstetrics and Gynecology, Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Pei ZhouLaboratory of Regulatory Genomics, Cecil H. and Ida Green Center for Reproductive Biology Sciences, Division of Basic Reproductive Biology Research, Department of Obstetrics and Gynecology, Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Nikhil V MunshiDepartment of Molecular Biology, Department of Internal Medicine, Division of Cardiology, McDermott Center for Human Growth and Development, UT Southwestern Medical Center, Dallas, TX 75390, USA; Hamon Center for Regenerative Science and Medicine, Dallas, TX 75390, USA. Electronic address: nikhil.munshi@utsouthwestern.edu.
Gary C HonLaboratory of Regulatory Genomics, Cecil H. and Ida Green Center for Reproductive Biology Sciences, Division of Basic Reproductive Biology Research, Department of Obstetrics and Gynecology, Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Hamon Center for Regenerative Science and Medicine, Dallas, TX 75390, USA. Electronic address: gary.hon@utsouthwestern.edu.

Funding

Combinatorial Biology of Gene Regulation for Cellular EngineeringDP2GM128203 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI HON, GARY CHUNG · 2017 to 2021
$2.9M
Diversity Supplement- Analysis of transcriptional and chromatin accessibility during atrioventricular node formatR01HL136604 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI MUNSHI, NIKHIL VILAS · 2017 to 2021
$2.1M
Diversity Supplement - Magid MohamedR03HL133642 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI MUNSHI, NIKHIL VILAS · 2016 to 2017
$284k
Defining process control parameters for cardiac reprogrammingR03HL135217 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI MUNSHI, NIKHIL VILAS · 2016 to 2017
$162k
NHLBI NIH HHS R01 HL136604NHLBI NIH HHS R03 HL133642NHLBI NIH HHS R03 HL135217NIGMS NIH HHS DP2 GM128203
6 · The paper itself

Abstract

Ectopic expression of transcription factors (TFs) can reprogram cell state. However, because of the large combinatorial space of possible TF cocktails, it remains difficult to identify TFs that reprogram specific cell types. Here, we develop Reprogram-Seq to experimentally screen thousands of TF cocktails for reprogramming performance. Reprogram-Seq leverages organ-specific cell-atlas data with single-cell perturbation and computational analysis to predict, evaluate, and optimize TF combinations that reprogram a cell type of interest. Focusing on the cardiac system, we perform Reprogram-Seq on MEFs using an undirected library of 48 cardiac factors and, separately, a directed library of 10 epicardial-related TFs. We identify a combination of three TFs, which efficiently reprogram MEFs to epicardial-like cells that are transcriptionally, molecularly, morphologically, and functionally similar to primary epicardial cells. Reprogram-Seq holds promise to accelerate the generation of specific cell types for regenerative medicine.

Indexed as

Activating Transcription Factor 3AnimalsBasic Helix-Loop-Helix ProteinsCell LineCellular ReprogrammingComputational BiologyEmbryonic Stem CellsFibroblastsGATA6 Transcription FactorGene Expression Regulation, DevelopmentalMicePericardiumRNA-SeqSingle-Cell AnalysisSoftwareTranscription FactorsActivating Transcription Factor 3Atf3 protein, mouseBasic Helix-Loop-Helix ProteinsGata6 protein, mouseGATA6 Transcription FactorHand2 protein, mouseTranscription Factorscardiaccellular reprogrammingsingle-cell perturbationsingle-cell RNA-Seqtranscription factor

Identifiers

PMID31216470
PMCPMC6667192

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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.