Evidence map›Paper›PMID 32917699›Full record

ArticleScience advances2020

Diversification of reprogramming trajectories revealed by parallel single-cell transcriptome and chromatin accessibility sequencing.

Q R Xing, Chadi A El Farran, Pradeep Gautam, Yu Song Chuah, Tushar Warrier, Cheng-Xu Delon Toh, Nam-Young Kang, Shigeki Sugii, Young-Tae Chang, Jian Xu and 5 more

Abstract read
In one paragraph

Article in Science advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

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  19. Metabolic control of induced pluripotency.Frontiers in cell and developmental biology · 2023
    Review
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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

15 authors.

Q R XingEpigenetics and Cell Fates Laboratory, Programme in Stem Cell, Regenerative Medicine and Aging, Institute of Molecular and Cell Biology, A*STAR, Singapore 138673, Singapore.ORCID 0000-0003-1123-0373
Chadi A El FarranEpigenetics and Cell Fates Laboratory, Programme in Stem Cell, Regenerative Medicine and Aging, Institute of Molecular and Cell Biology, A*STAR, Singapore 138673, Singapore.ORCID 0000-0002-9374-103X
Pradeep GautamEpigenetics and Cell Fates Laboratory, Programme in Stem Cell, Regenerative Medicine and Aging, Institute of Molecular and Cell Biology, A*STAR, Singapore 138673, Singapore.ORCID 0000-0002-3689-8380
Yu Song ChuahEpigenetics and Cell Fates Laboratory, Programme in Stem Cell, Regenerative Medicine and Aging, Institute of Molecular and Cell Biology, A*STAR, Singapore 138673, Singapore.
Tushar WarrierEpigenetics and Cell Fates Laboratory, Programme in Stem Cell, Regenerative Medicine and Aging, Institute of Molecular and Cell Biology, A*STAR, Singapore 138673, Singapore.ORCID 0000-0003-4839-5067
Cheng-Xu Delon TohEpigenetics and Cell Fates Laboratory, Programme in Stem Cell, Regenerative Medicine and Aging, Institute of Molecular and Cell Biology, A*STAR, Singapore 138673, Singapore.
Nam-Young KangLaboratory of Bioimaging Probe Development, Singapore Bioimaging Consortium, A*STAR, Singapore 138667, Singapore.ORCID 0000-0001-8477-2021
Shigeki SugiiInstitute of Bioengineering and Nanotechnology, A*STAR, Singapore 138669, Singapore.ORCID 0000-0002-2537-9534
Young-Tae ChangLaboratory of Bioimaging Probe Development, Singapore Bioimaging Consortium, A*STAR, Singapore 138667, Singapore.ORCID 0000-0002-1927-3688
Jian XuDepartment of Biological Sciences, National University of Singapore, Singapore 117558, Singapore.ORCID 0000-0001-6194-6316
James J CollinsInstitute for Medical Engineering and Science, Department of Biological Engineering, and Synthetic Biology Center, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.ORCID 0000-0002-5560-8246
George Q DaleyStem Cell Program, Division of Pediatric Hematology and Oncology, Boston Children's Hospital and Dana-Farber Cancer Institute, Boston, MA 02115, USA.ORCID 0000-0002-6346-5919
Hu LiCenter for Individualized Medicine, Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN 55905, USA. yhloh@imcb.a-star.edu.sg zhanglf@ntu.edu.sg li.hu@mayo.edu.ORCID 0000-0001-5957-5472
Li-Feng ZhangSchool of Biological Sciences, Nanyang Technological University, Singapore 637551, Singapore. yhloh@imcb.a-star.edu.sg zhanglf@ntu.edu.sg li.hu@mayo.edu.ORCID 0000-0003-0917-0017
Yuin-Han LohEpigenetics and Cell Fates Laboratory, Programme in Stem Cell, Regenerative Medicine and Aging, Institute of Molecular and Cell Biology, A*STAR, Singapore 138673, Singapore. yhloh@imcb.a-star.edu.sg zhanglf@ntu.edu.sg li.hu@mayo.edu.ORCID 0000-0002-4715-6454

Funding

Harnessing Molecular Networks of Resilience for Therapeutic Discoveries in ADR01AG061796 · NIA · MAYO CLINIC JACKSONVILLE · PI ERTEKIN-TANER, NILUFER · 2018 to 2022
$5.7M
Capturing the molecular complexity of Alzheimer's disease through the lens of RNA binding proteinsRF1AG056318 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI LI, HU, WOLOZIN, BENJAMIN L · 2018 to 2020
$4.4M
Determinants of pancreatic cancer and malignant melanoma phenotypes in CDKN2A hereditary kindredsR01CA208517 · NCI · MAYO CLINIC ROCHESTER · PI FERNANDEZ-ZAPICO, MARTIN ERNESTO, LI, HU · 2016 to 2020
$2.9M
NCI NIH HHS R01 CA208517NIA NIH HHS R01 AG061796NIA NIH HHS RF1 AG056318
6 · The paper itself

Abstract

Cellular reprogramming suffers from low efficiency especially for the human cells. To deconstruct the heterogeneity and unravel the mechanisms for successful reprogramming, we adopted single-cell RNA sequencing (scRNA-Seq) and single-cell assay for transposase-accessible chromatin (scATAC-Seq) to profile reprogramming cells across various time points. Our analysis revealed that reprogramming cells proceed in an asynchronous trajectory and diversify into heterogeneous subpopulations. We identified fluorescent probes and surface markers to enrich for the early reprogrammed human cells. Furthermore, combinatory usage of the surface markers enabled the fine segregation of the early-intermediate cells with diverse reprogramming propensities. scATAC-Seq analysis further uncovered the genomic partitions and transcription factors responsible for the regulatory phasing of reprogramming process. Binary choice between a FOSL1 and a TEAD4-centric regulatory network determines the outcome of a successful reprogramming. Together, our study illuminates the multitude of diverse routes transversed by individual reprogramming cells and presents an integrative roadmap for identifying the mechanistic part list of the reprogramming machinery.

Indexed as

ChromatinTranscriptomeCellular ReprogrammingDNA-Binding ProteinsHumansMuscle ProteinsSingle-Cell AnalysisTEA Domain Transcription FactorsTranscription FactorsChromatinDNA-Binding ProteinsMuscle ProteinsTEAD4 protein, humanTEA Domain Transcription FactorsTranscription Factors

Identifiers

PMID32917699
PMCPMC7486102

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.