Evidence map›Paper›PMID 30240284›Full record

ArticleEpigenetics2018

A temporal transcriptome and methylome in human embryonic stem cell-derived cardiomyocytes identifies novel regulators of early cardiac development.

Kai Fu, Haruko Nakano, Marco Morselli, Tiffany Chen, Herman Pappoe, Atsuschi Nakano, Matteo Pellegrini

Open access · bronzeAbstract read
In one paragraph

Article in Epigenetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  3. Article
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  8. Human DNA methylation signatures differentiate persistent from resolving MRSA bacteremia.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  9. Article
  10. Secretome Analysis Performed DuringFrontiers in cell and developmental biology · 2020
    Article
  11. Genetic variation of DNA methyltransferase-3A contributes to protection against persistent MRSA bacteremia in patients.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  12. Review
  13. Article
  14. Upregulation of Serum miRNA-3615 Serves as a Biomarker to Predict Disease Onset and Prognosis in Acute Coronary Syndrome Patients.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    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 1 institution in 1 country.

Kai Fua Department of Molecular, Cell, and Developmental Biology , University of California , Los Angeles , CA , USA.ORCID 0000-0002-8107-3556
Haruko Nakanoa Department of Molecular, Cell, and Developmental Biology , University of California , Los Angeles , CA , USA.ORCID 0000-0001-5807-9127
Marco Morsellia Department of Molecular, Cell, and Developmental Biology , University of California , Los Angeles , CA , USA.ORCID 0000-0003-3351-5791
Tiffany Chena Department of Molecular, Cell, and Developmental Biology , University of California , Los Angeles , CA , USA.
Herman Pappoea Department of Molecular, Cell, and Developmental Biology , University of California , Los Angeles , CA , USA.
Atsuschi Nakanoa Department of Molecular, Cell, and Developmental Biology , University of California , Los Angeles , CA , USA.
Matteo Pellegrinia Department of Molecular, Cell, and Developmental Biology , University of California , Los Angeles , CA , USA.
University of California, Los Angeles · US

Funding

Metabolic regulation of heart formationR01HL142801 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI NAKANO, ATSUSHI · 2019 to 2022
$1.6M
Hemogenic endocardium: contribution to the valvular tissue macrophagesR01HL127427 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI NAKANO, ATSUSHI · 2016 to 2019
$1.5M
The role of electromechanical cue on cardiomyocyte maturationR21HL124503 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GIMZEWSKI, JAMES K, NAKANO, ATSUSHI · 2015 to 2016
$407k
NHLBI NIH HHS R01 HL127427NHLBI NIH HHS R01 HL142801NHLBI NIH HHS R21 HL124503
6 · The paper itself

Abstract

Stem cell-based cardiogenesis has become a powerful tool to enhance our understanding of cardiac development and test novel therapeutics for cardiovascular diseases. However, transcriptional and epigenetic regulation of multiple transitional stages from pluripotent cells to committed cardiomyocytes has not yet been fully characterized. To characterize how transcription factors, lincRNAs and DNA methylation change at temporal developmental stages, and identify potential novel regulators during cardiogenesis. We utilized a previously reported protocol that yields human cardiomyocytes (hCM) with more than 90% purity from human Embryonic Stem Cells (hESC). Leveraging the purity of cells resulting from this protocol, we systematically examined how gene expression and DNA methylation programs change at temporal developmental stages during cardiogenesis. Our results provide a comprehensive view of expression changes during cardiogenesis that extend previous studies, allowing us to identify key transcription factors as well as lincRNAs that are strongly associated with cardiac differentiation. Moreover, we incorporated a simple but powerful method to screen for novel regulators of cardiogenesis solely based on expression changes and found four novel cardiac-related transcription factors, i.e., SORBS2, MITF, DPF3, and ZNF436, which have no or few prior literature reports and we were able to validate using siRNA. Our strategy of identifying novel regulators of cardiogenesis can also be easily implemented in other stem cell-based systems. Our results provide a valuable resource for understanding cardiogenesis that extends previous findings by leveraging the purity of our cell lines, which allowed us to identify four novel cardiac-related regulators.

Indexed as

DNA MethylationGene Expression Regulation, DevelopmentalTranscriptomeAdaptor Proteins, Signal TransducingCell DifferentiationCells, CulturedDNA-Binding ProteinsHomeodomain ProteinsHuman Embryonic Stem CellsHumansMicrophthalmia-Associated Transcription FactorMyocytes, CardiacRNA-Binding ProteinsTranscription FactorsAdaptor Proteins, Signal TransducingDNA-Binding ProteinsDPF3 protein, humanHomeodomain ProteinsMicrophthalmia-Associated Transcription FactorMITF protein, humanRNA-Binding ProteinsSORBS2 protein, humanTranscription FactorsZNF436 protein, humanCardiac differentiationmethylomestem celltranscription factortranscriptome

Identifiers

PMID30240284
PMCPMC6342070
OpenAlexW2890769067

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.