Evidence map›Paper›PMID 17848203›Full record

ArticleGenome biology2007

The embryonic muscle transcriptome of Caenorhabditis elegans.

Rebecca M Fox, Joseph D Watson, Stephen E Von Stetina, Joan McDermott, Thomas M Brodigan, Tetsunari Fukushige, Michael Krause, David M Miller

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2007. 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
2.0field-weighted citation impact, top 15% 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, 86 citations in OpenAlex.

  1. Article
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  4. Review
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  10. Unconventional Myosins fromBiomolecules · 2022
    Review
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  12. Molecular lesions in alleles of themicroPublication biology · 2022
    Article
  13. HLH-1 Modulates Muscle Proteostasis DuringFrontiers in cell and developmental biology · 2022
    Article
  14. Article
  15. Article
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  17. Article
  18. Article
  19. Article
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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

8 authors at 3 institutions in 1 country.

Rebecca M FoxDepartment of Cell and Developmental Biology, Vanderbilt University, 465 21st Ave. S., Nashville, TN 37232-8240, USA.
Joseph D Watson
Stephen E Von Stetina
Joan McDermott
Thomas M Brodigan
Tetsunari Fukushige
Michael Krause
David M Miller
Vanderbilt University · USNational Institute of Diabetes and Digestive and Kidney Diseases · USNational Institutes of Health · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
TRANSGENIC MOUSE/ ES CELL SHARES RESOURCESP60DK020593 · NIDDK · VANDERBILT UNIVERSITY · PI MCGUINNESS, OWEN P · 1986 to 2011
$28.1M
Shop Module CoreP30EY008126 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Kevin L Schey · 1989 to 2026
$19.6M
THREE-TIERED PREVENTION MODEL TO BETTER SERVE ALL STUDENP30HD015052 · NICHD · VANDERBILT UNIVERSITY · PI DYKENS, ELISABETH MAY · 1985 to 2014
$18.6M
Training in Fundamental NeuroscienceT32MH064913 · NIMH · VANDERBILT UNIVERSITY · PI IHRIE, REBECCA A, WINDER, DANNY G. · 2001 to 2022
$7.6M
Global Identification of transcribed elements in the C. elegans genomeU01HG004263 · NHGRI · UNIVERSITY OF WASHINGTON · PI WATERSTON, ROBERT H · 2007 to 2011
$7.3M
Training Program in Stem Cell and Regenerative Developmental BiologyT32HD007502 · NICHD · VANDERBILT UNIVERSITY · PI WRIGHT, CHRISTOPHER V · 1997 to 2022
$5.4M
MOLECULAR PHYSIOLOGY OF MEMBRANE TRANSPORT IN C ELEGANSP01DK058212 · NIDDK · VANDERBILT UNIVERSITY · PI STRANGE, KEVIN · 2000 to 2004
$4.0M
MOLECULAR GENETICS OF NEURAL SPECIFICITYR01NS026115 · NINDS · VANDERBILT UNIVERSITY · PI MILLER, DAVID M · 1994 to 2010
$3.0M
Transcriptional Regulation of MyogenesisZ01DK036131 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI KRAUSE, MICHAEL · 2007 to 2008
$845k
Neuronal gene regulation by the synaptic protein RPM-1F31NS049743 · NINDS · VANDERBILT UNIVERSITY · PI WATSON, JOSEPH D · 2004 to 2006
$77k
NCI NIH HHS P30 CA068485NCI NIH HHS P30 CA68485NEI NIH HHS P30 EY008126NEI NIH HHS P30 EY08126NHGRI NIH HHS U01 HG004263NHLBI NIH HHS P01 HL6744NICHD NIH HHS HD15052NICHD NIH HHS P30 HD015052NICHD NIH HHS T32 HD007502NICHD NIH HHS T32 HD07502NIDDK NIH HHS DK58749NIDDK NIH HHS P01 DK058212NIDDK NIH HHS P01 DK58212NIDDK NIH HHS P30 DK058404NIDDK NIH HHS P30 DK58404NIDDK NIH HHS P60 DK020593NIDDK NIH HHS P60 DK20593NIMH NIH HHS T32 MH064913NIMH NIH HHS T32 MH64913NINDS NIH HHS F31 NS043068NINDS NIH HHS F31 NS046293NINDS NIH HHS F31 NS049743NINDS NIH HHS R01 NS026115NINDS NIH HHS R01 NS26115
6 · The paper itself

Abstract

backgroundThe force generating mechanism of muscle is evolutionarily ancient; the fundamental structural and functional components of the sarcomere are common to motile animals throughout phylogeny. Recent evidence suggests that the transcription factors that regulate muscle development are also conserved. Thus, a comprehensive description of muscle gene expression in a simple model organism should define a basic muscle transcriptome that is also found in animals with more complex body plans. To this end, we applied microarray profiling of Caenorhabtidis elegans cells (MAPCeL) to muscle cell populations extracted from developing C. elegans embryos.

resultsWe used fluorescence-activated cell sorting to isolate myo-3::green fluorescent protein (GFP) positive muscle cells, and their cultured derivatives, from dissociated early C. elegans embryos. Microarray analysis identified 7,070 expressed genes, 1,312 of which are enriched in the myo-3::GFP positive cell population relative to the average embryonic cell. The muscle enriched gene set was validated by comparisons with known muscle markers, independently derived expression data, and GFP reporters in transgenic strains. These results confirm the utility of MAPCeL for cell type specific expression profiling and reveal that 60% of these transcripts have human homologs.

conclusionThis study provides a comprehensive description of gene expression in developing C. elegans embryonic muscle cells. The finding that more than half of these muscle enriched transcripts encode proteins with human homologs suggests that mutant analysis of these genes in C. elegans could reveal evolutionarily conserved models of muscle gene function, with ready application to human muscle pathologies.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsCaenorhabditis elegansCell SeparationComputational BiologyDystrophinFlow CytometryGreen Fluorescent ProteinsHumansMuscle ContractionMusclesNeuromuscular JunctionNucleic Acid HybridizationOligonucleotide Array Sequence AnalysisPhylogenyTranscription FactorsDystrophinGreen Fluorescent ProteinsTranscription Factors

Identifiers

PMID17848203
PMCPMC2375026
OpenAlexW2119668326

What OpenQuestion holds

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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.