Evidence map›Paper›PMID 25372608›Full record

ArticlePloS one2014

Isolation of specific neurons from C. elegans larvae for gene expression profiling.

W Clay Spencer, Rebecca McWhirter, Tyne Miller, Pnina Strasbourger, Owen Thompson, LaDeana W Hillier, Robert H Waterston, David M Miller

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing 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

60 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
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  7. A gene expression atlas of a juvenile nervous system.bioRxiv : the preprint server for biology · 2025
    Article
  8. Article
  9. Article
  10. Review
  11. Single-tissue proteomics inProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Article
  13. Article
  14. MAB-5/Hox regulates the Q neuroblast transcriptome, includingbioRxiv : the preprint server for biology · 2023
    Article
  15. A molecular atlas of adultbioRxiv : the preprint server for biology · 2023
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

8 authors.

W Clay SpencerDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, Tennessee, United States of America.
Rebecca McWhirterDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, Tennessee, United States of America.
Tyne MillerProgram in Neuroscience, Vanderbilt University, Nashville, Tennessee, United States of America.
Pnina StrasbourgerDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, Washington, United States of America.
Owen ThompsonDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, Washington, United States of America.
LaDeana W HillierDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, Washington, United States of America.
Robert H WaterstonDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, Washington, United States of America.
David M MillerDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, Tennessee, United States of America; Program in Neuroscience, Vanderbilt University, Nashville, Tennessee, United States of America.

Funding

Project 6 Interactions of Serotonin and Circadian Signaling NetworksP50MH078028 · NIMH · VANDERBILT UNIVERSITY · PI SNODDY, JAY R · 2007 to 2011
$9.8M
Global Identification of transcribed elements in the C. elegans genomeU01HG004263 · NHGRI · UNIVERSITY OF WASHINGTON · PI WATERSTON, ROBERT H · 2007 to 2011
$7.3M
MOLECULAR GENETICS OF NEURAL SPECIFICITYR01NS026115 · NINDS · VANDERBILT UNIVERSITY · PI MILLER, DAVID M · 1994 to 2010
$3.0M
NHGRI NIH HHS U01 HG004263NIMH NIH HHS MH078028NIMH NIH HHS P50 MH078028NINDS NIH HHS R01 NS026115NINDS NIH HHS R01 NS26115
6 · The paper itself

Abstract

backgroundThe simple and well-described structure of the C. elegans nervous system offers an unprecedented opportunity to identify the genetic programs that define the connectivity and function of individual neurons and their circuits. A correspondingly precise gene expression map of C. elegans neurons would facilitate the application of genetic methods toward this goal. Here we describe a powerful new approach, SeqCeL (RNA-Seq of C. elegans cells) for producing gene expression profiles of specific larval C. elegans neurons. METHODS AND

resultsWe have exploited available GFP reporter lines for FACS isolation of specific larval C. elegans neurons for RNA-Seq analysis. Our analysis showed that diverse classes of neurons are accessible to this approach. To demonstrate the applicability of this strategy to rare neuron types, we generated RNA-Seq profiles of the NSM serotonergic neurons that occur as a single bilateral pair of cells in the C. elegans pharynx. These data detected >1,000 NSM enriched transcripts, including the majority of previously known NSM-expressed genes. SIGNIFICANCE: This work offers a simple and robust protocol for expression profiling studies of post-embryonic C. elegans neurons and thus provides an important new method for identifying candidate genes for key roles in neuron-specific development and function.

Indexed as

Caenorhabditis elegansGene Expression ProfilingNeuronsAnimalsCell SeparationGene Expression Regulation

Identifiers

PMID25372608
PMCPMC4221280

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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.