Evidence map›Paper›PMID 24457332›Full record

ArticleNature protocols2014

Applying thiouracil tagging to mouse transcriptome analysis.

Leslie Gay, Kate V Karfilis, Michael R Miller, Chris Q Doe, Kryn Stankunas

Abstract read
In one paragraph

Article in Nature protocols, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. eLife · 2019
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Transcriptomic Profiling of Zebrafish Hair Cells Using RiboTag.Frontiers in cell and developmental biology · 2018
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors.

Leslie Gay1] Institute of Molecular Biology, University of Oregon, Eugene, Oregon, USA. [2] Institute of Neuroscience, University of Oregon, Eugene, Oregon, USA. [3] Howard Hughes Medical Institute, University of Oregon, Eugene, Oregon, USA. [4].
Kate V Karfilis1] Institute of Molecular Biology, University of Oregon, Eugene, Oregon, USA. [2].
Michael R Miller1] Institute of Molecular Biology, University of Oregon, Eugene, Oregon, USA. [2] Institute of Neuroscience, University of Oregon, Eugene, Oregon, USA. [3].
Chris Q Doe1] Institute of Molecular Biology, University of Oregon, Eugene, Oregon, USA. [2] Institute of Neuroscience, University of Oregon, Eugene, Oregon, USA. [3] Howard Hughes Medical Institute, University of Oregon, Eugene, Oregon, USA.
Kryn StankunasInstitute of Molecular Biology, University of Oregon, Eugene, Oregon, USA.

Funding

THE ROLE OF TGF-BETA3 IN PALATOGENESISR01DE013085 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KAARTINEN, VESA M · 2001 to 2014
$5.4M
Genetic and Molecular Studies of NeurogenesisR37HD027056 · NICHD · UNIVERSITY OF OREGON · PI DOE, CHRIS Q · 2012 to 2021
$3.0M
Chromatin Regulation of Heart Valve DevelopmentR01HL115294 · NHLBI · UNIVERSITY OF OREGON · PI STANKUNAS, KRYN · 2014 to 2018
$1.8M
Chromatin Remodeling in Cardiovascular DevelopmentR00HL087598 · NHLBI · UNIVERSITY OF OREGON · PI STANKUNAS, KRYN · 2010 to 2012
$747k
Howard Hughes Medical InstituteNHLBI NIH HHS 5R00HL087598NHLBI NIH HHS R00 HL087598NHLBI NIH HHS R01 HL115294NICHD NIH HHS R37 HD027056NIDCR NIH HHS 3R01DE013085NIDCR NIH HHS R01 DE013085
6 · The paper itself

Abstract

Transcriptional profiling is a powerful approach for studying mouse development, physiology and disease models. Here we describe a protocol for mouse thiouracil tagging (TU tagging), a transcriptome analysis technology that includes in vivo covalent labeling, purification and analysis of cell type-specific RNA. TU tagging enables the isolation of RNA from a given cell population of a complex tissue, avoiding transcriptional changes induced by cell isolation trauma, as well as the identification of actively transcribed RNAs and not preexisting transcripts. Therefore, in contrast to other cell-specific transcriptional profiling methods based on the purification of tagged ribosomes or nuclei, TU tagging provides a direct examination of transcriptional regulation. We describe how to (i) deliver 4-thiouracil to transgenic mice to thio-label cell lineage-specific transcripts, (ii) purify TU-tagged RNA and prepare libraries for Illumina sequencing and (iii) follow a straightforward bioinformatics workflow to identify cell type-enriched or differentially expressed genes. Tissue containing TU-tagged RNA can be obtained in 1 d, RNA-seq libraries can be generated within 2 d and, after sequencing, an initial bioinformatics analysis can be completed in 1 additional day.

Indexed as

ThiouracilAnimalsComputational BiologyGene Expression ProfilingMiceMice, TransgenicRNARNAThiouracil

Identifiers

PMID24457332
PMCPMC4112099

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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.