Evidence map›Paper›PMID 22286130›Full record

ArticleNature chemical biology2012

Spatiotemporal resolution of the Ntla transcriptome in axial mesoderm development.

Ilya A Shestopalov, Cameron L W Pitt, James K Chen

Abstract read
In one paragraph

Article in Nature chemical biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. PhotocleavableChemical reviews · 2023
    Review
  3. Article
  4. Bicyclic Caged Morpholino Oligonucleotides for Optical Gene Silencing.Chembiochem : a European journal of chemical biology · 2022
    Article
  5. Review
  6. Fli1Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. A novel cold-sensitive mutant of ntla reveals temporal roles of brachyury in zebrafish.Developmental dynamics : an official publication of the American Association of Anatomists · 2016
    Article
  13. Article
  14. Caged oligonucleotides for studying biological systems.Journal of inorganic biochemistry · 2015
    Review
  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

3 authors at 1 institution in 1 country.

Ilya A ShestopalovDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, California, USA.
Cameron L W Pitt
James K Chen
Stanford University · US

Funding

Chemical Embryology: Technologies for Manipulating and Visualizing DevelopmentDP1OD003792 · OD · STANFORD UNIVERSITY · PI CHEN, JAMES K · 2008 to 2011
$3.2M
Photochemical Regulation of Embryonic Gene ExpressionR01GM072600 · NIGMS · STANFORD UNIVERSITY · PI CHEN, JAMES K · 2005 to 2009
$1.6M
Deciphering T-box gene-dependent mesoderm development with synthetic probesR01GM087292 · NIGMS · STANFORD UNIVERSITY · PI CHEN, JAMES K · 2010 to 2013
$1.3M
Chemical Embryology: Technologies for Manipulating and Visualizing DevelopmentDP1HD075622 · NICHD · STANFORD UNIVERSITY · PI CHEN, JAMES K · 2012 to 2012
$792k
NICHD NIH HHS DP1 HD075622NIGMS NIH HHS R01 GM072600NIGMS NIH HHS R01 GM087292NIH HHS DP1 OD003792
6 · The paper itself

Abstract

Transcription factors have diverse roles during embryonic development, combinatorially controlling cellular states in a spatially and temporally defined manner. Resolving the dynamic transcriptional profiles that underlie these patterning processes is essential for understanding embryogenesis at the molecular level. Here we show how temporal, tissue-specific changes in embryonic transcription factor function can be discerned by integrating caged morpholino oligonucleotides with photoactivatable fluorophores, fluorescence-activated cell sorting and microarray technologies. As a proof of principle, we have dynamically profiled No tail a (Ntla)-dependent genes at different stages of axial mesoderm development in zebrafish, discovering discrete sets of transcripts that are coincident with either notochord cell fate commitment or differentiation. Our studies reveal new regulators of notochord development and the sequential activation of distinct transcriptomes within a cell lineage by a single transcriptional factor and demonstrate how optically controlled chemical tools can dissect developmental processes with spatiotemporal precision.

Indexed as

Gene Expression Regulation, DevelopmentalTranscriptomeAnimalsBrachyury ProteinFetal ProteinsMesodermT-Box Domain ProteinsTime FactorsZebrafishZebrafish ProteinsBrachyury ProteinFetal ProteinsT-Box Domain ProteinsZebrafish Proteins

Identifiers

PMID22286130
PMCPMC3288381
OpenAlexW2075201827

What OpenQuestion holds

Textmetadata
LicenceTDM
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.