Evidence map›Paper›PMID 21984812›Full record

ArticleJournal of cell science2011

Pulsatile patterns of pituitary hormone gene expression change during development.

Karen Featherstone, Claire V Harper, Anne McNamara, Sabrina Semprini, David G Spiller, Judith McNeilly, Alan S McNeilly, John J Mullins, Michael R H White, Julian R E Davis

Open access · greenAbstract read
In one paragraph

Article in Journal of cell science, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  7. Review
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  9. Article
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  11. Article
  12. It is time to take timing seriously in clinical genetics.European journal of human genetics : EJHG · 2015
    Article
  13. Article
  14. Roles of connexins and pannexins in (neuro)endocrine physiology.Cellular and molecular life sciences : CMLS · 2015
    Review
  15. Review
  16. 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

10 authors at 4 institutions in 1 country.

Karen FeatherstoneDevelopmental Biomedicine Research Group, Faculty of Medical and Human Sciences, AV Hill Building, University of Manchester, Manchester M13 9PT, UK.
Claire V Harper
Anne McNamara
Sabrina Semprini
David G Spiller
Judith McNeilly
Alan S McNeilly
John J Mullins
Michael R H White
Julian R E Davis
University of Liverpool · GBMRC Centre for Reproductive Health · GBThe Queen's Medical Research Institute · GBUniversity of Manchester · GB

Funding

Biotechnology and Biological Sciences Research Council BB/E012965/1Biotechnology and Biological Sciences Research Council BBE0129651Medical Research Council MC_U127685843Wellcome Trust 067252Wellcome Trust 082794
6 · The paper itself

Abstract

Important questions in biology have emerged recently concerning the timing of transcription in living cells. Studies on clonal cell lines have shown that transcription is often pulsatile and stochastic, with implications for cellular differentiation. Currently, information regarding transcriptional activity at cellular resolution within a physiological context remains limited. To investigate single-cell transcriptional activity in real-time in living tissue we used bioluminescence imaging of pituitary tissue from transgenic rats in which luciferase gene expression is driven by a pituitary hormone gene promoter. We studied fetal and neonatal pituitary tissue to assess whether dynamic patterns of transcription change during tissue development. We show that gene expression in single cells is highly pulsatile at the time endocrine cells first appear but becomes stabilised as the tissue develops in early neonatal life. This stabilised transcription pattern might depend upon tissue architecture or paracrine signalling, as isolated cells, generated from enzymatic dispersion of the tissue, display pulsatile luminescence. Nascent cells in embryonic tissue also showed coordinated transcription activity over short distances further indicating that cellular context is important for transcription activity. Overall, our data show that cells alter their patterns of gene expression according to their context and developmental stage, with important implications for cellular differentiation.

Indexed as

Gene Expression Regulation, DevelopmentalPeriodicityAnimalsAnimals, Genetically ModifiedAnimals, NewbornCells, CulturedCellular MicroenvironmentGene Expression ProfilingLuciferases, FireflyLuminescent MeasurementsMorphogenesisPituitary GlandPituitary HormonesPromoter Regions, GeneticRatsLuciferases, FireflyPituitary Hormones

Identifiers

PMID21984812
PMCPMC3196859
OpenAlexW2114493349

What Socratic 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 Socratic graph.