Evidence map›Paper›PMID 30061408›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Promoter-mediated diversification of transcriptional bursting dynamics following gene duplication.

Edward Tunnacliffe, Adam M Corrigan, Jonathan R Chubb

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. What makes genes burst.Trends in cell biology · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Unified bursting strategies in ectopic and endogenousbioRxiv : the preprint server for biology · 2024
    Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Actin dynamics in protein homeostasis.Bioscience reports · 2022
    Review
  15. Article
  16. Article
  17. The Nuclear Pore Complex as a Transcription Regulator.Cold Spring Harbor perspectives in biology · 2022
    Review
  18. Article
  19. Review
  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 2 institutions in 1 country.

Edward TunnacliffeMedical Research Council Laboratory for Molecular Cell Biology, University College London, WC1E 6BT London, United Kingdom.
Adam M CorriganMedical Research Council Laboratory for Molecular Cell Biology, University College London, WC1E 6BT London, United Kingdom.
Jonathan R ChubbMedical Research Council Laboratory for Molecular Cell Biology, University College London, WC1E 6BT London, United Kingdom; j.chubb@ucl.ac.uk.
Medical Research Council · GBMRC Laboratory for Molecular Cell Biology · GB

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council MC_U12266BWellcome TrustWellcome Trust 202867/Z/16/Z
6 · The paper itself

Abstract

During the evolution of gene families, functional diversification of proteins often follows gene duplication. However, many gene families expand while preserving protein sequence. Why do cells maintain multiple copies of the same gene? Here we have addressed this question for an actin family with 17 genes encoding an identical protein. The genes have divergent flanking regions and are scattered throughout the genome. Surprisingly, almost the entire family showed similar developmental expression profiles, with their expression also strongly coupled in single cells. Using live cell imaging, we show that differences in gene expression were apparent over shorter timescales, with family members displaying different transcriptional bursting dynamics. Strong "bursty" behaviors contrasted steady, more continuous activity, indicating different regulatory inputs to individual actin genes. To determine the sources of these different dynamic behaviors, we reciprocally exchanged the upstream regulatory regions of gene family members. This revealed that dynamic transcriptional behavior is directly instructed by upstream sequence, rather than features specific to genomic context. A residual minor contribution of genomic context modulates the gene OFF rate. Our data suggest promoter diversification following gene duplication could expand the range of stimuli that regulate the expression of essential genes. These observations contextualize the significance of transcriptional bursting.

Indexed as

Gene DuplicationPromoter Regions, GeneticTranscription, GeneticActinsCell LineDictyosteliumGene Expression RegulationActinsDictyosteliumgene familysingle-cell transcriptomicsstochastic gene expressiontranscriptional bursting

Identifiers

PMID30061408
PMCPMC6099902
OpenAlexW2885906426

What OpenQuestion 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 OpenQuestion graph.