Skip to content
DraconiticResearch
Search Sources API
203,203 studies31 sourcesUpdated 37 min ago
Peer-reviewedCC BYNature Genetics

Enhancer control of promoter activity and variability via frequency modulation of clustered transcriptional bursts

  1. 1Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland
  2. 2University of Basel, Basel, Switzerland
  3. 3Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland. [email protected]

Abstract

Gene expression in mammalian cells is controlled by enhancers that are often dispersed across large cis-regulatory landscapes around a promoter. How enhancers determine transcription of their target genes and how this depends on their relative position within a cis-regulatory landscape remain unclear. Here we use live-cell imaging to track the activity of a promoter under the control of the same enhancer, but inserted at different positions across a simplified regulatory landscape with minimal complexity. Combined with mathematical modeling, this reveals that RNA production from the promoter occurs in clusters of transcriptional bursts, with enhancer position controlling the frequency at which clusters appear. This results in bursts being more frequent and occurring more uniformly across cells when the enhancer is genomically close to the promoter than when it is located at a large genomic distance. Mathematical modeling further indicates that the enhancer modulates the promoter's ability to transition from its basal transcriptional state to a regime in which clusters of bursts become more frequent. Our results reveal unexplored modes of mammalian promoter operation and show that enhancer position within a cis-regulatory landscape critically controls the timing and variability of transcriptional output in single cells.

Related

  1. A transcriptional cofactor GRIP1 drives PPARγ DNA binding and p300-dependent enhancer activity during homeostatic macrophage polarization
    Marija Dacic, William J Stein, Ruoxi Yuan +5
    Science advancesPeer-reviewedCC BY-NCFull textMolecular biology & gene regulationEurope PMCCrossref
  2. Dynamic merging of enhancer- and promoter-associated assemblies is coupled to transcriptional bursting
    Q. Lin, B. Wang, Y. Liu +9
    bioRxivPreprintAll rights reservedFull textMolecular biology & gene regulationbioRxiv
  3. Enhancer-promoter proximity predicts transcriptional competence but not transcriptional output in the Drosophila brain
    Olivier Messina, Loucif Remini, Christopher H. Bohrer +4
    arXivPreprintCC BY-NC-SA 4.0Full textBiophysicsGenetics & genomicsarXiv
  4. Cumulative transcription factor binding and p300-mediated histone acetylation drive enhancer activation frequency
    Valentina Baderna, Guido Barzaghi, Rozemarijn Kleinendorst +9
    Nature GeneticsPeer-reviewedCC BYFull text9 citedMolecular biology & gene regulationOpenAlex
  5. Analysis of proteasome stress in different cell types defines a conserved transcriptional response signature and its modulation with aging
    Mamta Rai, Yong-Dong Wang, Anna Stephan +2
    G3: Genes | Genomes | GeneticsPeer-reviewedCC BY 4.0Full text1 citedMolecular biology & gene regulationPMC
BibTeX
@article{tunnermann2026enhancer,
  title = {{Enhancer control of promoter activity and variability via frequency modulation of clustered transcriptional bursts}},
  author = {Jana Tünnermann and Grégory Roth and Julie Cramard and Luca Giorgetti},
  journal = {Nature Genetics},
  year = {2026},
  month = jul,
  doi = {10.1038/s41588-026-02676-x},
  url = {https://doi.org/10.1038/s41588-026-02676-x},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Enhancer control of promoter activity and variability via frequency modulation of clustered transcriptional bursts
AU  - Jana Tünnermann
AU  - Grégory Roth
AU  - Julie Cramard
AU  - Luca Giorgetti
PY  - 2026
DA  - 2026/07/14
JO  - Nature Genetics
DO  - 10.1038/s41588-026-02676-x
UR  - https://doi.org/10.1038/s41588-026-02676-x
AB  - Gene expression in mammalian cells is controlled by enhancers that are often dispersed across large cis-regulatory landscapes around a promoter. How enhancers determine transcription of their target genes and how this depends on their relative position within a cis-regulatory landscape remain unclear. Here we use live-cell imaging to track the activity of a promoter under the control of the same enhancer, but inserted at different positions across a simplified regulatory landscape with minimal complexity. Combined with mathematical modeling, this reveals that RNA production from the promoter occurs in clusters of transcriptional bursts, with enhancer position controlling the frequency at which clusters appear. This results in bursts being more frequent and occurring more uniformly across cells when the enhancer is genomically close to the promoter than when it is located at a large genomic distance. Mathematical modeling further indicates that the enhancer modulates the promoter's ability to transition from its basal transcriptional state to a regime in which clusters of bursts become more frequent. Our results reveal unexplored modes of mammalian promoter operation and show that enhancer position within a cis-regulatory landscape critically controls the timing and variability of transcriptional output in single cells.
SN  - 1061-4036
SN  - 1546-1718
ER  -