Evidence map›Paper›PMID 29632207›Full record

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

Live-cell analysis of endogenous GFP-RPB1 uncovers rapid turnover of initiating and promoter-paused RNA Polymerase II.

Barbara Steurer, Roel C Janssens, Bart Geverts, Marit E Geijer, Franziska Wienholz, Arjan F Theil, Jiang Chang, Shannon Dealy, Joris Pothof, Wiggert A van Cappellen and 2 more

Abstract 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 136 papers.

0numbers the graph read from it
0cells of the map it votes in
136citing 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

136 citing papers in PubMed.

  1. Review
  2. SEC Mediates mAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  12. bioRxiv : the preprint server for biology · 2026
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  20. Dual Modes of Gene Regulation by CDK12.bioRxiv : the preprint server for biology · 2025
    Article

76 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Barbara SteurerDepartment of Molecular Genetics, Erasmus Medical Center, 3015 AA Rotterdam, The Netherlands.
Roel C JanssensDepartment of Molecular Genetics, Erasmus Medical Center, 3015 AA Rotterdam, The Netherlands.
Bart GevertsDepartment of Pathology, Optical Imaging Centre, Erasmus Medical Center, 3015 AA Rotterdam, The Netherlands.
Marit E GeijerDepartment of Molecular Genetics, Erasmus Medical Center, 3015 AA Rotterdam, The Netherlands.
Franziska WienholzDepartment of Molecular Genetics, Erasmus Medical Center, 3015 AA Rotterdam, The Netherlands.
Arjan F TheilDepartment of Molecular Genetics, Erasmus Medical Center, 3015 AA Rotterdam, The Netherlands.
Jiang ChangDepartment of Molecular Genetics, Erasmus Medical Center, 3015 AA Rotterdam, The Netherlands.
Shannon DealyDepartment of Molecular Genetics, Erasmus Medical Center, 3015 AA Rotterdam, The Netherlands.
Joris PothofDepartment of Molecular Genetics, Erasmus Medical Center, 3015 AA Rotterdam, The Netherlands.
Wiggert A van CappellenDepartment of Pathology, Optical Imaging Centre, Erasmus Medical Center, 3015 AA Rotterdam, The Netherlands.
Adriaan B HoutsmullerDepartment of Pathology, Optical Imaging Centre, Erasmus Medical Center, 3015 AA Rotterdam, The Netherlands.
Jurgen A MarteijnDepartment of Molecular Genetics, Erasmus Medical Center, 3015 AA Rotterdam, The Netherlands; J.Marteijn@erasmusmc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Initiation and promoter-proximal pausing are key regulatory steps of RNA Polymerase II (Pol II) transcription. To study the in vivo dynamics of endogenous Pol II during these steps, we generated fully functional GFP-RPB1 knockin cells. GFP-RPB1 photobleaching combined with computational modeling revealed four kinetically distinct Pol II fractions and showed that on average 7% of Pol II are freely diffusing, while 10% are chromatin-bound for 2.4 seconds during initiation, and 23% are promoter-paused for only 42 seconds. This unexpectedly high turnover of Pol II at promoters is most likely caused by premature termination of initiating and promoter-paused Pol II and is in sharp contrast to the 23 minutes that elongating Pol II resides on chromatin. Our live-cell-imaging approach provides insights into Pol II dynamics and suggests that the continuous release and reinitiation of promoter-bound Pol II is an important component of transcriptional regulation.

Indexed as

Cell Line, TransformedGene Knock-In TechniquesGreen Fluorescent ProteinsHumansPromoter Regions, GeneticRecombinant Fusion ProteinsRNA Polymerase IITranscription, GeneticGreen Fluorescent ProteinsRecombinant Fusion ProteinsRNA Polymerase IIlive-cell imagingpromoter-proximal pausingRNA Polymerase IItranscriptiontranscription dynamics

Identifiers

PMID29632207
PMCPMC5948963

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.