Evidence map›Paper›PMID 31064989›Full record

ArticleNature communications2019

TFIIE orchestrates the recruitment of the TFIIH kinase module at promoter before release during transcription.

Emmanuel Compe, Carlos M Genes, Cathy Braun, Frederic Coin, Jean-Marc Egly

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. 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
3.0field-weighted citation impact, top 8% 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, 57 citations in OpenAlex.

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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

5 authors at 4 institutions in 1 country.

Emmanuel CompeDepartment of Functional Genomics and Cancer, IGBMC, CNRS/INSERM/University of Strasbourg, BP 163, 67404, Illkirch Cedex, C. U. Strasbourg, France. compe@igbmc.fr.
Carlos M GenesDepartment of Functional Genomics and Cancer, IGBMC, CNRS/INSERM/University of Strasbourg, BP 163, 67404, Illkirch Cedex, C. U. Strasbourg, France.
Cathy BraunDepartment of Functional Genomics and Cancer, IGBMC, CNRS/INSERM/University of Strasbourg, BP 163, 67404, Illkirch Cedex, C. U. Strasbourg, France.
Frederic CoinDepartment of Functional Genomics and Cancer, IGBMC, CNRS/INSERM/University of Strasbourg, BP 163, 67404, Illkirch Cedex, C. U. Strasbourg, France.
Jean-Marc EglyDepartment of Functional Genomics and Cancer, IGBMC, CNRS/INSERM/University of Strasbourg, BP 163, 67404, Illkirch Cedex, C. U. Strasbourg, France. egly@igbmc.fr.
Institut de génétique et de biologie moléculaire et cellulaire · FRCentre National de la Recherche Scientifique · FRInserm · FRUniversité de Strasbourg · FR

Funding

TRIGGERING MECHANISMS FOR MIGRANINE HEADACHER03TW006824 · FIC · MASSACHUSETTS GENERAL HOSPITAL · PI MICHAEL, MOSKOWITZ A · 2004 to 2006
$102k
Centre National de la Recherche Scientifique (National Center for Scientific Research) PICS-6824Fondation ARC pour la Recherche sur le Cancer (ARC Foundation for Cancer Research) 130607082Institut National Du Cancer (French National Cancer Institute) INCA-PLBIO17-043Ligue Contre le Cancer (Equipe labélisée 2019)
6 · The paper itself

Abstract

In eukaryotes, the general transcription factors TFIIE and TFIIH assemble at the transcription start site with RNA Polymerase II. However, the mechanism by which these transcription factors incorporate the preinitiation complex and coordinate their action during RNA polymerase II transcription remains elusive. Here we show that the TFIIEα and TFIIEβ subunits anchor the TFIIH kinase module (CAK) within the preinitiation complex. In addition, we show that while RNA polymerase II phosphorylation and DNA opening occur, CAK and TFIIEα are released from the promoter. This dissociation is impeded by either ATP-γS or CDK7 inhibitor THZ1, but still occurs when XPB activity is abrogated. Finally, we show that the Core-TFIIH and TFIIEβ are subsequently removed, while elongation factors such as DSIF are recruited. Remarkably, these early transcriptional events are affected by TFIIE and TFIIH mutations associated with the developmental disorder, trichothiodystrophy.

Indexed as

Transcription, GeneticCell Line, TumorCyclin-Dependent Kinase-Activating KinaseCyclin-Dependent KinasesFibroblastsHumansMutationNuclear ProteinsPhosphorylationPromoter Regions, GeneticRNA Polymerase IITranscriptional Elongation FactorsTranscription Factors, TFIITranscription Factor TFIIHTrichothiodystrophy SyndromesCDK7 protein, humanCyclin-Dependent Kinase-Activating KinaseCyclin-Dependent KinasesNuclear ProteinsRNA Polymerase IISUPT5H protein, humanTranscriptional Elongation FactorsTranscription Factors, TFIItranscription factor TFIIETranscription Factor TFIIH

Identifiers

PMID31064989
PMCPMC6504876
OpenAlexW2944023060

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.