Evidence map›Paper›PMID 29106413›Full record

ArticleNature structural & molecular biology2017

TFIIH generates a six-base-pair open complex during RNAP II transcription initiation and start-site scanning.

Eric J Tomko, James Fishburn, Steven Hahn, Eric A Galburt

Abstract read
In one paragraph

Article in Nature structural & molecular biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 50 citations in OpenAlex.

  1. The molecular basis of transcription initiation by RNA polymerase II.Nature reviews. Molecular cell biology · 2026
    Review
  2. Article
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  8. Cure and Long-Term Remission Strategies.Methods in molecular biology (Clifton, N.J.) · 2022
    Review
  9. Article
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  14. Single-Molecule Techniques to Study Chromatin.Frontiers in cell and developmental biology · 2021
    Review
  15. Article
  16. Dynamics of RNA polymerase II and elongation factor Spt4/5 recruitment during activator-dependent transcription.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  17. Article
  18. Review
  19. Article
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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

4 authors at 2 institutions in 1 country.

Eric J TomkoBiochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri, USA.
James FishburnDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Steven HahnDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.ORCID http://orcid.org/0000-0001-7240-2533
Eric A GalburtBiochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri, USA.ORCID http://orcid.org/0000-0003-4314-3215
Fred Hutch Cancer Center · USWashington University in St. Louis · US

Funding

MOLECULAR ANALYSIS OF RNAPIII TRANSCRIPTION INITIATIONR01GM053451 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HAHN, STEVEN M · 1995 to 2020
$11.4M
MECHANISMS OF EUKARYOTIC TRANSCRIPTION INITIATIONR01GM120559 · NIGMS · WASHINGTON UNIVERSITY · PI GALBURT, ERIC A · 2016 to 2019
$1.3M
NIGMS NIH HHS R01 GM053451NIGMS NIH HHS R01 GM120559
6 · The paper itself

Abstract

Eukaryotic mRNA transcription initiation is directed by the formation of the megadalton-sized preinitiation complex (PIC). After PIC formation, double-stranded DNA (dsDNA) is unwound to form a single-stranded DNA bubble, and the template strand is loaded into the polymerase active site. DNA opening is catalyzed by Ssl2 (XPB), the dsDNA translocase subunit of the basal transcription factor TFIIH. In yeast, transcription initiation proceeds through a scanning phase during which downstream DNA is searched for optimal start sites. Here, to test models for initial DNA opening and start-site scanning, we measure the DNA-bubble sizes generated by Saccharomyces cerevisiae PICs in real time using single-molecule magnetic tweezers. We show that ATP hydrolysis by Ssl2 opens a 6-base-pair (bp) bubble that grows to 13 bp in the presence of NTPs. These observations support a two-step model wherein ATP-dependent Ssl2 translocation leads to a 6-bp open complex that RNA polymerase II expands via NTP-dependent RNA transcription.

Indexed as

Catalytic DomainDNA HelicasesPromoter Regions, GeneticRNA Polymerase IISaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTranscription Factors, TFIITranscription Factor TFIIBTranscription Factor TFIIHTranscription Initiation, GeneticTranscription Initiation SiteDNA HelicasesRNA Polymerase IISaccharomyces cerevisiae ProteinsSSL2 protein, S cerevisiaeSUA7 protein, S cerevisiaeTranscription Factors, TFIITranscription Factor TFIIBtranscription factor TFIIFTranscription Factor TFIIH

Identifiers

PMID29106413
PMCPMC5741190
OpenAlexW2767091563

What OpenQuestion holds

Textmetadata
LicenceTDM
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.