Evidence map›Paper›PMID 22954660›Full record

ArticleJournal of molecular biology2013

Structural insights into transcriptional repression by noncoding RNAs that bind to human Pol II.

Susanne A Kassube, Jie Fang, Patricia Grob, Petro Yakovchuk, James A Goodrich, Eva Nogales

Abstract read
In one paragraph

Article in Journal of molecular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Mechanism of mammalian transcriptional repression by noncoding RNA.Nature structural & molecular biology · 2025
    Article
  4. Article
  5. Review
  6. Review
  7. TDP-43 regulates transcription at protein-coding genes and Alu retrotransposons.Biochimica et biophysica acta. Gene regulatory mechanisms · 2019
    Article
  8. 7SK-BAF axis controls pervasive transcription at enhancers.Nature structural & molecular biology · 2016
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. 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

6 authors at 4 institutions in 1 country.

Susanne A KassubeBiophysics Graduate Group, University of California, Berkeley, 742 Stanley Hall, Berkeley, CA 94720, USA.
Jie Fang
Patricia Grob
Petro Yakovchuk
James A Goodrich
Eva Nogales
Howard Hughes Medical Institute · USUniversity of Colorado Boulder · USLawrence Berkeley National Laboratory · USUniversity of California, Berkeley · US

Funding

Regulation of RNA polymerase ll by small RNAsR01GM068414 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI GOODRICH, JAMES · 2003 to 2018
$5.1M
Structural Studies of the Eukaryotic Transcription Initiation MachineryR01GM063072 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI NOGALES, EVA · 2001 to 2016
$2.5M
Howard Hughes Medical InstituteNIGMS NIH HHS GM068414NIGMS NIH HHS GM63072NIGMS NIH HHS R01 GM063072NIGMS NIH HHS R01 GM068414
6 · The paper itself

Abstract

Gene transcription is regulated in response to environmental changes and developmental cues. In mammalian cells subjected to stress conditions such as heat shock, transcription of most protein-coding genes decreases, while the transcription of heat shock protein genes increases. Repression involves direct binding to RNA polymerase II (Pol II) of certain noncoding RNAs (ncRNAs) that are upregulated upon heat shock. Another class of ncRNAs is also upregulated and binds to Pol II but does not inhibit transcription. Incorporation of repressive ncRNAs into pre-initiation complexes prevents transcription initiation, while non-repressive ncRNAs are displaced from Pol II by TFIIF. Here, we present cryo-electron microscopy reconstructions of human Pol II in complex with six different ncRNAs from mouse and human. Our structures show that both repressive and non-repressive ncRNAs bind to a conserved binding site within the cleft of Pol II. The site, which is also shared with a previously characterized yeast aptamer, is close to the active center and, thus, in an ideal position to regulate transcription. Importantly, additional RNA elements extend flexibly beyond the docking site. We propose that the differences concerning the repressive activity of the ncRNAs analyzed must be due to the distinct character of these more unstructured, flexible segments of the RNA that emanate from the cleft.

Indexed as

Epigenetic RepressionAnimalsBinding SitesCryoelectron MicroscopyHeat-Shock ResponseHeLa CellsHumansImage Processing, Computer-AssistedMiceProtein ConformationRNA Polymerase IIRNA, UntranslatedSaccharomyces cerevisiaeTranscription Factors, TFIIUp-RegulationRNA Polymerase IIRNA, UntranslatedTranscription Factors, TFIItranscription factor TFIIFCCDcharge-coupled devicecontrast transfer functioncryo-electron microscopycryo-EMCTFEDTAelectron microscopyethylenediaminetetraacetic acidhPol IIhuman Pol IIncRNAnoncoding RNAPDBPICPol IIpre-initiation complexProtein Data BankRNA polymerase IIstructuretranscription regulationyeast Pol IIyPol II

Identifiers

PMID22954660
PMCPMC3556225
OpenAlexW2052295885

What OpenQuestion holds

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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.