Evidence map›Paper›PMID 17210645›Full record

ArticleMolecular and cellular biology2007

CTCF interacts with and recruits the largest subunit of RNA polymerase II to CTCF target sites genome-wide.

Igor Chernukhin, Shaharum Shamsuddin, Sung Yun Kang, Rosita Bergström, Yoo-Wook Kwon, Wenqiang Yu, Joanne Whitehead, Rituparna Mukhopadhyay, France Docquier, Dawn Farrar and 8 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

112 citing papers in PubMed, 173 citations in OpenAlex.

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

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

18 authors at 5 institutions in 7 countries.

Igor ChernukhinDepartment of Biological Sciences, Central Campus, University of Essex, Wivenhoe Park, Colchester, Essex CO4 3SQ, United Kingdom.
Shaharum Shamsuddin
Sung Yun Kang
Rosita Bergström
Yoo-Wook Kwon
Wenqiang Yu
Joanne Whitehead
Rituparna Mukhopadhyay
France Docquier
Dawn Farrar
Ian Morrison
Marc Vigneron
Shwu-Yuan Wu
Cheng-Ming Chiang
Dmitri Loukinov
Victor Lobanenkov
Rolf Ohlsson
Elena Klenova
University of Essex · GBUppsala University · SENational Institutes of Health · USUniversity School · USCentre National de la Recherche Scientifique · FR

Funding

E2-Cellular Complexes in HPV Chromatin TranscriptionR01CA103867 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI CHIANG, CHENG-MING · 2004 to 2017
$4.0M
Regulation of p53 Transcription by Viral Oncoproteins & Covalent ModificationsR01CA124760 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI CHIANG, CHENG-MING · 2007 to 2012
$1.6M
Transcriptional Regulation Of Ctcf And Boris ExpressionZ01AI000860 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI LOBANENKOV, VICTOR · 2000 to 2008
$1.5M
Breast Cancer Now 2004NOV45Intramural NIH HHSMedical Research Council G0401088NCI NIH HHS CA103867NCI NIH HHS R01 CA103867NCI NIH HHS R01 CA124760Worldwide Cancer Research 99-0514
6 · The paper itself

Abstract

CTCF is a transcription factor with highly versatile functions ranging from gene activation and repression to the regulation of insulator function and imprinting. Although many of these functions rely on CTCF-DNA interactions, it is an emerging realization that CTCF-dependent molecular processes involve CTCF interactions with other proteins. In this study, we report the association of a subpopulation of CTCF with the RNA polymerase II (Pol II) protein complex. We identified the largest subunit of Pol II (LS Pol II) as a protein significantly colocalizing with CTCF in the nucleus and specifically interacting with CTCF in vivo and in vitro. The role of CTCF as a link between DNA and LS Pol II has been reinforced by the observation that the association of LS Pol II with CTCF target sites in vivo depends on intact CTCF binding sequences. "Serial" chromatin immunoprecipitation (ChIP) analysis revealed that both CTCF and LS Pol II were present at the beta-globin insulator in proliferating HD3 cells but not in differentiated globin synthesizing HD3 cells. Further, a single wild-type CTCF target site (N-Myc-CTCF), but not the mutant site deficient for CTCF binding, was sufficient to activate the transcription from the promoterless reporter gene in stably transfected cells. Finally, a ChIP-on-ChIP hybridization assay using microarrays of a library of CTCF target sites revealed that many intergenic CTCF target sequences interacted with both CTCF and LS Pol II. We discuss the possible implications of our observations with respect to plausible mechanisms of transcriptional regulation via a CTCF-mediated direct link of LS Pol II to the DNA.

Indexed as

Genome, HumanAnimalsBinding SitesBreast NeoplasmsCCCTC-Binding FactorCell Line, TumorCell NucleusChromatin ImmunoprecipitationDNA-Binding ProteinsGenes, ReporterHeLa CellsHumansImmunohistochemistryK562 CellsMiceNIH 3T3 CellsCCCTC-Binding FactorCTCF protein, humanCtcf protein, mouseDNA-Binding ProteinsRepressor ProteinsRNA Polymerase II

Identifiers

PMID17210645
PMCPMC1820452
OpenAlexW2157835438

What OpenQuestion holds

Textmetadata
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.