Evidence map›Paper›PMID 24676094›Full record

ArticleGenome research2014

Subtelomeric CTCF and cohesin binding site organization using improved subtelomere assemblies and a novel annotation pipeline.

Nicholas Stong, Zhong Deng, Ravi Gupta, Sufen Hu, Shiela Paul, Amber K Weiner, Evan E Eichler, Tina Graves, Catrina C Fronick, Laura Courtney and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing 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

45 citing papers in PubMed, 81 citations in OpenAlex.

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  6. Genome assembly in the telomere-to-telomere era.Nature reviews. Genetics · 2024
    Review
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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

14 authors at 3 institutions in 1 country.

Nicholas StongGraduate Group in Genomics and Computational Biology, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA; The Wistar Institute, Philadelphia, Pennsylvania 19104, USA;
Zhong DengThe Wistar Institute, Philadelphia, Pennsylvania 19104, USA;
Ravi GuptaThe Wistar Institute, Philadelphia, Pennsylvania 19104, USA;
Sufen HuThe Wistar Institute, Philadelphia, Pennsylvania 19104, USA;
Shiela PaulThe Wistar Institute, Philadelphia, Pennsylvania 19104, USA;
Amber K WeinerThe Wistar Institute, Philadelphia, Pennsylvania 19104, USA;
Evan E EichlerDepartment of Genome Sciences, University of Washington, Seattle, Washington 98195, USA;
Tina GravesThe Genome Institute, Washington University School of Medicine, St. Louis, Missouri 63108, USA.
Catrina C FronickThe Genome Institute, Washington University School of Medicine, St. Louis, Missouri 63108, USA.
Laura CourtneyThe Genome Institute, Washington University School of Medicine, St. Louis, Missouri 63108, USA.
Richard K WilsonThe Genome Institute, Washington University School of Medicine, St. Louis, Missouri 63108, USA.
Paul M LiebermanThe Wistar Institute, Philadelphia, Pennsylvania 19104, USA;
Ramana V DavuluriThe Wistar Institute, Philadelphia, Pennsylvania 19104, USA;
Harold RiethmanThe Wistar Institute, Philadelphia, Pennsylvania 19104, USA;
The Wistar Institute · USWashington University in St. Louis · USUniversity of Washington · US

Funding

Large Scale Genome SequencingU54HG003079 · NHGRI · WASHINGTON UNIVERSITY · PI DUTCHER, SUSAN K · 2004 to 2016
$445.7M
Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
Sequencing and Clone CharacterizationP01HG004120 · NHGRI · UNIVERSITY OF WASHINGTON · PI EICHLER, EVAN · 2007 to 2013
$7.7M
Role of TERRA in Telomere Maintenance and Telomere Stress ResponseR01CA140652 · NCI · WISTAR INSTITUTE · PI LIEBERMAN, PAUL M. · 2010 to 2025
$6.0M
Informatics Platform for Mammalian Gene Regulation at Isoform-levelR01LM011297 · NLM · WISTAR INSTITUTE · PI DAVULURI, RAMANA V · 2013 to 2020
$2.4M
Technology for detection and quantitation of telomeric DNA aberrations in cancerR21CA143349 · NCI · WISTAR INSTITUTE · PI RIETHMAN, HAROLD · 2010 to 2012
$723k
Nanomapping-Assisted Analysis of Human Telomere RegionsR21HG007205 · NHGRI · WISTAR INSTITUTE · PI RIETHMAN, HAROLD, XIAO, MING · 2013 to 2014
$467k
Telomere Characterization of Normal and Cancer Cells Using Next Generation SequenF31HG006395 · NHGRI · UNIVERSITY OF PENNSYLVANIA · PI STONG, NICHOLAS · 2011 to 2014
$132k
NCI NIH HHS P30 CA010815NCI NIH HHS P30 CA060553NCI NIH HHS P30 CA10815NCI NIH HHS R01 CA140652NCI NIH HHS R01CA140652NCI NIH HHS R21 CA143349NCI NIH HHS R21CA143349NHGRI NIH HHS F31 HG006395NHGRI NIH HHS HG004120NHGRI NIH HHS P01 HG004120NHGRI NIH HHS R21 HG007205NHGRI NIH HHS R21HG007205NHGRI NIH HHS U54 HG003079NLM NIH HHS R01 LM011297NLM NIH HHS R01LM011297
6 · The paper itself

Abstract

Mapping genome-wide data to human subtelomeres has been problematic due to the incomplete assembly and challenges of low-copy repetitive DNA elements. Here, we provide updated human subtelomere sequence assemblies that were extended by filling telomere-adjacent gaps using clone-based resources. A bioinformatic pipeline incorporating multiread mapping for annotation of the updated assemblies using short-read data sets was developed and implemented. Annotation of subtelomeric sequence features as well as mapping of CTCF and cohesin binding sites using ChIP-seq data sets from multiple human cell types confirmed that CTCF and cohesin bind within 3 kb of the start of terminal repeat tracts at many, but not all, subtelomeres. CTCF and cohesin co-occupancy were also enriched near internal telomere-like sequence (ITS) islands and the nonterminal boundaries of subtelomere repeat elements (SREs) in transformed lymphoblastoid cell lines (LCLs) and human embryonic stem cell (ES) lines, but were not significantly enriched in the primary fibroblast IMR90 cell line. Subtelomeric CTCF and cohesin sites predicted by ChIP-seq using our bioinformatics pipeline (but not predicted when only uniquely mapping reads were considered) were consistently validated by ChIP-qPCR. The colocalized CTCF and cohesin sites in SRE regions are candidates for mediating long-range chromatin interactions in the transcript-rich SRE region. A public browser for the integrated display of short-read sequence-based annotations relative to key subtelomere features such as the start of each terminal repeat tract, SRE identity and organization, and subtelomeric gene models was established.

Indexed as

Genome, HumanTerminal Repeat SequencesBase SequenceCCCTC-Binding FactorCell Cycle ProteinsCell LineChromosomal Proteins, Non-HistoneCohesinsEmbryonic Stem CellsFibroblastsHumansMolecular Sequence AnnotationMolecular Sequence DataProtein BindingRepressor ProteinsTelomereCCCTC-Binding FactorCell Cycle ProteinsChromosomal Proteins, Non-HistoneCohesinsCTCF protein, humanRepressor Proteins

Identifiers

PMID24676094
PMCPMC4032850
OpenAlexW2074277085

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.