Evidence map›Paper›PMID 27627025›Full record

ArticleJournal of cellular physiology2017

Identifying Nuclear Matrix-Attached DNA Across the Genome.

Jason R Dobson, Deli Hong, A Rasim Barutcu, Hai Wu, Anthony N Imbalzano, Jane B Lian, Janet L Stein, Andre J van Wijnen, Jeffrey A Nickerson, Gary S Stein

Abstract read
In one paragraph

Article in Journal of cellular physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
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  4. Nuclear architecture and the structural basis of mitotic memory.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2023
    Review
  5. Article
  6. FOXO1 and hsa-microRNA-204-5p affect the biologic behavior of MDA-MB-231 breast cancer cells.International journal of clinical and experimental pathology · 2020
    Article
  7. Review
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  9. 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

10 authors at 3 institutions in 1 country.

Jason R DobsonDepartment of Cell and Developmental Biology, University of Massachusetts Medical School, Worcester, Massachusetts.
Deli HongDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont College of Medicine, Burlington, Vermont.
A Rasim BarutcuDepartment of Cell and Developmental Biology, University of Massachusetts Medical School, Worcester, Massachusetts.
Hai WuDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont College of Medicine, Burlington, Vermont.
Anthony N ImbalzanoDepartment of Cell and Developmental Biology, University of Massachusetts Medical School, Worcester, Massachusetts.
Jane B LianDepartment of Cell and Developmental Biology, University of Massachusetts Medical School, Worcester, Massachusetts.
Janet L SteinDepartment of Cell and Developmental Biology, University of Massachusetts Medical School, Worcester, Massachusetts.
Andre J van WijnenDepartments of Orthopedic Surgery and Biochemistry & Molecular Biology, Mayo Clinic, Rochester, Minnesota.
Jeffrey A NickersonDepartment of Cell and Developmental Biology, University of Massachusetts Medical School, Worcester, Massachusetts.
Gary S SteinDepartment of Cell and Developmental Biology, University of Massachusetts Medical School, Worcester, Massachusetts.
University of Vermont · USUniversity of Massachusetts Chan Medical School · USMayo Clinic · US

Funding

SUBNUCLEAR TARGETING OF TRANSCRIPTION FACTORSP01CA082834 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STEIN, GARY S. · 2001 to 2015
$18.4M
Synthesis of Osteocalcin in BoneR37DE012528 · NIDCR · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LIAN, JANE B. · 2008 to 2017
$5.0M
NCI NIH HHS P01 CA082834NIDCR NIH HHS R37 DE012528
6 · The paper itself

Abstract

Experimental approaches to define the relationship between gene expression and nuclear matrix attachment regions (MARs) have given contrasting and method-specific results. We have developed a next generation sequencing strategy to identify MARs across the human genome (MAR-Seq). The method is based on crosslinking chromatin to its nuclear matrix attachment sites to minimize changes during biochemical processing. We used this method to compare nuclear matrix organization in MCF-10A mammary epithelial-like cells and MDA-MB-231 breast cancer cells and evaluated the results in the context of global gene expression (array analysis) and positional enrichment of gene-regulatory histone modifications (ChIP-Seq). In the normal-like cells, nuclear matrix-attached DNA was enriched in expressed genes, while in the breast cancer cells, it was enriched in non-expressed genes. In both cell lines, the chromatin modifications that mark transcriptional activation or repression were appropriately associated with gene expression. Using this new MAR-Seq approach, we provide the first genome-wide characterization of nuclear matrix attachment in mammalian cells and reveal that the nuclear matrix-associated genome is highly cell-context dependent. J. Cell. Physiol. 232: 1295-1305, 2017. © 2016 Wiley Periodicals, Inc.

Indexed as

Genome, HumanBreast NeoplasmsCell LineChromatinCross-Linking ReagentsDNAFemaleFluorescent Antibody TechniqueGene Expression Regulation, NeoplasticHistonesHumansMatrix Attachment RegionsNuclear MatrixOpen Reading FramesReproducibility of ResultsChromatinCross-Linking ReagentsDNAHistones

Identifiers

PMID27627025
PMCPMC5325791
OpenAlexW2520694393

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.