Evidence map›Paper›PMID 17134498›Full record

ArticleBMC genomics2006

Genome-wide sequence and functional analysis of early replicating DNA in normal human fibroblasts.

Stephanie M Cohen, Terrence S Furey, Norman A Doggett, David G Kaufman

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Replication Timing Aberration ofGlobal medical genetics · 2023
    Article
  3. Submegabase copy number variations arise during cerebral cortical neurogenesis as revealed by single-cell whole-genome sequencing.Proceedings of the National Academy of Sciences of the United States of America · 2018
    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 3 institutions in 1 country.

Stephanie M CohenDepartment of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, North Carolina 27599, USA. stepmi@med.unc.edu
Terrence S Furey
Norman A Doggett
David G Kaufman
University of North Carolina at Chapel Hill · USDuke University · USLos Alamos National Laboratory · US

Funding

CANCER SUSCEPTIBILITY AND S PHASE INITIATION SITESR01CA084493 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KAUFMAN, DAVID G. · 2000 to 2009
$2.5M
EARLY S PHASE REPLICATION SITES AS ENVIRONMENTAL TARGETSR01ES009112 · NIEHS · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI KAUFMAN, DAVID G. · 1998 to 2002
$753k
NCI NIH HHS CA084493NCI NIH HHS R01 CA084493NIEHS NIH HHS ES09112NIEHS NIH HHS R01 ES009112
6 · The paper itself

Abstract

backgroundThe replication of mammalian genomic DNA during the S phase is a highly coordinated process that occurs in a programmed manner. Recent studies have begun to elucidate the pattern of replication timing on a genomic scale. Using a combination of experimental and computational techniques, we identified a genome-wide set of the earliest replicating sequences. This was accomplished by first creating a cosmid library containing DNA enriched in sequences that replicate early in the S phase of normal human fibroblasts. Clone ends were then sequenced and aligned to the human genome.

resultsBy clustering adjacent or overlapping early replicating clones, we identified 1759 "islands" averaging 100 kb in length, allowing us to perform the most detailed analysis to date of DNA characteristics and genes contained within early replicating DNA. Islands are enriched in open chromatin, transcription related elements, and Alu repetitive elements, with an underrepresentation of LINE elements. In addition, we found a paucity of LTR retroposons, DNA transposon sequences, and an enrichment in all classes of tandem repeats, except for dinucleotides.

conclusionAn analysis of genes associated with islands revealed that nearly half of all genes in the WNT family, and a number of genes in the base excision repair pathway, including four of ten DNA glycosylases, were associated with island sequences. Also, we found an overrepresentation of members of apoptosis-associated genes in very early replicating sequences from both fibroblast and lymphoblastoid cells. These data suggest that there is a temporal pattern of replication for some functionally related genes.

Indexed as

Genome, HumanCell ProliferationCells, CulturedChromatinDNADNA Replication TimingFibroblastsGenesGenomic IslandsGenomic LibraryHumansRepetitive Sequences, Nucleic AcidSequence Analysis, DNATranscription, GeneticChromatinDNA

Identifiers

PMID17134498
PMCPMC1702361
OpenAlexW2096320678

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.