Evidence map›Paper›PMID 26429969›Full record

ArticleNucleic acids research2016

Genome-wide profiling of nucleosome sensitivity and chromatin accessibility in Drosophila melanogaster.

Răzvan V Chereji, Tsung-Wai Kan, Magda K Grudniewska, Alexander V Romashchenko, Eugene Berezikov, Igor F Zhimulev, Victor Guryev, Alexandre V Morozov, Yuri M Moshkin

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2016. 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
5.7field-weighted citation impact, top 3% 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

45 citing papers in PubMed, 82 citations in OpenAlex.

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  17. Peculiarities ofInternational journal of molecular sciences · 2021
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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

9 authors at 6 institutions in 3 countries.

Răzvan V CherejiProgram in Genomics of Differentiation, Eunice Kennedy Shriver National Institute for Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Tsung-Wai KanDepartment of Biochemistry, Erasmus Medical Center, P.O. Box 2040, 3000 CA Rotterdam, The Netherlands.
Magda K GrudniewskaEuropean Research Institute for the Biology of Ageing, University of Groningen, University Medical Center Groningen, Groningen, 9713AD, The Netherlands.
Alexander V RomashchenkoInstitute of Cytology and Genetics, Siberian Branch of RAS, Novosibirsk 630090, Russia.
Eugene BerezikovEuropean Research Institute for the Biology of Ageing, University of Groningen, University Medical Center Groningen, Groningen, 9713AD, The Netherlands.
Igor F ZhimulevInstitute of Molecular and Cellular Biology, Siberian Branch of RAS, Novosibirsk 630090, Russia.
Victor GuryevEuropean Research Institute for the Biology of Ageing, University of Groningen, University Medical Center Groningen, Groningen, 9713AD, The Netherlands.
Alexandre V MorozovDepartment of Physics and Astronomy and BioMaPS Institute for Quantitative Biology, Rutgers University, Piscataway, NJ 08854, USA morozov@physics.rutgers.edu.
Yuri M MoshkinDepartment of Biochemistry, Erasmus Medical Center, P.O. Box 2040, 3000 CA Rotterdam, The Netherlands Institute of Cytology and Genetics, Siberian Branch of RAS, Novosibirsk 630090, Russia Institute of Molecular and Cellular Biology, Siberian Branch of RAS, Novosibirsk 630090, Russia yury.moshkin@gmail.com.
University of Groningen · NLErasmus MC · NLEunice Kennedy Shriver National Institute of Child Health and Human Development · USInstitute of Cytology and Genetics · RUInstitute of Molecular and Cell Biology · RUUniversity Medical Center Groningen · NL

Funding

Biophysical Models for Prediction and Design of Eukaryotic Chromatin Structure anR01HG004708 · NHGRI · RUTGERS, THE STATE UNIV OF N.J. · PI MOROZOV, ALEXANDRE V · 2009 to 2012
$1.1M
NHGRI NIH HHS R01 HG004708
6 · The paper itself

Abstract

Nucleosomal DNA is thought to be generally inaccessible to DNA-binding factors, such as micrococcal nuclease (MNase). Here, we digest Drosophila chromatin with high and low concentrations of MNase to reveal two distinct nucleosome types: MNase-sensitive and MNase-resistant. MNase-resistant nucleosomes assemble on sequences depleted of A/T and enriched in G/C-containing dinucleotides, whereas MNase-sensitive nucleosomes form on A/T-rich sequences found at transcription start and termination sites, enhancers and DNase I hypersensitive sites. Estimates of nucleosome formation energies indicate that MNase-sensitive nucleosomes tend to be less stable than MNase-resistant ones. Strikingly, a decrease in cell growth temperature of about 10°C makes MNase-sensitive nucleosomes less accessible, suggesting that observed variations in MNase sensitivity are related to either thermal fluctuations of chromatin fibers or the activity of enzymatic machinery. In the vicinity of active genes and DNase I hypersensitive sites nucleosomes are organized into periodic arrays, likely due to 'phasing' off potential barriers formed by DNA-bound factors or by nucleosomes anchored to their positions through external interactions. The latter idea is substantiated by our biophysical model of nucleosome positioning and energetics, which predicts that nucleosomes immediately downstream of transcription start sites are anchored and recapitulates nucleosome phasing at active genes significantly better than sequence-dependent models.

Indexed as

Gene Expression ProfilingGenomeAnimalsChromatinChromatin ImmunoprecipitationDrosophila melanogasterNucleosomesChromatinNucleosomes

Identifiers

PMID26429969
PMCPMC4756854
OpenAlexW2216978877

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.