Evidence map›Paper›PMID 23458408›Full record

ArticleJournal of molecular biology2013

Combined micrococcal nuclease and exonuclease III digestion reveals precise positions of the nucleosome core/linker junctions: implications for high-resolution nucleosome mapping.

Tatiana Nikitina, Difei Wang, Misha Gomberg, Sergei A Grigoryev, Victor B Zhurkin

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Tatiana NikitinaLaboratory of Cell Biology, CCR, National Cancer Institute, NIH, Bethesda, MD, USA.
Difei WangLaboratory of Cell Biology, CCR, National Cancer Institute, NIH, Bethesda, MD, USA.
Misha GombergDepartment of Biochemistry and Molecular Biology, Pennsylvania State University College of Medicine, Hershey, PA, USA.
Sergei A GrigoryevDepartment of Biochemistry and Molecular Biology, Pennsylvania State University College of Medicine, Hershey, PA, USA. Electronic address: sag17@psu.edu.
Victor B ZhurkinLaboratory of Cell Biology, CCR, National Cancer Institute, NIH, Bethesda, MD, USA. Electronic address: zhurkin@nih.gov.
National Cancer Institute · USPennsylvania State University · US

Funding

DNA Folding in Chromatin at the Supra-nucleosome LevelZIABC010844 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ZHURKIN, VICTOR · 2009 to 2025
$9.8M
DNA Deformations and Interactions with Transcription FacZ01BC008371 · BC · BASIC SCIENCES · PI ZHURKIN, VICTOR · 1996 to 2006
–
Intramural NIH HHS Z01 BC008371
6 · The paper itself

Abstract

Micrococcal nuclease (MNase) is extensively used in genome-wide mapping of nucleosomes but its preference for AT-rich DNA leads to errors in establishing precise positions of nucleosomes. Here, we show that the MNase digestion of nucleosomes assembled on a strong nucleosome positioning sequence, Widom's clone 601, releases nucleosome cores whose sizes are strongly affected by the linker DNA sequence. Our experiments produced nucleosomal DNA sizes varying between 147 and 155 bp, with positions of the MNase cuts reflecting positions of the A⋅T pairs rather than the nucleosome core/linker junctions determined by X-ray crystallography. Extent of chromatosomal DNA protection by linker histone H1 also depends on the linker DNA sequence. Remarkably, we found that a combined treatment with MNase and exonuclease III (exoIII) overcomes MNase sequence preference producing nucleosomal DNA trimmed symmetrically and precisely at the core/linker junctions regardless of the underlying DNA sequence. We propose that combined MNase/exoIII digestion can be applied to in situ chromatin for unbiased genome-wide mapping of nucleosome positions that is not influenced by DNA sequences at the core/linker junctions. The same approach can be also used for the precise mapping of the extent of linker DNA protection by H1 and other protein factors associated with nucleosome linkers.

Indexed as

Base SequenceDNAExodeoxyribonucleasesMicrococcal NucleaseModels, MolecularMolecular Sequence DataNucleosomesDNAexodeoxyribonuclease IIIExodeoxyribonucleasesMicrococcal NucleaseNucleosomes

Identifiers

PMID23458408
PMCPMC7597529
OpenAlexW2074833980

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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.