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 Grigoryev, Victor B. Zhurkin

Research output: Contribution to journalArticle

20 Citations (Scopus)

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.

Original languageEnglish (US)
Pages (from-to)1946-1960
Number of pages15
JournalJournal of Molecular Biology
Volume425
Issue number11
DOIs
StatePublished - Jun 12 2013

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Micrococcal Nuclease
Nucleosomes
Digestion
DNA
Chromosome Mapping
exodeoxyribonuclease III
X Ray Crystallography
Histones
Chromatin
Clone Cells

All Science Journal Classification (ASJC) codes

  • Molecular Biology

Cite this

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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.",
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Combined micrococcal nuclease and exonuclease III digestion reveals precise positions of the nucleosome core/linker junctions : Implications for high-resolution nucleosome mapping. / Nikitina, Tatiana; Wang, Difei; Gomberg, Misha; Grigoryev, Sergei; Zhurkin, Victor B.

In: Journal of Molecular Biology, Vol. 425, No. 11, 12.06.2013, p. 1946-1960.

Research output: Contribution to journalArticle

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