» Articles » PMID: 424299

Precise Location of DNase I Cutting Sites in the Nucleosome Core Determined by High Resolution Gel Electrophoresis

Overview
Specialty Biochemistry
Date 1979 Jan 1
PMID 424299
Citations 59
Authors
Affiliations
Soon will be listed here.
Abstract

The precise locations of the DNase I cutting sites in the nucleosome core have been determined by analysis of the DNA products of a DNase I digestion of 32P end-labelled mucleosome cores on a high resolution gel electrophoresis system. This system is capable of resolving fragments of mixed sequence DNA differing by one base into the region of 160 bases in length. The DNase I cutting sites in the core are found to be spaced at multiples of about 10.4 (i.e. clearly different from 10.0) bases along the DNA, but show significant variations about this value. In addition to the location of the sites, the stagger between individual sites on opposite strands has been determined and is found to be inconsistent with at least one proposed mechanism for nuclease cleavage of chromatin DNA. Finally, a calculated distribution of fragment lengths in a DNase I digest of nuclei has been determined from the data obtained from the nucleosome core and found to be in reasonable agreement with the observed distribution. The periodicity of 10.4 is discussed with respect to the number of base pairs per turn of chromatin DNA and the number of superhelical turns of DNA per nucleosome.

Citing Articles

Nucleosome positions establish an extended mutation signature in melanoma.

Brown A, Mao P, Smerdon M, Wyrick J, Roberts S PLoS Genet. 2018; 14(11):e1007823.

PMID: 30485262 PMC: 6287878. DOI: 10.1371/journal.pgen.1007823.


Intracellular nucleosomes constrain a DNA linking number difference of -1.26 that reconciles the Lk paradox.

Segura J, Joshi R, Diaz-Ingelmo O, Valdes A, Dyson S, Martinez-Garcia B Nat Commun. 2018; 9(1):3989.

PMID: 30266901 PMC: 6162219. DOI: 10.1038/s41467-018-06547-w.


Genomic footprinting.

Vierstra J, Stamatoyannopoulos J Nat Methods. 2016; 13(3):213-21.

PMID: 26914205 DOI: 10.1038/nmeth.3768.


Mapping nucleosome positions using DNase-seq.

Zhong J, Luo K, Winter P, Crawford G, Iversen E, Hartemink A Genome Res. 2016; 26(3):351-64.

PMID: 26772197 PMC: 4772017. DOI: 10.1101/gr.195602.115.


Insertion of the Mu1 transposable element into the first intron of maize Adh1 interferes with transcript elongation but does not disrupt chromatin structure.

Vayda M, Freeling M Plant Mol Biol. 2013; 6(6):441-54.

PMID: 24307421 DOI: 10.1007/BF00027136.


References
1.
Simpson R, Whitlock J . Mapping DNAase l-susceptible sites in nucleosomes labeled at the 5' ends. Cell. 1976; 9(2):347-53. DOI: 10.1016/0092-8674(76)90124-0. View

2.
Felsenfeld G . Chromatin. Nature. 1978; 271(5641):115-22. DOI: 10.1038/271115a0. View

3.
Kornberg R . Structure of chromatin. Annu Rev Biochem. 1977; 46:931-54. DOI: 10.1146/annurev.bi.46.070177.004435. View

4.
Lutter L . Characterization of DNase-I cleavage sites in the nucleosome. Cold Spring Harb Symp Quant Biol. 1978; 42 Pt 1:137-47. DOI: 10.1101/sqb.1978.042.01.015. View

5.
Lutter L . Kinetic analysis of deoxyribonuclease I cleavages in the nucleosome core: evidence for a DNA superhelix. J Mol Biol. 1978; 124(2):391-420. DOI: 10.1016/0022-2836(78)90306-6. View