Literature DB >> 627037

Nucleosomal DNA is digested to repeats of 10 bases by exonuclease III.

D Riley, H Weintraub.   

Abstract

Nucleosomes were treated with increasing concentrations of exonuclease III (Exo III) from E. coli. At low levels of Exo III, the heterogeneous distribution of monomers (with associated DNA fragments ranging in size between 140 and 170 bp) is "trimmed" down to a discrete core of 140 bp. The "trimming" of monomers to 140 bp results from a 3' exonucleolytic digestion accompanied by a 5' clipping activity which is specific for the conformation of internucleosomal DNA. At higher concentrations of Exo III, the enzyme digests the 140 bp "trimmed" nucleosome core from both 3' ends without associated 5' nuclease activity. Most striking is the observation that the fragments produced during such a digestion display discrete single-stranded lengths that are integer multiples of 10 bases. For some dimer nucleosomes, Exo III can digest as many as 200 bases from at least one 3' end and produce a 10 base interval ladder from about 400 bases down to 180 bases. This suggests that the enzyme can traverse the length of an entire nucleosome without destroying whatever structural features are necessary to produce a 10 base DNA ladder.

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Year:  1978        PMID: 627037     DOI: 10.1016/0092-8674(78)90197-6

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  30 in total

1.  Nucleoprotein hybridization: a method for isolating active and inactive genes as chromatin.

Authors:  C Vincenz; J Fronk; G A Tank; J P Langmore
Journal:  Nucleic Acids Res       Date:  1991-03-25       Impact factor: 16.971

2.  Studies on the binding of lambda Int protein to attachment site DNA: identification of a tight-binding site in the P' region.

Authors:  R W Davies; P H Schreier; M L Kotewicz; H Echols
Journal:  Nucleic Acids Res       Date:  1979-12-20       Impact factor: 16.971

3.  The promoter and enhancer of the inactive chicken beta-globin gene contains precisely positioned nucleosomes.

Authors:  R Buckle; M Balmer; A Yenidunya; J Allan
Journal:  Nucleic Acids Res       Date:  1991-03-25       Impact factor: 16.971

4.  Unique translational positioning of nucleosomes on synthetic DNAs.

Authors:  D J Fitzgerald; J N Anderson
Journal:  Nucleic Acids Res       Date:  1998-06-01       Impact factor: 16.971

5.  Comparison on the structure and transcriptional capability of growing phase and stationary yeast chromatin: a model for reversible gene activation.

Authors:  D Lohr; G Ide
Journal:  Nucleic Acids Res       Date:  1979       Impact factor: 16.971

6.  Nucleosome packing in chromatin as revealed by nuclease digestion.

Authors:  V A Pospelov; S B Svetlikova; V I Vorob'ev
Journal:  Nucleic Acids Res       Date:  1979-01       Impact factor: 16.971

7.  Cromatin and core particles formed from the inner histones and synthetic polydeoxyribonucleotides of defined sequence.

Authors:  R T Simpson; P Künzler
Journal:  Nucleic Acids Res       Date:  1979-04       Impact factor: 16.971

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

Authors:  Tatiana Nikitina; Difei Wang; Misha Gomberg; Sergei A Grigoryev; Victor B Zhurkin
Journal:  J Mol Biol       Date:  2013-02-28       Impact factor: 5.469

9.  CAG/CTG repeats alter the affinity for the histone core and the positioning of DNA in the nucleosome.

Authors:  Catherine B Volle; Sarah Delaney
Journal:  Biochemistry       Date:  2012-11-27       Impact factor: 3.162

10.  Protection of discrete DNA fragments by the complex H1-octamerhistones or H5-octamerhistones after micrococcal nuclease digestion.

Authors:  S Muyldermans; I Lasters; L Wyns; R Hamers
Journal:  Nucleic Acids Res       Date:  1981-08-11       Impact factor: 16.971

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