Literature DB >> 9153300

Distribution of topoisomerase II-mediated cleavage sites and relation to structural and functional landmarks in 830 kb of Drosophila DNA.

R Miassod1, S V Razin, R Hancock.   

Abstract

The pattern of sites for cleavage mediated by topoisomerase II was determined in 830 kb of cloned DNA from the Drosophila X chromosome, with the objectives of comparing it with mapped structural and functional landmarks and examining if the correlations with such landmarks reported in individual loci can be generalized to a region approximately 100 times longer. The relative frequencies of topoisomerase II cleavage sites in 247 restriction fragments from 67 clones were quantified by hybridization with probes prepared from DNA fragments which abutted all cleavage sites in each clone, selected through the covalently bound topoisomerase II subunit; the specificity and quantitative nature of this method were demonstrated using a plasmid DNA model. The 12 restriction fragments with strong nuclear scaffold attachment (SAR) activity, of which seven possess autonomous replication (ARS) activity, show statistically strong coincidence or contiguity ( P </=0.11) with regions of high topoisomerase II cleavage site frequency. These regions show no correlation with repetitive sequence or A/T or C/G content and some extend over >10 kb; their sensitivity is therefore unlikely to be due to alternating purine-pyrimidine repeats or regions of Z conformation, which are preferred motifs. The hypothesis that they possess intrinsic curvature is consistent with the similarity of their length and spacing to regions of predicted curvature in the 315 kb DNA of Saccharomyces cerevisiae chromosome III and with the reported strong binding preference of topoisomerase II for curved DNA. The topoisomerase II cleavage pattern in this DNA further shows that its relationships to functional properties seen in individual loci, especially to MAR/SAR and ARS activity and to the restricted accessibility of DNA to topoisomerase II in vivo, can be generalized to much longer regions of the genome.

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Year:  1997        PMID: 9153300      PMCID: PMC146713          DOI: 10.1093/nar/25.11.2041

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  49 in total

1.  Drosophila topoisomerase II double-strand DNA cleavage: analysis of DNA sequence homology at the cleavage site.

Authors:  M Sander; T S Hsieh
Journal:  Nucleic Acids Res       Date:  1985-02-25       Impact factor: 16.971

2.  The 87A7 chromomere. Identification of novel chromatin structures flanking the heat shock locus that may define the boundaries of higher order domains.

Authors:  A Udvardy; E Maine; P Schedl
Journal:  J Mol Biol       Date:  1985-09-20       Impact factor: 5.469

3.  Chromosomal loop anchorage of the kappa immunoglobulin gene occurs next to the enhancer in a region containing topoisomerase II sites.

Authors:  P N Cockerill; W T Garrard
Journal:  Cell       Date:  1986-01-31       Impact factor: 41.582

4.  Detection, sequence patterns and function of unusual DNA structures.

Authors:  J N Anderson
Journal:  Nucleic Acids Res       Date:  1986-11-11       Impact factor: 16.971

5.  A consensus sequence for cleavage by vertebrate DNA topoisomerase II.

Authors:  J R Spitzner; M T Muller
Journal:  Nucleic Acids Res       Date:  1988-06-24       Impact factor: 16.971

6.  In vivo localization of DNA topoisomerase II cleavage sites on Drosophila heat shock chromatin.

Authors:  T C Rowe; J C Wang; L F Liu
Journal:  Mol Cell Biol       Date:  1986-04       Impact factor: 4.272

7.  Topoisomerase II cleavage in chromatin.

Authors:  A Udvardy; P Schedl; M Sander; T S Hsieh
Journal:  J Mol Biol       Date:  1986-09-20       Impact factor: 5.469

8.  Mammalian DNA enriched for replication origins is enriched for snap-back sequences.

Authors:  M Zannis-Hadjopoulos; G Kaufmann; R G Martin
Journal:  J Mol Biol       Date:  1984-11-15       Impact factor: 5.469

9.  Human 170 kDa and 180 kDa topoisomerases II bind preferentially to curved and left-handed linear DNA.

Authors:  T Bechert; S Diekmann; D J Arndt-Jovin
Journal:  J Biomol Struct Dyn       Date:  1994-12

10.  DNA topoisomerase II cleaves at specific sites in the 5' flanking region of c-fos proto-oncogenes in vitro.

Authors:  M K Darby; R E Herrera; H P Vosberg; A Nordheim
Journal:  EMBO J       Date:  1986-09       Impact factor: 11.598

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  6 in total

1.  The matrix attachment region in the Chinese hamster dihydrofolate reductase origin of replication may be required for local chromatid separation.

Authors:  L D Mesner; J L Hamlin; P A Dijkwel
Journal:  Proc Natl Acad Sci U S A       Date:  2003-03-10       Impact factor: 11.205

2.  DNA topoisomerase II sites in the histone H4 gene during the highly synchronous cell cycle of Physarum polycephalum.

Authors:  V Borde; M Duguet
Journal:  Nucleic Acids Res       Date:  1998-05-01       Impact factor: 16.971

3.  Selection of DNA Cleavage Sites by Topoisomerase II Results from Enzyme-Induced Flexibility of DNA.

Authors:  Yunsu Jang; Heyjin Son; Sang-Wook Lee; Wonseok Hwang; Seung-Ryoung Jung; Jo Ann W Byl; Neil Osheroff; Sanghwa Lee
Journal:  Cell Chem Biol       Date:  2019-01-31       Impact factor: 8.116

4.  Distinct frequency-distributions of homopolymeric DNA tracts in different genomes.

Authors:  K J Dechering; K Cuelenaere; R N Konings; J A Leunissen
Journal:  Nucleic Acids Res       Date:  1998-09-01       Impact factor: 16.971

5.  Induction of unique structural changes in guanine-rich DNA regions by the triazoloacridone C-1305, a topoisomerase II inhibitor with antitumor activities.

Authors:  Krzysztof Lemke; Marcin Wojciechowski; William Laine; Christian Bailly; Pierre Colson; Maciej Baginski; Annette K Larsen; Andrzej Skladanowski
Journal:  Nucleic Acids Res       Date:  2005-10-27       Impact factor: 16.971

6.  DNA topoisomerase II selects DNA cleavage sites based on reactivity rather than binding affinity.

Authors:  Felix Mueller-Planitz; Daniel Herschlag
Journal:  Nucleic Acids Res       Date:  2007-05-21       Impact factor: 16.971

  6 in total

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