Matches in SemOpenAlex for { <https://semopenalex.org/work/W1551639504> ?p ?o ?g. }
Showing items 1 to 72 of
72
with 100 items per page.
- W1551639504 endingPage "1086" @default.
- W1551639504 startingPage "1086" @default.
- W1551639504 abstract "Proc Amer Assoc Cancer Res, Volume 47, 20064623 The human genome contains ∼3x103 of hypervariable minisatellites that consist of up to >3 kbp of 85-100% A/T-rich repeats. These unique domains, termed AT islands, tend to overlap with various sites of genomic instability, including cancer relevant fragile sites FRA16B and FRA16D. AT islands are preferentially targeted by an extremely potent DNA-alkylating antitumor drug bizelesin. Computational analysis suggested that DNA duplexes within AT islands are exceptionally destabilized. This property might underlie the unique potential of AT islands to serve as matrix attachment regions (MARs), the vital elements of nuclear organization. Here we use biochemical approaches and atomic force microscopy (AFM) to characterize the duplexes of cloned model AT islands, including a 1076 bp segment of FRA16B AT island. Partially single-stranded nature of AT-island containing plasmids was demonstrated using the single-strand specific P1 nuclease. P1-induced cleavage (resulting in disappearance of superhelical Form I) was profoundly facilitated in AT-island plasmids relative to control plasmids. For example, P1 at 0.2 Units /reaction converted 48% FRA16B AT island plasmid versus only 6% conversion of the vector plasmid. AFM experiments (conducted in dry mode at pH 7.0) revealed presumably single stranded sections in AT island-containing plasmids that were absent from control non-AT island plasmids. In addition, unusual structural features suggestive of hairpin loops (consistent with palindromic sequences present in the FRA16B domain) were observed in FRA16B plasmids. AFM determinations at elevated pH (to facilitate unwinding) further underscored the profound structural differences between AT island and non-AT island plasmids. Single-strand specific replication protein A (RPA) was used as an alternative way to identify DNA unwinding. AFM demonstrated that RPA formed large aggregates with the FRA16B plasmids but not with non-AT island plasmid. Also, RPA binding to AT island sequences was confirmed using electrophoretic mobility shift assay with linear FRA16B DNA and FRA16B supercoiled plasmid. AFM features indicative of single-stranded sections were markedly reduced in bizelesin-treated AT island plasmids. Likewise, pretreatment with bizelesin abrogated the plasmid’s ability to bind RPA. These observations demonstrate that bizelesin distorts the unusual structures of AT islands. While drug binding is expected to stabilize DNA duplex structure, bizelesin effects on AT island plasmids are probably more complex, as bizelesin-treated plasmids retain enhanced sensitivity to P1 nuclease. Demonstration that AT islands are indeed unwound under physiological conditions corroborates the in silico predictions and warrants further investigations on the role of these domains and their variability in chromatin organization in cancer versus normal cells. (Supported by CA80936)" @default.
- W1551639504 created "2016-06-24" @default.
- W1551639504 creator A5042702595 @default.
- W1551639504 creator A5044966647 @default.
- W1551639504 creator A5052675055 @default.
- W1551639504 creator A5055137572 @default.
- W1551639504 creator A5055493437 @default.
- W1551639504 creator A5055598660 @default.
- W1551639504 creator A5068171323 @default.
- W1551639504 date "2006-04-15" @default.
- W1551639504 modified "2023-09-27" @default.
- W1551639504 title "Unwound nature of MAR-capable AT-rich DNA domains (AT-islands) targeted by a highly AT-specific drug bizelesin" @default.
- W1551639504 hasPublicationYear "2006" @default.
- W1551639504 type Work @default.
- W1551639504 sameAs 1551639504 @default.
- W1551639504 citedByCount "0" @default.
- W1551639504 crossrefType "journal-article" @default.
- W1551639504 hasAuthorship W1551639504A5042702595 @default.
- W1551639504 hasAuthorship W1551639504A5044966647 @default.
- W1551639504 hasAuthorship W1551639504A5052675055 @default.
- W1551639504 hasAuthorship W1551639504A5055137572 @default.
- W1551639504 hasAuthorship W1551639504A5055493437 @default.
- W1551639504 hasAuthorship W1551639504A5055598660 @default.
- W1551639504 hasAuthorship W1551639504A5068171323 @default.
- W1551639504 hasConcept C103244968 @default.
- W1551639504 hasConcept C104317684 @default.
- W1551639504 hasConcept C12554922 @default.
- W1551639504 hasConcept C141231307 @default.
- W1551639504 hasConcept C153911025 @default.
- W1551639504 hasConcept C185592680 @default.
- W1551639504 hasConcept C22744801 @default.
- W1551639504 hasConcept C54355233 @default.
- W1551639504 hasConcept C552990157 @default.
- W1551639504 hasConcept C86803240 @default.
- W1551639504 hasConceptScore W1551639504C103244968 @default.
- W1551639504 hasConceptScore W1551639504C104317684 @default.
- W1551639504 hasConceptScore W1551639504C12554922 @default.
- W1551639504 hasConceptScore W1551639504C141231307 @default.
- W1551639504 hasConceptScore W1551639504C153911025 @default.
- W1551639504 hasConceptScore W1551639504C185592680 @default.
- W1551639504 hasConceptScore W1551639504C22744801 @default.
- W1551639504 hasConceptScore W1551639504C54355233 @default.
- W1551639504 hasConceptScore W1551639504C552990157 @default.
- W1551639504 hasConceptScore W1551639504C86803240 @default.
- W1551639504 hasOpenAccess W1551639504 @default.
- W1551639504 hasRelatedWork W1523969484 @default.
- W1551639504 hasRelatedWork W1966136688 @default.
- W1551639504 hasRelatedWork W1968998179 @default.
- W1551639504 hasRelatedWork W1977308240 @default.
- W1551639504 hasRelatedWork W1977812228 @default.
- W1551639504 hasRelatedWork W1995861357 @default.
- W1551639504 hasRelatedWork W1998807582 @default.
- W1551639504 hasRelatedWork W2003901808 @default.
- W1551639504 hasRelatedWork W2015273793 @default.
- W1551639504 hasRelatedWork W2017588515 @default.
- W1551639504 hasRelatedWork W2019628450 @default.
- W1551639504 hasRelatedWork W2034246175 @default.
- W1551639504 hasRelatedWork W2047122757 @default.
- W1551639504 hasRelatedWork W2051299328 @default.
- W1551639504 hasRelatedWork W2065885754 @default.
- W1551639504 hasRelatedWork W2074122269 @default.
- W1551639504 hasRelatedWork W2094561276 @default.
- W1551639504 hasRelatedWork W2098501428 @default.
- W1551639504 hasRelatedWork W2107653353 @default.
- W1551639504 hasRelatedWork W2127779731 @default.
- W1551639504 hasVolume "66" @default.
- W1551639504 isParatext "false" @default.
- W1551639504 isRetracted "false" @default.
- W1551639504 magId "1551639504" @default.
- W1551639504 workType "article" @default.