Preferential, cooperative binding of DNA topoisomerase II to scaffold-associated regions
about
Compartmentalization within the nucleus: discovery of a novel subnuclear regionCharacterization of SAF-A, a novel nuclear DNA binding protein from HeLa cells with high affinity for nuclear matrix/scaffold attachment DNA elementsStructure and function of type II DNA topoisomerasesThe novel SAR-binding domain of scaffold attachment factor A (SAF-A) is a target in apoptotic nuclear breakdown.Scaffold/matrix attachment region elements interact with a p300-scaffold attachment factor A complex and are bound by acetylated nucleosomes.Purification and molecular cloning of the scaffold attachment factor B (SAF-B), a novel human nuclear protein that specifically binds to S/MAR-DNALocalization of RAP1 and topoisomerase II in nuclei and meiotic chromosomes of yeast.ScII: an abundant chromosome scaffold protein is a member of a family of putative ATPases with an unusual predicted tertiary structure.An integrated Drosophila model system reveals unique properties for F14512, a novel polyamine-containing anticancer drug that targets topoisomerase IIPossible role of DNA topoisomerase II on transcription of the homeobox gene Hox-2.1 in F9 embryonal carcinoma cellsThe matrix attachment region in the Chinese hamster dihydrofolate reductase origin of replication may be required for local chromatid separation.Topoisomerase II, scaffold component, promotes chromatin compaction in vitro in a linker-histone H1-dependent mannerNuclear scaffold attachment stimulates, but is not essential for ARS activity in Saccharomyces cerevisiae: analysis of the Drosophila ftz SAREukaryotic topoisomerases recognize nucleic acid topology by preferentially interacting with DNA crossoversIn vivo topoisomerase II cleavage of the Drosophila histone and satellite III repeats: DNA sequence and structural characteristicsOn the components of segregation distortion in Drosophila melanogaster. V. Molecular analysis of the Sd locus.A model for chromatin opening: stimulation of topoisomerase II and restriction enzyme cleavage of chromatin by distamycin.SAR-dependent mobilization of histone H1 by HMG-I/Y in vitro: HMG-I/Y is enriched in H1-depleted chromatin.Kinetics of chromosome condensation in the presence of topoisomerases: a phantom chain model.Novel functional MAR elements of double minute chromosomes in human ovarian cells capable of enhancing gene expression.Maintenance of a functional higher order chromatin structure: The role of the nuclear matrix in normal and disease states.Dynamics of human DNA topoisomerases IIalpha and IIbeta in living cellsDistribution of topoisomerase II-mediated cleavage sites and relation to structural and functional landmarks in 830 kb of Drosophila DNABase sequence determinants of amonafide stimulation of topoisomerase II DNA cleavage.Synthesis of signals for de novo DNA methylation in Neurospora crassa.Different topoisomerase II antitumor drugs direct similar specific long-range fragmentation of an amplified c-MYC gene locus in living cells and in high-salt-extracted nuclei.SARs stimulate but do not confer position independent gene expression.Stimulation of Tat-independent transcriptional processivity from the HIV-1 LTR promoter by matrix attachment regions.Local sensing of global DNA topology: from crossover geometry to type II topoisomerase processivityCondensin HEAT subunits required for DNA repair, kinetochore/centromere function and ploidy maintenance in fission yeastSupragenic loop organization: mapping in Drosophila embryos, of scaffold-associated regions on a 800 kilobase DNA continuum cloned from the 14B-15B first chromosome region.Homologue pairing in flies and mammals: gene regulation when two are involved.Chromatin condensation during apoptosis is accompanied by degradation of lamin A+B, without enhanced activation of cdc2 kinase.Association of chromosome territories with the nuclear matrix. Disruption of human chromosome territories correlates with the release of a subset of nuclear matrix proteins.Developmental regulation of Drosophila DNA topoisomerase IIAn RNase-sensitive particle containing Drosophila melanogaster DNA topoisomerase II.A soluble transcription factor, Oct-1, is also found in the insoluble nuclear matrix and possesses silencing activity in its alanine-rich domain.The matrix attachment region-binding protein SATB1 participates in negative regulation of tissue-specific gene expression.Clusters of S1 nuclease-hypersensitive sites induced in vivo by DNA damageTopoisomerase II forms multimers in vitro: effects of metals, beta-glycerophosphate, and phosphorylation of its C-terminal domain.
P2860
Q22066162-662C7BB3-5C36-4763-B3D2-5B5F6C02F8A5Q24337072-FA84059A-E4FA-4BD0-AD7E-37B7194F2B7EQ24528489-C95F645D-6AA1-4F30-A86D-BEB8A692203AQ24532883-78B3CC15-406A-4CA4-8210-7C1DA7D3E558Q24537237-DFCBFC29-DA39-4923-B7AF-1520DE28A6A6Q24546105-1C1AE05E-A682-4509-9ED3-FD5372D626E4Q27932347-3F3BE750-0785-4255-B184-E6F0CABBC5BCQ27932431-749B7EE3-359E-4C18-8401-95746DD26E28Q28476505-77C46F18-B2D9-4E69-B130-4FA23259C03FQ28509477-0104A182-0DE7-42AE-8B33-32A74518CC75Q30310624-08A9034E-4F63-46D3-BFA5-92184B72645BQ30479543-11BDC731-72FD-42CB-A146-6BFF0031DB10Q33923320-BE82A82F-753C-46F9-B759-02FBA205A0D5Q33923932-DEFCA7DC-5653-4E4B-8679-70066CF1D890Q33937443-15630AC0-9068-4FA8-A7FF-06F50479DBC9Q33958274-EE3D338E-0FFC-4405-AECD-99EA85C1D2E8Q34040750-13A74FAA-60AD-4773-AD7A-720EB8F37C1EQ34057694-3368F52D-50CC-4F49-A908-28036D7EF7ABQ34115032-A7A3E7D1-885D-4672-BB85-5CD4923DC011Q34154580-52B93EED-1668-4B02-914F-F19448E67E7FQ34189725-808FD17C-BFFB-43ED-8627-BD70A7443922Q34522098-ACB8F709-FD75-4C4C-A165-6BED879BEF15Q34629963-F55E5521-8234-4EDC-B083-532B4F289DD9Q34735018-58FA23FD-761A-49C6-957E-BC3AB4EF9082Q34784740-CCCB2963-2F7F-44C5-AF51-AAB12B82F7BAQ34806472-8BAFE380-E451-475D-A552-7FCFF01E3418Q34888570-D213135D-F013-4F7F-983E-C4910453DC57Q35107931-6771830A-2B4D-42B1-A7E3-98D5C1DEABB0Q35468217-D19B6DCF-5EC7-40FF-B160-68670D8E7406Q35575780-BFA7E09C-F018-4C2A-8ECE-0720F56EC2A4Q35847656-E628FD16-182A-4DF9-AA63-B96DB226C2F1Q35910233-86A21F40-815B-40D0-B58B-2E3C3B1B2F34Q36234491-C7543C62-FADC-49FB-91B5-57AE2F70A37DQ36293303-CB2C21A0-0A8E-437F-9B2D-B387B41FC708Q36529104-6239F4C6-A4F0-49FE-ACAE-B26E99FDB85AQ36534992-741B3940-3AFE-4D10-8072-3B5641EC25F1Q36561509-DA5CE51F-62B2-4343-8F92-BF04C4364028Q36571699-1D7505D4-30B2-4151-B3E6-4A25BFDB68A9Q36572117-9BEDD8DC-8088-4BEF-BCBA-4F6EB1F7CDF7Q36668278-5A00C34D-19F4-4A89-B5EE-EB47CE97DD83
P2860
Preferential, cooperative binding of DNA topoisomerase II to scaffold-associated regions
description
1989 nî lūn-bûn
@nan
1989 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Preferential, cooperative binding of DNA topoisomerase II to scaffold-associated regions
@ast
Preferential, cooperative binding of DNA topoisomerase II to scaffold-associated regions
@en
Preferential, cooperative binding of DNA topoisomerase II to scaffold-associated regions.
@nl
type
label
Preferential, cooperative binding of DNA topoisomerase II to scaffold-associated regions
@ast
Preferential, cooperative binding of DNA topoisomerase II to scaffold-associated regions
@en
Preferential, cooperative binding of DNA topoisomerase II to scaffold-associated regions.
@nl
prefLabel
Preferential, cooperative binding of DNA topoisomerase II to scaffold-associated regions
@ast
Preferential, cooperative binding of DNA topoisomerase II to scaffold-associated regions
@en
Preferential, cooperative binding of DNA topoisomerase II to scaffold-associated regions.
@nl
P2860
P1433
P1476
Preferential, cooperative binding of DNA topoisomerase II to scaffold-associated regions
@en
P2860
P304
P407
P577
1989-12-01T00:00:00Z