Sequence-specific cleavage of double helical DNA by triple helix formation
Homopyrimidine oligodeoxyribonucleotides with EDTA x Fe attached at a single position bind the corresponding homopyrimidine-homopurine tracts within large double-stranded DNA by triple helix formation and cleave at that site. Oligonucleotides with EDTA x Fe at the 5' end cause a sequence specific double strand break. The location and asymmetry of the cleavage pattern reveal that the homopyrimidine-EDTA probes bind in the major groove parallel to the homopurine strand of Watson-Crick double helical DNA. The sequence-specific recognition of double helical DNA by homopyrimidine probes is sensitive to single base mismatches. Homopyrimidine probes equipped with DNA cleaving moieties could be useful tools for mapping chromosomes.
- Research Organization:
- California Institute of Technology, Pasadena (USA)
- OSTI ID:
- 6806917
- Journal Information:
- Science (Washington, D.C.); (United States), Vol. 238
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
DNA
CLEAVAGE
HELICAL CONFIGURATION
PYRIMIDINES
BIOCHEMICAL REACTION KINETICS
DNA MISMATCH
DNA SEQUENCING
EDTA
GENETIC MAPPING
IRON
STRAND BREAKS
AMINO ACIDS
AZINES
CARBOXYLIC ACIDS
CHELATING AGENTS
CONFIGURATION
CRYSTAL STRUCTURE
ELEMENTS
HETEROCYCLIC COMPOUNDS
KINETICS
MAPPING
METALS
MICROSTRUCTURE
NUCLEIC ACIDS
ORGANIC ACIDS
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
REACTION KINETICS
STRUCTURAL CHEMICAL ANALYSIS
TRANSITION ELEMENTS
500200* - Environment
Atmospheric- Chemicals Monitoring & Transport- (-1989)