INTERACTION OF DERIVATIVES OF SHORT OLIGONUCLEOTIDES WITH NUCLEIC-ACIDS .2. A TANDEM OF SHORT OLIGONUCLEOTIDES AS A HIGHLY SENSITIVE SYSTEMFOR IDENTIFICATION OF SINGLE-BASE SUBSTITUTIONS IN TARGET DNAS

Citation
Dv. Pyshnyi et al., INTERACTION OF DERIVATIVES OF SHORT OLIGONUCLEOTIDES WITH NUCLEIC-ACIDS .2. A TANDEM OF SHORT OLIGONUCLEOTIDES AS A HIGHLY SENSITIVE SYSTEMFOR IDENTIFICATION OF SINGLE-BASE SUBSTITUTIONS IN TARGET DNAS, Bioorganiceskaa himia, 23(7), 1997, pp. 561-568
Citations number
24
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
01323423
Volume
23
Issue
7
Year of publication
1997
Pages
561 - 568
Database
ISI
SICI code
0132-3423(1997)23:7<561:IODOSO>2.0.ZU;2-S
Abstract
A new approach for modification of target DNAs with tandems of derivat ives of short oligonucleotides was suggested that allows highly select ive modification of perfect duplexes only. At physiological temperatur es, the efficiency of DNA modification by a dodecanucleotide alkylatin g agent was demonstrated to be the same for both perfect and mismatch- containing duplexes, whereas the tetranucleotide reagent in the presen ce of two flanking effecters alkylated with high selectivity the targe t DNA in the perfect duplex only.