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Stable triple helices are formed upon binding of RNA oligonucleotides and their 2'-O-methyl derivatives to double-helical DNA.

Authors :
Escudé C
Sun JS
Rougée M
Garestier T
Hélène C
Source :
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie [C R Acad Sci III] 1992; Vol. 315 (13), pp. 521-5.
Publication Year :
1992

Abstract

Pyrimidine oligoribonucleotides bind to the major groove of double-helical DNA at homopurine.homopyrimidine sequences. They recognize Watson-Crick base pairs by forming T.A x U and C.G x C base triplets via Hoogsteen hydrogen bonding. The stability of these triple helices is much higher than that of triple helices formed by oligodeoxyribonucleotides as shown by an increase of the temperature at which half-dissociation of the third strand occurs. When the 2'-hydroxyl group of ribose moieties is replaced by 2'-O-methyl substituent, triple helix stability is further increased.

Details

Language :
English
ISSN :
0764-4469
Volume :
315
Issue :
13
Database :
MEDLINE
Journal :
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie
Publication Type :
Academic Journal
Accession number :
1300234