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PMID: 1300234 Published · ppublish English Journal Article

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

Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie ·Vol. 315 ·No. 13 ·1992-00-00 ·Pages 521-5

Escudé C, Sun JS, Rougée M, Garestier T, Hélène C

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.

MeSH Terms
Biophysical Phenomena Biophysics DNA, Superhelical/chemical synthesis,metabolism Drug Stability In Vitro Techniques Nucleic Acid Conformation Oligoribonucleotides/metabolism
Chemicals
DNA, Superhelical Oligoribonucleotides
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Escudé C
Laboratoire de Biophysique, INSERM U n. 201-CNRS-URA n. 481, Paris.
Sun J S
Rougée M
Garestier T
Hélène C
Article Info
Journal
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie
Abbr.
C R Acad Sci III
ISSN
0764-4469
Published
1992-00-00
Pages
521-5
Language
English
Region
France
NLM ID
8503078
Subset
IM
External Links
PubMed source
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