| Literature DB >> 8785472 |
C Leydier1, L Bellon, J L Barascut, F Morvan, B Rayner, J L Imbach.
Abstract
4'-Thio-beta-D-oligoribonucleotides (12 mer and 16 mer) containing a mixed base sequence were synthesized via the phosphoramidite solid support approach. These RNA analogs showed very good nuclease resistance as compared with wild-type RNA. Furthermore, 4'-thio-beta-D-oligoribonucleotides were shown to hybridize with a complementary DNA or RNA strand to form a duplex or with a DNA hairpin to form a triple helix. 4'-Thio-RNA binds more tightly to its complementary RNA strand than to its complementary DNA strand. A 4'-thio-RNA:RNA duplex is as stable as a 2'-O-methyl-RNA:RNA duplex. 4'-Thio-RNA, however, forms a 4'-thio-RNA:DNA:DNA triplex with a stability similar to the corresponding triplex with all wild-type DNA.Entities:
Mesh:
Substances:
Year: 1995 PMID: 8785472 DOI: 10.1089/ard.1995.5.167
Source DB: PubMed Journal: Antisense Res Dev ISSN: 1050-5261