ID | 113344 |
Author |
Kikuchi, Yusaku
The University of Tokushima
Yamazaki, Naoshi
The University of Tokushima
Tokushima University Educator and Researcher Directory
KAKEN Search Researchers
Tarashima, Noriko
The University of Tokushima
Tokushima University Educator and Researcher Directory
KAKEN Search Researchers
Takiguchi, Yoshiharu
The University of Tokushima
Tokushima University Educator and Researcher Directory
KAKEN Search Researchers
Itoh, Kohji
The University of Tokushima
Tokushima University Educator and Researcher Directory
KAKEN Search Researchers
Minakawa, Noriaki
The University of Tokushima
Tokushima University Educator and Researcher Directory
KAKEN Search Researchers
|
Keywords | Oligonucleotide
2'-Modified-4'-thioRNA
Gene suppression
U1 snRNA interference
|
Content Type |
Journal Article
|
Description | Gene suppression via U1 small nuclear RNA interference (U1i) is considered to be one of the most attractive approaches, and takes the place of general antisense, RNA interference (RNAi), and anti-micro RNA machineries. Since the U1i can be induced by short oligonucleotides (ONs), namely U1 adaptors consisting of a ‘target domain’ and a ‘U1 domain’, we prepared adaptor ONs using 2'-modified-4'-thionucleosides developed by our group, and evaluated their U1i activity. As a result, the desired gene suppression via U1i was observed in ONs prepared as a combination of 2'-fluoro-4'-thionucleoside and 2'-fluoronucleoside units as well as only 2'-fluoronucleoside units, while those prepared as combination of 2'-OMe nucleoside/2'-OMe-4'-thionucleoside and 2'-fluoronucleoside units did not show significant activity. Measurement of Tm values indicated that a higher hybridization ability of adaptor ONs with complementary RNA is one of the important factors to show potent U1i activity.
|
Journal Title |
Bioorganic & Medicinal Chemistry
|
ISSN | 09680896
|
NCID | AA10938083
AA11522681
|
Publisher | Elsevier
|
Volume | 21
|
Issue | 17
|
Start Page | 5292
|
End Page | 5296
|
Published Date | 2013-06-18
|
Rights | ©2013 The Authors. Published by Elsevier Ltd.Open access under CC BY-NC-ND license.(https://creativecommons.org/licenses/by-nc-nd/3.0/)
|
EDB ID | |
DOI (Published Version) | |
URL ( Publisher's Version ) | |
FullText File | |
language |
eng
|
TextVersion |
Publisher
|
departments |
Pharmaceutical Sciences
|