Effect of base modifications on structure, thermodynamic stability, and gene silencing activity of short interfering RNA

• Published in: RNA (Cambridge) 2007-08, Vol.13 (8), p.1301-1316
• Main Authors: Sipa, Katarzyna, Sochacka, Elzbieta, Kazmierczak-Baranska, Julia, Maszewska, Maria, Janicka, Magdalena, Nowak, Genowefa, Nawrot, Barbara
• Format: Article
• Language: English
• Subjects: Circular Dichroism; Green Fluorescent Proteins - metabolism; HeLa Cells; Humans; Nucleic Acid Conformation; Nucleosides - chemistry; RNA Interference; RNA, Double-Stranded - metabolism; RNA, Small Interfering - chemistry; RNA, Small Interfering - metabolism; Thermodynamics; Uridine - analogs & derivatives; Uridine - metabolism
• ISSN: 1355-8382; 1469-9001
• DOI: 10.1261/rna.538907

A series of nucleobase-modified siRNA duplexes containing "rare" nucleosides, 2-thiouridine (s(2)U), pseudouridine (Psi), and dihydrouridine (D), were evaluated for their thermodynamic stability and gene silencing activity. The duplexes with modified units at terminal positions exhibited similar stability as the nonmodified reference. Introduction of the s(2)U or Psi units into the central part of the antisense strand resulted in duplexes with higher melting temperatures (Tm). In contrary, D unit similarly like wobble base pair led to the less stable duplexes (DeltaTm 3.9 and 6.6 degrees C, respectively). Gene-silencing activity of siRNA duplexes directed toward enhanced green fluorescent protein or beta-site APP cleaving enzyme was tested in a dual fluorescence assay. The duplexes with s(2)U and Psi units at their 3'-ends and with a D unit at their 5'-ends (with respect to the guide strands) were the most potent gene expression inhibitors. Duplexes with s(2)U and Psi units at their 5'-ends were by 50% less active than the nonmodified counterpart. Those containing a D unit or wobble base pair in the central domain had the lowest Tm, disturbed the A-type helical structure, and had more than three times lower activity than their nonmodified congener. Activity of siRNA containing the wobble base pair could be rescued by placing the thio-nucleoside at the position 3'-adjacent to the mutation site. Thermally stable siRNA molecules containing several s(2)U units in the antisense strand were biologically as potent as their native counterparts. The present results provide a new chemical tool for modulation of siRNA gene-silencing activity.