Conserved HBV and HCV sequences useful for gene silencing
View Patent ↗Conserved consensus sequences from known hepatitis B virus strains and known hepatitis C virus strains, which are useful in inhibiting the expression of the viruses in mammalian cells, are provided. These sequences are useful to silence the genes of HBV and HCV, thereby providing therapeutic utility against HBV and HCV viral infection in humans.
1. A method for inhibiting expression of a polynucleotide sequence of hepatitis B virus in an in vivo mammalian cell comprising administering to said cell a double-stranded RNA effector molecule comprising an at least 19 contiguous base pair nucleotide sequence in a double-stranded conformation, wherein said double-stranded RNA effector molecule comprises a sequence selected from the group consisting of SEQ ID NOs 18-22 where U is substituted for T.
2. A method for inhibiting expression of a polynucleotide sequence of hepatitis B virus in an in vivo mammalian cell comprising administering to said cell a double-stranded RNA effector molecule comprising an at least 19 contiguous base pair nucleotide sequence in a double-stranded conformation wherein said double-stranded RNA effector molecule comprises a sequence selected from the group consisting of SEQ ID NOs 18-22 where U is substituted for T and wherein expression of said double-stranded RNA effector molecule in an HBV cell culture transfection assay mediates at least 87% inhibition of HBsAg level relative to control lacking said effector molecule.
3. A composition for inhibiting the expression of a polynucleotide sequence of hepatitis B virus in an in vivo mammalian cell comprising a double-stranded RNA effector molecule, comprising an at least 19 contiguous base pair nucleotide sequence in a double-stranded conformation, wherein said double-stranded RNA effector molecule comprises a sequence selected from the group consisting of SEQ ID NOs 18-22 where U is substituted for T.
4. A composition for inhibiting the expression of a polynucleotide sequence of hepatitis B virus in an in vivo mammalian cell comprising a double-stranded RNA effector molecule, comprising an at least 19 contiguous base pair nucleotide sequence in a double-stranded conformation, wherein said double-stranded RNA effector molecule comprises a sequence selected from the group consisting of SEQ ID NOs 18-22 where U is substituted for T and wherein expression of said double-stranded RNA effector molecule in an HBV cell culture transfection assay mediates at least 87% inhibition of HBsAg level relative to control lacking said effector molecule.