Hepatitis C dsRNA effector molecules, expression constructs, compositions, and methods of use
The present invention provides agents, compositions, constructs and methods for silencing HCV polynucleotides, as well as methods and compositions for treating or preventing HCV infection in a mammalian cell. In one aspect, the present invention provides an agent or composition comprising at least one double-stranded RNA effector molecule or complex. The double-stranded RNA effector molecule or complex comprises: (1) a sequence of at least 19 nucleotides having at least 90% identity with a nucleotide sequence within HCV Conserved Region 1 (SEQ ID NO: 2), HCV Conserved Region 2 (SEQ ID NO: 3), HCV Conserved Region 5 (SEQ ID NO: 4), (ATR)-1 (SEQ ID NO: 86), ATR-2 (SEQ ID NO: 87), ATR-3 (SEQ ID NO: 88), ATR-4 (SEQ ID NO: 89); and (2) its complementary sequence. In another aspect, the present invention provides a construct suitable for replication in a host cell, and/or suitable for expression of an RNA molecule or complex of the invention in vitro or in vivo. In a third aspect, the present invention provides a method for silencing HCV RNA in a mammalian cell, which comprises administering to the mammalian cell an agent, composition, or construct of the invention in a manner and amount effective to silence HCV RNA in the cell. In a related aspect, the invention provides a method for treating or preventing HCV infection in a patient, comprising administering to the patient an effective amount of an agent, composition, or construct of the invention as described herein.
1. A method for silencing an hepatitis C virus (HCV) RNA in a mammalian cell comprising administering to said cell at least four double-stranded RNA effector molecules or complexes, comprising: (a) (1) a sequences of at least 19 consecutive nucleotides having at least 90% identity with a nucleotide sequence of SEQ ID NO: 19, SEQ ID NO: 32, SEQ ID NO: 22, and SEQ ID NO: 33; and (2) their complementary sequences; or (b) (1) sequences of at least 19 nucleotides having at least 90% identity with a nucleotide sequence of SEQ ID NO: 19, SEQ ID NO: 11, SEQ ID NO: 22, and SEQ ID NO: 33; and (2) their complementary sequences.
2. The method of claim 1 , wherein the double-stranded RNA effector molecules or complexes comprise a double-stranded region of from 19 to 30 base pairs.
3. The method of claim 2 , wherein the sequence of at least 19 nucleotides and its complementary sequence are connected via a loop sequence.
4. The method of claim 1 , wherein said administering is accomplished by providing to the mammalian cell at least one expression construct capable of expressing the double-stranded RNA effector molecule(s).
5. The method of claim 1 , wherein the mammalian cell is a human cell.
6. A method of treating hepatitis C virus (HCV) infection in a patient, comprising administering to said patient an effective amount of an agent for silencing HCV RNA, comprising at least four double stranded RNA effector molecules or complexes that comprise, or a construct that expresses: (a) (1) sequences of at least 19 nucleotides having at least 90% identity with a nucleotide sequence of SEQ ID NO: 19, SEQ ID NO: 31, SEQ ID NO: 22, and SEQ ID NO: 33; and (2) their complementary sequences; or (b) (1) sequences of at least 19 nucleotides having at least 90% identity with a nucleotide sequence of SEQ ID NO: 19, SEQ ID NO: 11, SEQ ID NO: 22, and SEQ ID NO: 33; and (2) their complementary sequences.
7. The method of claim 6 , wherein at least one double-stranded RNA effector molecule has a sequence selected from SEQ ID NOs: 50, 58, 61, 71, and 72.