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 one double-stranded RNA effector molecule or complex, comprising: (1) a sequence of at least 19 consecutive nucleotides having at least 90% identity with a nucleotide sequence within Conserved Region 1 (SEQ ID NO: 2), Conserved Region 2 (SEQ ID NO: 3), or Conserved Region 5 (SEQ ID NO: 4); active target region (ATR)-I (SEQ ID NO: 86), ATR-2 (SEQ ID NO: 87), ATR-3 (SEQ ID NO: 88), or ATR-4 (SEQ ID NO: 89); and (2) its complementary sequence.
2 . An agent for silencing hepatitis C Virus (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: 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
3 . The agent of claim 2 , wherein the double-stranded RNA effector molecules or complexes contain a double-stranded region of from 19 to 30 base pairs.
4 . The agent of claim 3 , wherein the sequence of at least 19 nucleotides and its complementary sequence are connected via a loop sequence.
5 . The agent of claim 1 , wherein at least one double-stranded RNA effector molecule has a sequence selected from SEQ ID NOs: 50, 58, 61, 71 and 72.
6 . The agent of claim 5 , wherein the expression construct contains at least two expression cassettes, each expression cassette directing the expression of at least one double-stranded RNA effector molecule.
7 . A construct for silencing a hepatitis C virus (HCV) RNA, the construct encoding at least four double-stranded RNA effector molecules or complexes wherein the construct comprises: (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: 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.
8 . The construct of claim 7 , wherein the double-stranded RNA effector molecules contain a double-stranded region of from 19 to 30 base pairs.
9 . The construct of claim 8 , wherein the sequence of at least 19 nucleotides and its complementary sequence are connected via a loop sequence.
10 . The construct of claim 7 , wherein at least one double-stranded RNA effector molecule has a sequence selected from SEQ ID NOs: 50, 58, 61, 71 and 72.
11 . The construct of claim 7 , wherein the expression construct contains at least two expression cassettes, each expression cassette directing the expression of at least one double-stranded RNA effector molecule.