Agent for suppressing expression of dominant allele
AssigneeLsip, LLC
InventorsHirohiko Hohjoh, Masaki Takahashi
Life of this patent
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Abstract
An agent for selectively suppressing the expression of a dominant allele while allowing expression of wild-type or desired alleles and methods for using the agent are described. The RNAi agent has a structure obtained by assigning a dominant point mutation in the targeted allele as a standard point, setting a base length from the standard point to the 5′ end to a predetermined length, and introducing one mismatch base differing from the target sequence to a predetermined position downstream from the standard point.
Claims9
An agent for suppressing expression of a dominant allele of a target gene comprising an RNAi molecule, wherein the RNAi molecule comprises
- an RNAi sense strand region consisting of a nucleotide sequence identical to any one 16-base to 30-base consecutive nucleotide sequence in the sense strand of the dominant allele comprising at least one dominant point mutation and an RNAi antisense strand region consisting of a nucleotide sequence complementary thereto, wherein:
- any one base at the 7th to 10th positions upstream from any one dominant point mutation in the RNAi sense strand region constitutes the 5′-terminal base of the sense strand of the RNAi molecule;
- and
- any one base at the 3rd to 8th positions downstream from the any one dominant point mutation is a mismatch base different from the corresponding base in the nucleotide sequence in the sense strand of the dominant allele,
- wherein the dominant point mutation is involved in the onset of a non-small cell lung cancer, the target gene is epidermal growth factor receptor (EGFR) gene, and
- the sense and antisense strands of the RNAi molecule consist of an oligonucleotide pair shown in SEQ ID NOs;
- 81 and 82 or SEQ ID NOs:
- 83 and 84, respectively.
An agent for suppressing expression of a dominant allele of a target gene comprising an RNAi molecule, wherein the RNAi molecule comprises
- an RNAi sense strand region consisting of a nucleotide sequence identical to any one 16-base to 30-base consecutive nucleotide sequence in the sense strand of the dominant allele comprising at least one dominant point mutation and an RNAi antisense strand region consisting of a nucleotide sequence complementary thereto, wherein:
- any one base at the 7th to 10th positions upstream from any one dominant point mutation in the RNAi sense strand region constitutes the 5′-terminal base of the sense strand of the RNAi molecule;
- and
- any one base at the 3rd to 8th positions downstream from the any one dominant point mutation is a mismatch base different from the corresponding base in the nucleotide sequence in the sense strand of the dominant allele,
- wherein the dominant point mutation is involved in the onset of fibrodysplasia ossificans progressiva, the target gene is activin-like kinase 2 (ALK2) gene, and the sense and antisense strands of the RNAi molecule are selected from the group consisting of oligonucleotide pairs shown in SEQ ID NOs:
- 3 and 4, SEQ ID NOs:
- 5 and 6, SEQ ID NOs:
- 7 and 8, SEQ ID NOs:
- 9 and 10, SEQ ID NOs:
- 11 and 12, SEQ ID NOs:
- 13 and 14, SEQ ID NOs:
- 19 and 20, SEQ ID NOs:
- 21 and 22, SEQ ID NOs:
- 23 and 24, SEQ ID NOs:
- 25 and 26, SEQ ID NOs:
- 27 and 28, SEQ ID NOs:
- 29 and 30, SEQ ID NOs:
- 35 and 36, SEQ ID NOs:
- 37 and 38, SEQ ID NOs:
- 39 and 40, SEQ ID NOs:
- 41 and 42, SEQ ID NOs:
- 43 and 44, and SEQ ID NOs:
- 91 and 92, respectively.
An agent for suppressing expression of a dominant allele of a target gene comprising an RNAi molecule, wherein the RNAi molecule comprises
- an RNAi sense strand region consisting of a nucleotide sequence identical to any one 16-base to 30-base consecutive nucleotide sequence in the sense strand of the dominant allele comprising at least one dominant point mutation and an RNAi antisense strand region consisting of a nucleotide sequence complementary thereto, wherein:
- any one base at the 7th to 10th positions upstream from any one dominant point mutation in the RNAi sense strand region constitutes the 5′-terminal base of the sense strand of the RNAi molecule;
- and
- any one base at the 3rd to 8th positions downstream from the any one dominant point mutation is a mismatch base different from the corresponding base in the nucleotide sequence in the sense strand of the dominant allele,
- wherein the dominant point mutation is involved in the onset of Huntington's disease, the target gene is huntingtin gene, and the sense and antisense strands of the RNAi molecule are selected from the group consisting of oligonucleotide pairs shown in SEQ ID NOs:
- 55 and 56, SEQ ID NOs:
- 57 and 58, SEQ ID NOs:
- 59 and 60, SEQ ID NOs:
- 61 and 62, SEQ ID NOs:
- 63 and 64, SEQ ID NOs:
- 67 and 68, and SEQ ID NOs:
- 69 and 70, respectively.
Dependencies are inferred from the claim text.