Engineered Guide RNAs and Polynucleotides
Disclosed herein are engineered guide RNAs and compositions comprising the same for treatment of diseases or conditions in a subject. Also disclosed herein are methods of treating diseases or conditions in a subject by administering engineered guide RNAs or pharmaceutical compositions described herein.
1 . A composition comprising an engineered guide RNA or a polynucleotide encoding the engineered guide RNA, wherein the engineered guide RNA has complementarity to a target sequence of a target SNCA RNA and comprises a polynucleotide sequence having at least 80% sequence identity to any one of SEQ ID NOS: 2-285, SEQ ID NOS: 293-299, SEQ ID NOS: 333-357, SEQ ID NOS: 375-376, SEQ ID NOS: 380-381, SEQ ID NOS: 390-440, or SEQ ID NOS: 777-784.
2 . (canceled)
3 . (canceled)
4 . The composition of claim 1 , wherein the target sequence of the target SNCA RNA comprises a translation initiation site.
5 . The composition of claim 4 , wherein the translation initiation site is the SNCA Codon 1 translation initiation site of Exon 2.
6 . The composition of claim 5 , wherein the translation initiation site is the SNCA Codon 1 translation initiation site of Exon 2 corresponding to position 226 of an SNCA transcript variant 1 of accession number NM_000345.4.
7 . The composition of claim 1 , wherein upon hybridization of the engineered guide RNA to the target sequence of the target SNCA RNA, a guide-target RNA scaffold is formed that has one or more structural features that is not present within the engineered guide RNA prior to the hybridization, and wherein the one or more structural features comprises at least a first 6/6 symmetric internal loop and at least a second 6/6 symmetric loop.
8 . The composition of claim 7 , wherein the first 6/6 symmetric internal loop is at a position selected from the group consisting of: 33, 32, 30, 28, and 26; relative to a target adenosine at position 0.
9 . The composition of claim 8 , wherein the first 6/6 symmetric internal loop is at position 33, relative to the target adenosine at position 0.
10 . (canceled)
11 . The composition of claim 9 , wherein the engineered guide RNA comprises at least 80% sequence identity to an one of SEQ ID NO: 337, SEQ ID NO: 338, SEQ ID NO: 339, SEQ ID NO: 340, SEQ ID NO: 298, SEQ ID NO: 299, or SEQ ID NO: 299.
12 .- 19 . (canceled)
20 . The composition of claim 8 , wherein the first 6/6 symmetric internal loop is at position 32, relative to the target adenosine at position 0.
21 . (canceled)
22 . The composition of claim 20 , wherein the engineered guide RNA comprises at least 80% sequence identity to an one of SEQ ID NO: 333, SEQ ID NO: 334, SEQ ID NO: 335, SEQ ID NO: 336, or SEQ ID NO: 295.
23 .- 30 . (canceled)
31 . The composition of claim 8 , wherein the first 6/6 symmetric internal loop is at position 30, relative to the target adenosine at position 0.
32 . (canceled)
33 . The composition of claim 31 , wherein the engineered guide RNA comprises at least 80% sequence identity to SEQ ID NO: 297.
34 . The composition of claim 8 , wherein the first 6/6 symmetric internal loop is at position 28, relative to the target adenosine at position 0.
35 . (canceled)
36 . The composition of claim 34 , wherein the engineered guide RNA comprises at least 80% sequence identity to SEQ ID NO: 293 or SEQ ID NO: 294.
37 . (canceled)
38 . (canceled)
39 . The composition of claim 8 , wherein the first 6/6 symmetric internal loop is at position 26, relative to the target adenosine at position 0.
40 . (canceled)
41 . The composition of claim 39 , wherein the engineered guide RNA comprises at least 80% sequence identity to SEQ ID NO: 296.
42 .- 47 . (canceled)
48 . The composition of claim 1 , wherein upon hybridization of the engineered guide RNA to the target sequence of the target SNCA RNA, the engineered guide RNA facilitates RNA editing of one or more adenosines in the target sequence of the target SNCA RNA by an ADAR enzyme.
49 . (canceled)
50 . (canceled)
51 . (canceled)
52 . The composition of claim 51 , wherein the engineered guide RNA is encoded by a viral vector.
53 . The composition of claim 52 , wherein the viral vector is an adeno-associated viral (AAV) vector.
54 . The composition of claim 53 , wherein the AAV vector is an AAV1 vector, AAV2 vector, AAV3 vector, AAV4 vector, AAV5 vector, AAV6 vector, AAV7 vector, AAV8 vector, AAV9 vector, AAV10 vector, AAV 11 vector, or a derivative, a chimera, or a variant of any of these.
55 .- 83 . (canceled)
84 . A method of treating a Parkinson's disease in a subject in need thereof, the method comprising: administering to the subject a composition that comprises an engineered guide RNA or a polynucleotide encoding the engineered guide RNA, wherein the engineered guide RNA has complementarity to a target sequence of a target SNCA RNA and comprises a polynucleotide sequence having at least 80% sequence identity to any one of SEQ ID NOS: 2-285, SEQ ID NOS: 293-299, SEQ ID NOS: 333-357, SEQ ID NOS: 375-376, SEQ ID NOS: 380-381, SEQ ID NOS: 390-440, or SEQ ID NOS: 777-784, wherein the administering results in treatment of the Parkinson's disease in the subject.
85 . The method of claim 84 , wherein the treating comprises reducing one or more symptoms of the Parkinson's disease in the subject selected from the group consisting of muscle tone rigidity, bradykinesia, resting tremor, and any combination thereof, relative to prior to the administering.
86 .- 117 . (canceled)
118 . The composition of claim 1 , wherein hybridization of the engineered guide RNA to the target sequence of the target SNCA RNA results in knockdown of alpha-synuclein protein encoded by the target SNCA RNA.