Transgene cassettes, AAV vectors and AAV viral vectors for the expression of human codon-optimized SLC6A1
The present disclosure provides methods and compositions for the treatment of diseases and genetic disorders linked to SLC6A1 loss and/or misfunction. The methods and compositions of the present disclosure comprise rAAV vectors and rAAV viral vectors comprising transgene nucleic acid molecules comprising nucleic acid sequences encoding for a GAT1 polypeptide.
1. A recombinant adeno-associated virus (rAAV) vector comprising in 5′ to 3′ direction:
(a) a first AAV inverted terminal repeat (ITR) sequence;
(b) a promoter sequence;
(c) a transgene nucleic acid molecule of SEQ ID NO: 3 or SEQ ID NO: 6
(d) a polyA sequence; and
(e) a second AAV ITR sequence.
2. The rAAV vector of claim 1 , wherein the first AAV ITR sequence comprises the nucleic acid sequence set forth in SEQ ID NO: 12.
3. The rAAV vector of claim 1 , wherein the second AAV ITR sequence comprises the nucleic acid sequence set forth in SEQ ID NO: 13.
4. The rAAV vector of claim 1 , wherein the promoter sequence comprises a Rous sarcoma virus (RSV) LTR promoter (optionally with the RSV enhancer), a cytomegalovirus (CMV) promoter, an SV40 promoter, a dihydrofolate reductase promoter, a beta-actin promoter, a phosphoglycerol kinase (PGK) promoter, a U6 promoter, an H1 promoter, a CAG promoter, a hybrid chicken beta-actin promoter, an MeCP2 promoter, an EF1 promoter, a ubiquitous chicken β-actin hybrid (CBh) promoter, a U1a promoter, a U1b promoter, an MeCP2 promoter, an MeP418 promoter, an MeP426 promoter, a minimal MeCP2 promoter, a VMD2 promoter, an mRho promoter, EFla promoter, Ubc promoter, human β-actin promoter, TRE promoter, Ac5 promoter, Polyhedrin promoter, CaMKIIa promoter, Gal1 promoter, TEF1 promoter, GDS promoter, ADH1 promoter, Ubi promoter, or α-1-antitrypsin (hAAT) promoter.
5. The rAAV vector of claim 1 , wherein the promoter sequence comprises the nucleic acid sequence set forth in SEQ ID NO: 14.
6. The rAAV vector of claim 1 , wherein the promoter sequence comprises the nucleic acid sequence set forth in SEQ ID NO: 15.
7. The rAAV vector of claim 1 , wherein the polyA sequence comprises the nucleic acid sequence set forth in SEQ ID NO: 16.
8. The rAAV vector of claim 1 , comprising, in the 5′ to 3′ direction:
a) a first AAV ITR sequence comprising the nucleic acid sequence set forth in SEQ ID NO: 12;
b) a promoter sequence comprising the nucleic acid sequence set forth in SEQ ID NO: 14;
c) a transgene nucleic acid molecule, wherein the transgene nucleic acid molecule comprises a nucleic acid sequence encoding for a GAT1 polypeptide, wherein the nucleic acid sequence encoding for a GAT1 polypeptide comprises the nucleic acid sequence set forth in SEQ ID NO: 3;
d) a polyA sequence comprising the nucleic acid sequence set forth in SEQ ID NO: 16; and
e) a second AAV ITR sequence comprising the nucleic acid sequence set forth in SEQ ID NO: 13.
9. The rAAV vector of claim 1 , comprising, in the 5′ to 3′ direction:
a) a first AAV ITR sequence comprising the nucleic acid sequence set forth in SEQ ID NO: 12;
b) a promoter sequence comprising the nucleic acid sequence set forth in SEQ ID NO: 15;
c) a transgene nucleic acid molecule, wherein the transgene nucleic acid molecule comprises a nucleic acid sequence encoding for a GAT1 polypeptide, wherein the nucleic acid sequence encoding for a GAT1 polypeptide comprises the nucleic acid sequence set forth in SEQ ID NO: 3;
d) a polyA sequence comprising the nucleic acid sequence set forth in SEQ ID NO: 16; and
e) a second AAV ITR sequence comprising the nucleic acid sequence set forth in SEQ ID NO: 13.
10. The rAAV vector of claim 1 , wherein the rAAV vector comprises the nucleic acid sequence set forth in SEQ ID NO: 20.
11. The rAAV vector of claim 1 , wherein the rAAV vector comprises the nucleic acid sequence set forth in SEQ ID NO: 22.
12. An rAAV viral vector comprising
(i) an AAV capsid protein; and
(ii) an rAAV vector of claim 1 .
13. The rAAV viral vector of claim 12 , wherein the AAV capsid protein is an AAV1 capsid protein, an AAV2 capsid protein, an AAV4 capsid protein, an AAV5 capsid protein, an AAV6 capsid protein, an AAV7 capsid protein, an AAV8 capsid protein, an AAV9 capsid protein, an AAV10 capsid protein, an AAV11 capsid protein, an AAV12 capsid protein, an AAV13 capsid protein, an AAVPHP.B capsid protein, an AAVrh74 capsid protein or an AAVrh.10 capsid protein.
14. The rAAV viral vector of claim 12 , wherein the AAV capsid protein is an AAV9 capsid protein.
15. A pharmaceutical composition comprising:
a) the rAAV viral vector of claim 12 ; and at least one pharmaceutically acceptable excipient and/or additive.
16. A method for treating a subject having a disease and/or disorder involving a SLC6A1 gene, the method comprising administering to the subject at least one therapeutically effective amount of the rAAV viral vector of claim 12 .
17. The method of claim 16 , wherein the disease and/or disorder involving the SLC6A1 gene is SLC6A1 haploinsufficiency or Doose Syndrome.
18. The method of claim 16 , wherein the rAAV viral vector is administered to the subject at a dose ranging from about 10 11 to about 10 18 viral vector particles.
19. The method of claim 18 , wherein the rAAV viral vector is administered to the subject at a dose ranging from about 10 13 to about 10 16 viral vector particles.
20. The method of claim 16 , wherein the rAAV viral vector is administered to the subject intravenously, intrathecally, intracerebrally, intraventricularly, intranasally, intratracheally, intra-aurally, intra-ocularly, or peri-ocularly, orally, rectally, transmucosally, inhalationally, transdermally, parenterally, subcutaneously, intradermally, intramuscularly, intracisternally, intranervally, intrapleurally, topically, intralymphatically, intracisternally or intranerve.
21. The method of claim 20 , wherein the rAAV viral vector is administered intrathecally.