Optimized factor VIII genes
The present disclosure provides codon optimized Factor VIII sequences, vectors, and host cells comprising codon optimized Factor VIII sequences, polypeptides encoded by codon optimized Factor VIII sequences, and methods of producing such polypeptides. The present disclosure also provides methods of treating bleeding disorders such as hemophilia comprising administering to the subject a codon optimized Factor VIII nucleic acid sequence or the polypeptide encoded thereby.
1. An isolated nucleic acid molecule comprising a nucleotide sequence encoding a polypeptide with FVIII activity, wherein the nucleotide sequence comprises a nucleic acid sequence comprising nucleotides 58-2277 and 2320-4374 of SEQ ID NO: 71.
2. The isolated nucleic acid molecule of claim 1 , wherein the nucleotide sequence further comprises a nucleic acid sequence encoding a signal peptide, wherein the nucleic acid sequence encoding a signal peptide comprises at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100% sequence identity to:
(i) nucleotides 1 to 57 of SEQ ID NO: 1;
(ii) nucleotides 1 to 57 of SEQ ID NO: 2;
(iii) nucleotides 1 to 57 of SEQ ID NO: 3;
(iv) nucleotides 1 to 57 of SEQ ID NO: 4;
(v) nucleotides 1 to 57 of SEQ ID NO: 5;
(vi) nucleotides 1 to 57 of SEQ ID NO: 6;
(vii) nucleotides 1 to 57 of SEQ ID NO: 70;
(viii) nucleotides 1 to 57 of SEQ ID NO: 71; or
(ix) nucleotides 1 to 57 of SEQ ID NO: 68.
3. The isolated nucleic acid molecule of claim 1 , wherein the nucleic acid molecule comprises one or more property selected from the group consisting of:
(a) the human codon adaptation index of the nucleic acid molecule or a portion thereof is increased relative to SEQ ID NO: 16;
(b) the frequency of optimal codons of the nucleotide sequence or a portion thereof is increased relative to SEQ ID NO:16;
(c) the nucleotide sequence or a portion thereof contains a higher percentage of G/C nucleotides compared to the percentage of G/C nucleotides in SEQ ID NO: 16;
(d) the relative synonymous codon usage of the nucleotide sequence or a portion thereof is increased relative to SEQ ID NO: 16;
(e) the effective number of codons of the nucleotide sequence or a portion thereof is reduced relative SEQ ID NO: 16;
(f) the nucleotide sequence contains fewer nuclear matrix attachment regions/autonomously replicating sequences (MARS/ARS) relative to SEQ ID NO: 16;
(g) the nucleotide sequence contains fewer destabilizing elements relative to SEQ ID NO: 16; and
(h) any combination thereof.
4. The isolated nucleic acid molecule of claim 1 , wherein the FVIII polypeptide is a full length FVIII or a B domain deleted FVIII.
5. A vector comprising the nucleic acid molecule of claim 1 .
6. A method of increasing expression of a polypeptide with FVIII activity in a mammalian subject comprising administering to said subject a vector comprising the isolated nucleic acid molecule of claim 1 , wherein the expression of the polypeptide is increased relative to a reference nucleic acid molecule comprising SEQ ID NO: 16 or the vector comprising the reference nucleic acid molecule.
7. A method of treating hemophilia A in a mammalian subject comprising administering to said subject a vector comprising the nucleic acid molecule of claim 1 .
8. An isolated nucleic acid molecule comprising a nucleotide sequence encoding a polypeptide with FVIII activity, wherein the nucleotide sequence comprises a nucleic acid sequence comprising SEQ ID NO: 72.
9. A vector comprising the nucleic acid molecule of claim 8 .
10. The vector of claim 9 , wherein the vector is a lentiviral vector.
11. A method of increasing expression of a polypeptide with FVIII activity in a mammalian subject comprising administering to said subject a vector comprising the isolated nucleic acid molecule of claim 8 , wherein the expression of the polypeptide is increased relative to a reference nucleic acid molecule comprising SEQ ID NO: 16 or the vector comprising the reference nucleic acid molecule.
12. A method of treating hemophilia A in a mammalian subject comprising administering to said subject a vector comprising the nucleic acid molecule of claim 8 .
13. A method of treating hemophilia A in a mammalian subject comprising administering to said subject the vector of claim 10 .
14. The vector of claim 5 , wherein the vector is a lentiviral vector.
15. A method of treating hemophilia A in a mammalian subject comprising administering to said subject the vector of claim 14 .