Variant Cas9 polypeptides comprising internal insertions
The present disclosure provides variant Cas9 polypeptides, where a variant Cas9 polypeptide of the present disclosure comprises an internal insertion of a heterologous polypeptide. The present disclosure provides nucleic acids comprising nucleotide sequences encoding the variant Cas9 polypeptides. The present disclosure provides host cells comprising a variant Cas9 polypeptide of the present disclosure, or comprising a nucleic acid encoding a variant Cas9 polypeptide of the present disclosure. The present disclosure provides methods of binding and/or modifying a target nucleic acid, involving use of a variant Cas9 polypeptide of the present disclosure.
1. A Cas9 fusion polypeptide comprising:
(a) a Cas9 polypeptide; and
(b) a heterologous amino acid or heterologous polypeptide inserted internally within the Cas9 polypeptide,
wherein the heterologous amino acid or heterologous polypeptide is inserted at a position that is immediately adjacent and C-terminal, or that is immediately adjacent and N-terminal, to an amino acid residue corresponding to a residue selected from 3, 4, 42, 719, 721, 724, 940, 941, 944, 947, 952, 1010, 1011, 1012, 1015, 1016, 1022, 1026, 1027, 1031, 1034, 1046, 1047, 1049, 1050, 1051, 1052, 1053, 1054, 1056, 1058, 1061, 1062, 1063, 1064, 1065, 1068, 1070, 1071, and 1073 of the Cas9 protein set forth in SEQ ID NO: 5,
wherein the heterologous polypeptide confers an inducible conformational change on the Cas9 fusion polypeptide, and
wherein the Cas9 fusion polypeptide retains cleavage and/or binding activity relative to the activity of the Cas9 polypeptide without the inserted heterologous amino acid or heterologous polypeptide.
2. The Cas9 fusion polypeptide of claim 1 , wherein the heterologous polypeptide is an estrogen receptor alpha ligand binding domain (ER-LBD).
3. A cell comprising the Cas9 fusion polypeptide of claim 1 .
4. A nucleic acid comprising a nucleotide sequence that encodes the Cas9 fusion polypeptide of claim 1 .
5. A cell comprising the nucleic acid of claim 4 .
6. A Cas9 fusion polypeptide comprising:
(a) a Cas9 polypeptide; and
(b) a heterologous amino acid or heterologous polypeptide inserted internally within the Cas9 polypeptide,
wherein the heterologous amino acid or heterologous polypeptide is inserted at a position that is immediately adjacent and C-terminal, or that is immediately adjacent and N-terminal, to an amino acid residue corresponding to a residue selected from 4, 193, 202, 204, 208, 209, 211, 228, 238, 460, 468, 588, 802, 804, 1027, 1052, 1058, 1064, 1071, 1156, 1191, 1243, 1244, and 1287 of the Cas9 protein set forth in SEQ ID NO: 5,
wherein the Cas9 fusion polypeptide retains cleavage and/or binding activity relative to the activity of the Cas9 polypeptide without the inserted heterologous amino acid or heterologous polypeptide.
7. A Cas9 fusion polypeptide comprising:
(a) a Cas9 polypeptide; and
(b) a heterologous amino acid or heterologous polypeptide inserted internally within the Cas9 polypeptide,
wherein the heterologous amino acid or heterologous polypeptide is inserted at a position that is immediately adjacent and C-terminal, or that is immediately adjacent and N-terminal, to an amino acid residue corresponding to a residue selected from 202, 204, 208, 209, 211, 468, 1027, 1052, 1058, and 1244 of the Cas9 protein set forth in SEQ ID NO: 5,
wherein the Cas9 fusion polypeptide retains cleavage and/or binding activity relative to the activity of the Cas9 polypeptide without the inserted heterologous amino acid or heterologous polypeptide.
8. A Cas9 fusion polypeptide comprising:
(a) a Cas9 polypeptide; and
(b) a heterologous amino acid or heterologous polypeptide inserted internally within the Cas9 polypeptide,
wherein the heterologous amino acid or heterologous polypeptide is inserted in a linker that is between the alpha helical and nuclease lobes at a position that is immediately adjacent and C-terminal, or that is immediately adjacent and N-terminal, to an amino acid residue corresponding to a residue selected from 715 and 717, of the Cas9 protein set forth in SEQ ID NO: 5,
wherein the Cas9 fusion polypeptide retains cleavage and/or binding activity relative to the activity of the Cas9 polypeptide without the inserted heterologous amino acid or heterologous polypeptide.
9. A Cas9 fusion polypeptide comprising:
(a) a Cas9 polypeptide; and
(b) a heterologous amino acid or heterologous polypeptide inserted internally within the Cas9 polypeptide,
wherein the heterologous amino acid or heterologous polypeptide is inserted in an HNH domain at a position that is immediately adjacent and C-terminal, or that is immediately adjacent and N-terminal, to an amino acid residue corresponding to a residue selected from 798, 801, 802, 804, 834, 868, and 890, of the Cas9 protein set forth in SEQ ID NO: 5,
wherein the Cas9 fusion polypeptide retains cleavage and/or binding activity relative to the activity of the Cas9 polypeptide without the inserted heterologous amino acid or heterologous polypeptide.
10. A Cas9 fusion polypeptide comprising:
(a) a Cas9 polypeptide; and
(b) a heterologous amino acid or heterologous polypeptide inserted internally within the Cas9 polypeptide,
wherein the heterologous amino acid or heterologous polypeptide is inserted at a position that is immediately adjacent and C-terminal, or that is immediately adjacent and N-terminal, to an amino acid residue corresponding to residue 231 of the Cas9 protein set forth in SEQ ID NO: 5,
wherein the Cas9 fusion polypeptide retains cleavage and/or binding activity relative to the activity of the Cas9 polypeptide without the inserted heterologous amino acid or heterologous polypeptide.
11. A method of binding a target nucleic acid, comprising:
contacting a target nucleic acid with: (i) a Cas9 fusion polypeptide of claim 1 , and (ii) a Cas9 guide RNA.
12. The method of claim 11 , wherein the Cas9 fusion polypeptide modulates transcription from the target nucleic acid, modifies the target nucleic acid, or cleaves the target nucleic acid.
13. The method of claim 11 , wherein the method further comprises contacting the target nucleic acid with a donor template polynucleotide.
14. A method of binding a target nucleic acid, the comprising introducing into a cell: i) a DNA or RNA encoding a Cas9 fusion polypeptide of claim 1 ; ii) a DNA encoding a Cas9 guide RNA; or iii) a combination thereof.