Genome engineering with Type I CRISPR systems in eukaryotic cells
Disclosed herein are Type I Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated (Cas) system related compositions and methods of using said Type I CRISPR/Cas system related compositions for altering gene expression and genome engineering. The invention relates to compositions comprising Type I CRISPR-Cas polypeptides and CRISPR array nucleic acids designed for genome modification in eukaryotic cells and for targeted killing of eukaryotic cells.
1. A composition for genome engineering a target gene in a eukaryotic cell, the composition comprising:
a. a polynucleotide sequence encoding:
i. a Cascade complex comprising a Cse1 polypeptide, a Cse2 polypeptide, a Cas7 polypeptide, a Cas5 polypeptide, and a Cas6e polypeptide,
wherein the polynucleotide sequence encoding the Cse1 polypeptide comprises the polynucleotide sequence of SEQ ID NO: 23, the polynucleotide sequence encoding the Cse2 polypeptide comprises the polynucleotide sequence of SEQ ID NO: 24, the polynucleotide sequence encoding the Cas7 polypeptide comprises the polynucleotide sequence of SEQ ID NO: 25, the polynucleotide sequence encoding the Cas5 polypeptide comprises the polynucleotide sequence of SEQ ID NO: 26, and the polynucleotide sequence encoding the Cas6e polypeptide comprises the polynucleotide sequence of SEQ ID NO: 27; and
ii. a polypeptide domain, wherein the polypeptide domain comprises transcription activation activity, transcription repression activity, transcription release factor activity, histone modification activity, nuclease activity, nucleic acid association activity, methylase activity, or demethylase activity; and
b. a pharmaceutically acceptable carrier.
2. The composition of claim 1 , wherein the polypeptide domain is fused to a N terminus or a C terminus of the Cse1 polypeptide, the Cse2 polypeptide, the Cas7 polypeptide, the Cas5 polypeptide, or the Cas6e polypeptide of the Cascade complex.
3. The composition of claim 1 , wherein the Cascade complex is associated with the polypeptide domain via a linker.
4. The composition of claim 1 , wherein the polypeptide domain has transcription activation activity.
5. The composition of claim 4 , wherein the polypeptide domain comprises at least one VP16 transcription activation domain repeat.
6. The composition of claim 4 , wherein the polypeptide domain comprises a p300 core domain, VP16 tetramer (“VP64”), or a p65 activation domain.
7. The composition of claim 1 , wherein the polypeptide domain has transcription repression activity.
8. The composition of claim 7 , wherein the polypeptide domain comprises a KRAB domain.
9. The composition of claim 1 , wherein the polypeptide domain has methylase activity.
10. The composition of claim 1 , wherein the polypeptide domain has demethylase activity.
11. The composition of claim 1 , wherein the polynucleotide sequence further encodes a Cas3 polypeptide.
12. The composition of claim 11 , wherein the Cas3 polypeptide is mutated such that the helicase, and/or exonuclease activity is inactivated.
13. The composition of claim 1 , wherein the polynucleotide sequence further encodes a crRNA, wherein the crRNA targets a target nucleotide sequence from the target gene.
14. The composition of claim 1 , wherein the polynucleotide sequence is operably linked to a eukaryotic promoter.
15. The composition of claim 11 , wherein the Cas3 polypeptide comprises the amino acid sequence of SEQ ID NO: 15, SEQ ID NO: 17, or SEQ ID NO: 19.
16. A method of killing a eukaryotic cell, the method comprising introducing into the eukaryotic cell the composition of claim 1 .
17. The method of claim 16 , wherein the polynucleotide sequence further encodes a Cas3 polypeptide.