CRISPR-Cas component systems, methods and compositions for sequence manipulation
The invention provides for systems, methods, and compositions for manipulation of sequences and/or activities of target sequences. Provided are vectors and vector systems, some of which encode one or more components of a CRISPR complex, as well as methods for the design and use of such vectors. Also provided are methods of directing CRISPR complex formation in eukaryotic cells and methods for selecting specific cells by introducing precise mutations utilizing the CRISPR/Cas system.
1. A method of altering expression of at least one gene product comprising
introducing into a eukaryotic cell containing and expressing a DNA molecule having a target sequence and encoding the gene product an engineered, non-naturally occurring Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-CRISPR associated (Cas) system comprising one or more vectors comprising:
a) a first regulatory element operable in a eukaryotic cell operably linked to at least one nucleotide sequence encoding a CRISPR-Cas system guide RNA that hybridizes with the target sequence, and
b) a second regulatory element operable in a eukaryotic cell operably linked to a nucleotide sequence encoding a Type-II Cas9 protein,
wherein components (a) and (b) are located on same or different vectors of the system,
wherein the CRISPR-Cas system comprises two or more nuclear localization signals (NLSs),
whereby the guide RNA targets the target sequence and the Cas9 protein cleaves the DNA molecule, whereby expression of the at least one gene product is altered; and, wherein the Cas9 protein and the guide RNA do not naturally occur together.
2. The method of claim 1 , wherein the expression of two or more gene products is altered.
3. The method of claim 1 , wherein the CRISPR-Cas system comprises a trans-activating cr (tracr) sequence.
4. The method of claim 1 , wherein at least one NLS is at or within 50 amino acids of the amino-terminus of the Cas9 protein and/or at least one NLS is at or within 50 amino acids of the carboxy-terminus of the Cas9 protein.
5. The method of claim 1 , wherein the one or more vectors are viral vectors.
6. The method of claim 5 , wherein the one or more viral vectors are selected from the group consisting of retroviral, lentiviral, adenoviral, adeno-associated and herpes simplex viral vectors.
7. The method of claim 1 , wherein the Cas9 protein is codon optimized for expression in the eukaryotic cell.
8. The method of claim 1 , wherein the eukaryotic cell is a mammalian or human cell.
9. The method of claim 1 , wherein the expression of one or more gene products is increased.
10. The method of claim 1 , wherein the expression of one or more gene products is decreased.
11. A CRISPR-Cas system-mediated genome editing method comprising introducing into a eukaryotic cell containing a polynucleotide having a sequence wherein the polynucleotide sequence includes a target sequence, an engineered, non-naturally occurring CRISPR-Cas system comprising one or more vectors comprising:
a) a first regulatory element operable in a eukaryotic cell operably linked to at least one nucleotide sequence encoding a CRISPR-Cas system guide RNA that hybridizes with the target sequence, and
b) a second regulatory element operable in a eukaryotic cell operably linked to a nucleotide sequence encoding a Type-II Cas9 protein,
wherein components (a) and (b) are located on same or different vectors of the system,
wherein the CRISPR-Cas system comprises two or more NLSs, whereby the polynucleotide sequence is modified through the CRISPR-Cas system directing sequence-specific genome editing; and, wherein the Cas9 protein and the guide RNA do not naturally occur together.
12. The method of claim 11 , wherein the sequence-specific genome editing comprises creation of a double strand break (DSB) which is repaired by a non-homologous end joining (NHEJ) cell repair mechanism generating indels thereby modifying the polynucleotide sequence.
13. The method of claim 11 , wherein the sequence-specific genome editing comprises creation of a DSB which is repaired by a homologous recombination (HR) cell repair mechanism incorporating a HR template into the polynucleotide thereby modifying the polynucleotide sequence.
14. The method of claim 11 , wherein at least one NLS is at or within 50 amino acids of the amino-terminus of the Cas9 protein or/and at least one NLS is at or within 50 amino acids of the carboxy-terminus of the Cas9 protein.
15. The method of claim 11 , wherein the CRISPR-Cas system comprises a tracr sequence.
16. The method of claim 11 , wherein the Cas9 protein is codon optimized for expression in the eukaryotic cell.
17. The method of claim 11 , wherein the eukaryotic cell is a mammalian or human cell.
18. An engineered, non-naturally occurring CRISPR-Cas system comprising one or more vectors comprising:
a) a first regulatory element operable in a eukaryotic cell operably linked to at least one nucleotide sequence encoding a CRISPR-Cas system guide RNA that hybridizes with a target sequence of a DNA molecule in a eukaryotic cell that contains the DNA molecule, wherein the DNA molecule encodes and the eukaryotic cell expresses at least one gene product,
b) a second regulatory element operable in a eukaryotic cell operably linked to a nucleotide sequence encoding a Type-II Cas9 protein,
wherein components (a) and (b) are located on same or different vectors of tile system,
wherein the CRISPR-Cas system comprises a tracr sequence,
wherein the CRISPR-Cas system comprises two or more nuclear localization signals (NLSs),
whereby the guide RNA targets and hybridizes with the target sequence and the Cas9 protein cleaves the DNA molecule, whereby expression of the at least one gene product is altered; and, wherein the Cas9 protein and the guide RNA do not naturally occur together.
19. The system of claim 18 , wherein at least one NLS is at or within 50 amino acids of the amino-terminus of the Cas9 protein and/or at least one NLS is at or within 50 amino acids of the carboxy-terminus of the Cas9 protein.
20. The system of claim 18 , wherein the Cas9 protein is codon optimized for expression in the eukaryotic cell.
21. The system of claim 18 , wherein the eukaryotic cell is a mammalian or human cell.
22. The system of claim 18 , wherein the expression of one or more gene products is increased.
23. The system of claim 18 , wherein the expression of one or more gene products is decreased.
24. The system of claim 18 , wherein the one or more vectors are viral vectors.
25. The system of claim 24 , wherein the one or more viral vectors are selected from the group consisting of retroviral, lentiviral, adenoviral, adeno-associated and herpes simplex viral vectors.
26. An engineered, programmable, non-naturally occurring Type II CRISPR-Cas system comprising a Cas9 protein and at least one guide RNA that targets and hybridizes to a target sequence of a DNA molecule in a eukaryotic cell, wherein the CRISPR-Cas system comprises two or more nuclear localization signals (NLSs), wherein the DNA molecule encodes and the eukaryotic cell expresses at least one gene product and the Cas9 protein cleaves the DNA molecule, whereby expression of the at least one gene product is altered; and, wherein the Cas9 protein and the guide RNA do not naturally occur together.
27. The CRISPR-Cas system of claim 26 , wherein at least one NLS is at or within 50 amino acids of the amino-terminus of the Cas9 protein and/or at least one NLS is at or within 50 amino acids of the carboxy-terminus of the Cas9 protein.
28. The CRISPR-Cas system of claim 26 , wherein the CRISPR-Cas system comprises a tracr sequence.
29. The CRISPR-Cas system of claim 26 , wherein the Cas9 protein is codon optimized for expression in the eukaryotic cell.
30. The CRISPR-Cas system of claim 26 , wherein the eukaryotic cell is a mammalian or human cell.