Delivery and use of the CRISPR-CAS systems, vectors and compositions for hepatic targeting and therapy
The invention provides for delivery, engineering and optimization of systems, methods, and compositions for manipulation of sequences and/or activities of target sequences. Provided are delivery systems and tissues of organ which are targeted as sites for delivery. Also 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 provide dare methods of directing CRISPR complex formation in eukaryotic cells to ensure enhanced specificity for target recognition and avoidance of toxicity and to edit or modify a target site in a genomic locus of interest to alter or improve the status of a disease or a condition.
1. A method of modifying a mammalian subject by editing in vivo a DNA target sequence in a genomic locus of interest of a hepatic cell in the mammalian subject, said method comprising in vivo delivering to the hepatic cell a single dose of a composition comprising a stable nucleic acid-lipid particle (SNALP) comprising a CRISPR-Cas system, wherein the CRISPR-Cas system comprises:
I. a CRISPR-Cas system RNA comprising a guide sequence that hybridizes to the DNA target sequence, and
II. a Cas9 comprising at least one nuclear localization sequence (NLS) or an mRNA encoding the Cas9,
wherein the guide sequence directs sequence-specific binding of a CRISPR complex to the DNA target sequence, the CRISPR complex comprises the Cas9 complexed with the CRISPR-Cas system RNA, and wherein the CRISPR complex introduces a double-stranded break in vivo in the DNA target sequence in the genomic locus of interest of the hepatic cell which forms a targeted indel in the genomic locus of interest and produces a phenotypic change in said mammalian subject, and wherein the delivering results in greater than 20% indel formation in the genomic locus of interest of the hepatic cell.
2. The method of claim 1 , wherein the Cas9 is S. pyogenes Cas9.
3. The method of claim 1 , wherein the Cas9 is S. aureus Cas9.
4. The method of claim 1 , wherein the CRISPR-Cas system RNA is a chimeric RNA (chiRNA) comprising the guide sequence fused to a tracr-mate sequence and a tracr-sequence.
5. The method of claim 1 , wherein the DNA target sequence is adjacent to a protospacer adjacent motif (PAM).
6. The method of claim 5 , wherein the PAM is 5′-NRG.
7. The method of claim 5 , wherein the PAM is 5′-NNGRR.
8. The method of claim 1 , wherein the composition comprises the CRISPR-Cas system RNA and the Cas9.
9. The method of claim 1 , wherein the composition comprises the CRISPR-Cas system RNA and the mRNA encoding the Cas9.
10. The method of claim 1 , wherein the composition comprises two or more CRISPR-Cas system RNAs each hybridizing to a different DNA target sequence.
11. The method of claim 1 , wherein the delivering comprises injecting the composition into the mammalian subject.
12. The method of claim 11 , wherein injecting comprises intravenous injection, stereotactic injection, or intramuscular injection.
13. The method of claim 1 , wherein the mammalian subject is a human subject.
14. The method of claim 1 , wherein the SNALP comprises cholesterol and PEG-lipid.
15. A method of modifying a mammalian subject by editing in vivo a DNA target sequence in a genomic locus of interest of a hepatic cell in the mammalian subject, said method comprising in vivo delivering to the hepatic cell a single dose of a composition comprising a stable nucleic acid-lipid particle (SNALP) comprising a CRISPR-Cas system, wherein the CRISPR-Cas system comprises:
I. a CRISPR-Cas system RNA comprising a guide sequence that hybridizes to the DNA target sequence, and
II. a Cas9 comprising at least one nuclear localization sequence (NLS) or an mRNA encoding the Cas9,
wherein the guide sequence directs sequence-specific binding of a CRISPR complex to the DNA target sequence, the CRISPR complex comprises the Cas9 complexed with the CRISPR-Cas system RNA, and wherein the CRISPR complex introduces a double-stranded break in vivo in the DNA target sequence in the genomic locus of interest of the hepatic cell which forms a targeted indel in the genomic locus of interest and produces a phenotypic change in said mammalian subject, and wherein the Cas9 is S. aureus Cas9.
16. A method of modifying a mammalian subject by editing in vivo a DNA target sequence in a genomic locus of interest of a hepatic cell in the mammalian subject, said method comprising in vivo delivering to the hepatic cell a single dose of a composition comprising a stable nucleic acid-lipid particle (SNALP) comprising a CRISPR-Cas system, wherein the CRISPR-Cas system comprises:
I. a CRISPR-Cas system RNA comprising a guide sequence that hybridizes to the DNA target sequence, and
II. a Cas9 comprising at least one nuclear localization sequence (NLS) or an mRNA encoding the Cas9,
wherein the guide sequence directs sequence-specific binding of a CRISPR complex to the DNA target sequence, the CRISPR complex comprises the Cas9 complexed with the CRISPR-Cas system RNA, and wherein the CRISPR complex introduces a double-stranded break in vivo in the DNA target sequence in the genomic locus of interest of the hepatic cell which forms a targeted indel in the genomic locus of interest and produces a phenotypic change in said mammalian subject, and wherein the DNA target sequence is adjacent to a protospacer adjacent motif (PAM) and the PAM is 5′-NNGRR.