Novel crispr dna targeting enzymes and systems

Abstract

The disclosure describes novel systems, methods, and compositions for the manipulation of nucleic acids in a targeted fashion. The disclosure describes non-naturally occurring, engineered CRISPR systems, components, and methods for targeted modification of nucleic acids such as DNA. Each system includes one or more protein components and one or more nucleic acid components that together target nucleic acids.

What is claimed is: 
     
         1 . An engineered, non-naturally occurring Clustered Regularly Interspaced Short Palindromic Repeat (CRISPR)-associated (Cas) system comprising:
 (a) an RNA guide or a nucleic acid encoding the RNA guide, wherein the RNA guide comprises a direct repeat sequence and a spacer sequence, wherein the direct repeat sequence comprises 5′-CCGUCNNNNNNUGACGG-3′ (SEQ ID NO: 202), wherein N is any nucleobase; and   (b) a CRISPR-Cas effector protein or a nucleic acid encoding the CRISPR-Cas effector protein,   wherein the CRISPR-Cas effector protein binds to the RNA guide, and wherein the spacer sequence binds to a target nucleic acid.   
     
     
         2 . The system of  claim 1 , wherein SEQ ID NO: 202 is proximal to the 3′ end of the direct repeat sequence. 
     
     
         3 . The system of  claim 1 , wherein the direct repeat sequence comprises a stem-loop structure proximal to a 3′ end of the direct repeat sequence, wherein the stem-loop structure comprises:
 (a) a first stem nucleotide strand 5 nucleotides in length; 
 (b) a second stem nucleotide strand 5 nucleotides in length, wherein the first and second stem nucleotide strands bind with each other; and 
 (c) a loop nucleotide strand arranged between the first and second stem nucleotide strands, wherein the loop nucleotide strand comprises 6, 7, or 8 nucleotides. 
 
     
     
         4 . The system of  claim 1 , wherein the direct repeat sequence comprises an RNA transcript of a nucleotide sequence with at least 95% sequence identity to SEQ ID NO: 9 or SEQ ID NO: 10. 
     
     
         5 . The system of  claim 1 , wherein the direct repeat sequence comprises an RNA transcript of a nucleotide sequence set forth in SEQ ID NO: 9 or SEQ ID NO: 10. 
     
     
         6 . The system of  claim 1 , wherein the RNA guide comprises a nucleotide sequence with at least 95% sequence identity to SEQ ID NO: 162 or SEQ ID NO: 163 or a fragment thereof. 
     
     
         7 . The system of  claim 1 , wherein the RNA guide comprises a nucleotide sequence set forth in to SEQ ID NO: 162 or SEQ ID NO: 163 or a fragment thereof. 
     
     
         8 . The system of  claim 1 , wherein the RNA guide comprises a nucleotide sequence with at least 95% sequence identity to SEQ ID NO: 101. 
     
     
         9 . The system of  claim 1 , wherein the RNA guide comprises a nucleotide sequence set forth in SEQ ID NO: 101. 
     
     
         10 . The system of  claim 1 , wherein the spacer sequence comprises between 15 and 47 nucleotides in length. 
     
     
         11 . The system of  claim 10 , wherein the spacer sequence comprises between 24 and 38 nucleotides in length or between 20 and 33 nucleotides in length. 
     
     
         12 . The system of  claim 1 , wherein the spacer sequence has at least 90%, 95%, or 100% complementarity to the target nucleic acid. 
     
     
         13 . The system of  claim 1 , wherein the system does not include a tracrRNA. 
     
     
         14 . The system of  claim 1 , wherein the CRISPR-Cas effector protein comprises one or more of:
 (a) a RuvC domain comprising the amino acid sequence X 1 SHX 4 DX 6 X 7 (SEQ ID NO: 200), wherein X 1  is S or T, X 4  is Q or L, X 6  is P or S, and X, is F or L,   (b) a RuvC domain comprising the amino acid sequence X 1 XDXNX 6 X 7 XXXX 11  (SEQ ID NO: 201), wherein X, is A, G, or S, X is any amino acid, X 6  is Q or I, X, is T, S, or V, and X 10  is T or A; and   (c) a RuvC domain comprising the amino acid sequence X 1 X 2 X 3 E (SEQ ID NO: 210), wherein X 1  is C, F, I, L, M, P, V, W, or Y, X 2  is C, F, I, L, M, P, R, V, W, or Y, and X 3  is C, F, G, I, L, M, P, V, W, or Y.   
     
     
         15 . The system of  claim 1 , wherein the CRISPR-Cas effector protein comprises an amino acid sequence with at least 95% identity to SEQ ID NO: 5. 
     
     
         16 . The system of  claim 1 , wherein the CRISPR-Cas effector protein comprises the amino acid sequence set forth in SEQ ID NO: 5. 
     
     
         17 . The system of  claim 1 , wherein the CRISPR-Cas effector protein recognizes a protospacer adjacent motif (PAM) sequence, wherein the PAM sequence comprises a nucleotide sequence set forth as 5′-TTN-3′, wherein N is any nucleotide. 
     
     
         18 . The system of  claim 17 , wherein the PAM sequence comprises a nucleotide sequence set forth as 5′-TTY-3′, wherein Y is C or T, or 5′-TTH-3′, wherein H is A or C or T. 
     
     
         19 . The system of  claim 1 , wherein the CRISPR-Cas effector protein further comprises at least one nuclear localization signal (NLS), at least one nuclear export signal (NES), or at least one NLS and at least one NES. 
     
     
         20 . The system of  claim 1 , wherein the CRISPR-Cas effector protein further comprises a peptide tag, a fluorescent protein, a base-editing domain, a DNA methylation domain, a histone residue modification domain, a localization factor, a transcription modification factor, a light-gated control factor, a chemically inducible factor, or a chromatin visualization factor. 
     
     
         21 . The system of  claim 1 , wherein the nucleic acid encoding the CRISPR-Cas effector protein is codon-optimized for expression in a cell. 
     
     
         22 . The system of  claim 1 , wherein the nucleic acid encoding the CRISPR-Cas effector protein is operably linked to a promoter. 
     
     
         23 . The system of  claim 1 , wherein the nucleic acid encoding the CRISPR-Cas effector protein is in a vector. 
     
     
         24 . The system of  claim 23 , wherein the vector comprises a retroviral vector, a lentiviral vector, a phage vector, an adenoviral vector, an adeno-associated vector, or a herpes simplex vector. 
     
     
         25 . The system of  claim 1 , wherein the system is present in a delivery system comprising a nanoparticle, a liposome, an exosome, a microvesicle, or a gene-gun. 
     
     
         26 . A cell comprising the system of  claim 1 . 
     
     
         27 . The cell of  claim 26 , wherein the cell is a prokaryotic cell or a eukaryotic cell. 
     
     
         28 . The cell of  claim 26 , wherein the cell is a mammalian cell or a plant cell. 
     
     
         29 . The cell of  claim 28 , wherein the cell is a human cell. 
     
     
         30 . A method of binding the system of  claim 1  to the target nucleic acid in a cell comprising:
 (a) providing the system; and 
 (b) delivering the system to the cell, 
 wherein the cell comprises the target nucleic acid, wherein the CRISPR-Cas effector protein binds to the RNA guide, and wherein the spacer sequence binds to the target nucleic acid. 
 
     
     
         31 . The method of  claim 30 , wherein the target nucleic acid is a single-stranded DNA or a double-stranded DNA. 
     
     
         32 . The method of  claim 30 , wherein binding the system to the target nucleic acid results in cleavage of the target nucleic acid. 
     
     
         33 . The method of  claim 32 , wherein cleavage of the target nucleic acid results in formation of an insertion or a deletion in the target nucleic acid.