Modified tracrRNAs gRNAs, and uses thereof
Provided are compositions and methods for altering gene expression in cells. The compositions and methods may utilize a nucleic acid sequence that has a genetically modified trans-activating crRNA (tracrRNA) sequence, where at least one uracil nucleotide of the tracrRNA sequence is replaced with a nucleotide other than uracil, and/or a nucleic acid sequence that has a guide RNA (gRNA) sequence wherein one or more cytosine nucleotides and/or one or more uracil nucleotides of said gRNA sequence are modified nucleotides. Also provided are methods of treating a disorder in a subject in need of the treatment. The method may involve administering to the subject the nucleic acid or a vector thereof in combination with an RNA-guided DNA endonuclease enzyme.
1. A nucleic acid comprising a trans-activating crRNA (tracrRNA) sequence, wherein the tracrRNA sequence is SEQ ID NO: 171, SEQ ID NO: 203, or SEQ ID NO: 223.
2. A composition comprising: (a) a first nucleic acid comprising a trans-activating crRNA (tracrRNA) sequence, wherein the tracrRNA sequence is SEQ ID NO: 171, SEQ ID NO: 203, or SEQ ID NO: 223; and (b) a second nucleic acid comprising a guide RNA (gRNA) sequence, wherein one or more cytosine nucleotides and/or one or more uracil nucleotides of said gRNA sequence are modified nucleotides.
3. The composition of claim 2 , further comprising an RNA-guided DNA endonuclease enzyme or a pharmaceutically acceptable excipient.
4. The composition of claim 3 , wherein:
(a) said RNA-guided DNA endonuclease enzyme is Cas9 or Cpf1 or a Class II CRISPR endonuclease or a variant thereof;
(b) said RNA-guided DNA endonuclease enzyme is a modified Cas endonuclease; or
(c) said RNA-guided DNA endonuclease enzyme is deactivated Cas9 (dCas9) or mutated Cas9 nickase (D10A).
5. A vector comprising or encoding the nucleic acid of claim 1 .
6. A pharmaceutical composition comprising (a) the nucleic acid of claim 1 , or a vector comprising or encoding the nucleic acid, and (b) a pharmaceutically acceptable excipient.
7. A method of altering gene expression in a cell, the method comprising introducing into said cell the nucleic acid of claim 1 .
8. The method of claim 7 , furthering comprising introducing to said cell an RNA-guided DNA endonuclease enzyme.
9. The method of claim 8 , wherein:
(a) said RNA-guided DNA endonuclease enzyme is Cas9 or Cpf1 or a Class II CRISPR endonuclease or a variant thereof;
(b) said RNA-guided DNA endonuclease enzyme is a modified Cas endonuclease;
(c) said RNA-guided DNA endonuclease enzyme is deactivated Cas9 (dCas9) or mutated Cas9 nickase (D10A);
(d) said RNA-guided DNA endonuclease enzyme is a conjugate comprising a Cas 9 endonuclease and a transcription regulating factor; or
(e) said RNA-guided DNA endonuclease enzyme comprises a dCas-APOBEC3A fusion protein, a dCas-VPR fusion protein or a dCas-KRAB fusion protein.
10. A method of treating a disorder in a subject in need thereof, the method comprising administering to said subject: (a) the nucleic acid of claim 1 ; and (b) an RNA-guided DNA endonuclease enzyme; optionally wherein said disorder is HIV, cancer, COPD, Cystic Fibrosis, heart conditions/repair, and diabetes.
11. The nucleic acid of claim 1 , wherein the tracrRNA sequence is SEQ ID NO: 171.
12. The nucleic acid of claim 1 , wherein the tracrRNA sequence is SEQ ID NO: 203.
13. The nucleic acid of claim 1 , wherein the tracrRNA sequence is SEQ ID NO: 223.
14. The composition of claim 2 , wherein the tracrRNA sequence is SEQ ID NO: 171.
15. The composition of claim 2 , wherein the tracrRNA sequence is SEQ ID NO: 203.
16. The composition of claim 2 , wherein the tracrRNA sequence is SEQ ID NO: 223.