IP Library Granted Patent US 9,907,863
Granted Patent B2
US 9,907,863 · App. 14/951,240 · Granted Mar 6, 2018

Compositions and methods for the expression of CRISPR guide RNAs using the H1 promoter

Inventors: Vinod Jaskula-Ranga (Baltimore, MD); Donald Zack (Baltimore, MD)
Assignee: The Johns Hopkins University
A61K48/0066C12N15/1138C12N15/63C12N15/85C12N15/907C07K2319/10C07K2319/60C12N2310/10C12N2310/20C12N2330/51C12N2750/14133C12N2750/14143C12N2830/85
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Quick Facts
Patent No.
US 9,907,863
App. No.
14/951,240
Granted
Mar 6, 2018
Kind
B2
Abstract

The presently disclosed subject matter provides compositions and methods for the expression of CRISPR guide RNAs using the H1 promoter. In particular, compositions and methods are provided for the use of the H1 promoter to express CRISPR guide RNA (gRNA) with altered specificity of the 5′ nucleotide, as well as use of the H1 promoter sequence as a bidirectional promoter to express Cas9 nuclease and the gRNA simultaneously. Compositions and methods are also provided for the expression and regulation of gRNA expression in vivo through the use of RNA ribozymes and regulatable aptazymes.

Claims (9)

1. A method, the method comprising introducing into a cell a non-naturally occurring CRISPR-Cas system comprising a single vector comprising an H1 bidirectional promoter, wherein the H1 bidirectional promoter comprises:

a) control elements that provide for transcription in one direction of at least one nucleotide sequence encoding a CRISPR-Cas system guide RNA (gRNA), wherein the gRNA hybridizes with a target sequence of the DNA molecule; and

b) control elements that provide for transcription in the opposite direction of a nucleotide sequence encoding a RNA-directed nuclease,

wherein the gRNA targets and hybridizes with the target sequence and directs the RNA-directed nuclease to the DNA molecule, and wherein said system is packaged into a single adeno-associated virus (AAV) particle.

2. The method of claim 1 , wherein the target sequence comprises the nucleotide sequence AN 19 NGG, GN 19 NGG, CN 19 NGG, or TN 19 NGG.

3. The method of claim 1 , wherein the RNA-directed nuclease is a Cas9 protein.

4. The method of claim 3 , wherein the Cas9 protein is codon optimized for expression in the cell and/or is a Type-II Cas9 protein.

5. The method of claim 1 , wherein the cell is a eukaryotic cell optionally selected from the group consisting of (i) a mammalian cell, (ii) a human cell, and/or (iii) a retinal photoreceptor cell.

6. The method of claim 1 , wherein the expression of one or more gene products is decreased.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 19, 2017
From: JASKULA-RANGA, VINOD; ZACK, DONALD
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 044431/0058 →
Continuity (3)
Continuation PCTUS2015035964 · Jun 16, 2015
Provisional Application 62012802 · Jun 16, 2014
Related Publication 20160074535A1 · Mar 17, 2016