GENOMIC EDITING OF GENES INVOLVED IN AUTISM SPECTRUM DISORDERS
The present invention provides genetically modified animals and cells comprising edited chromosomal sequences encoding proteins associated with ASD. In particular, the animals or cells are generated using a zinc finger nuclease-mediated editing process. Also provided are methods of using the genetically modified animals or cells disclosed herein to study ASD development and screen agents for assessing their effect on progression or symptoms of an ASD.
1 . A genetically modified animal comprising at least one edited chromosomal sequence encoding a protein associated with ASD.
2 . The genetically modified animal of claim 1 , wherein the edited chromosomal sequence is inactivated, modified, or comprises an integrated sequence.
3 . The genetically modified animal of claim 1 , wherein the edited chromosomal sequence is inactivated such that no functional protein associated with ASD associated is produced.
4 . The genetically modified animal of claim 3 , wherein inactivated chromosomal sequence comprises no exogenously introduced sequence.
5 . The genetically modified animal of claim 3 , further comprising at least one chromosomally integrated sequence encoding a functional protein associated with ASD.
6 . The genetically modified animal of claim 1 , wherein the protein associated with ASD is chosen from BZRAP1, AFF2, FXR1, FXR2, MDGA2, MECP2, MGLUR5, NRXN1, SEMA5A, and combinations thereof.
7 . The genetically modified animal of claim 1 , further comprising a conditional knock-out system for conditional expression of the protein associated with ASD.
8 . The genetically modified animal of claim 1 , wherein the edited chromosomal sequence comprises an integrated reporter sequence.
9 . The genetically modified animal of claim 1 , wherein the animal is heterozygous or homozygous for the at least one edited chromosomal sequence.
10 . The genetically modified animal of claim 1 , wherein the animal is an embryo, a juvenile, or an adult.
11 . The genetically modified animal of claim 1 , wherein the animal is chosen from bovine, canine, equine, feline, ovine, porcine, non-human primate, and rodent.
12 . The genetically modified animal of claim 1 , wherein the animal is rat.
13 . The genetically modified animal of claim 4 , wherein the animal is rat and the protein is an ortholog of a human protein associated with ASD.
14 . A non-human embryo, the embryo comprising at least one RNA molecule encoding a zinc finger nuclease that recognizes a chromosomal sequence encoding a protein associated with ASD, and, optionally, at least one donor polynucleotide comprising a sequence encoding an ortholog of the protein associated with ASD or an edited protein associated with ASD.
15 . The non-human embryo of claim 14 , wherein the protein associated with ASD is chosen from BZRAP1, AFF2, FXR1, FXR2, MDGA2, MECP2, MGLUR5, NRXN1, SEMA5A, and combinations thereof.
16 . The non-human embryo of claim 14 , wherein the embryo is chosen from bovine, canine, equine, feline, ovine, porcine, non-human primate, and rodent.
17 . The non-human embryo of claim 14 , wherein the embryo is rat and the protein is an ortholog of a human protein associated with ASD.
18 . A genetically modified cell, the cell comprising at least one edited chromosomal sequence encoding a protein associated with ASD.
19 . The genetically modified cell of claim 18 , wherein the edited chromosomal sequence is inactivated, modified, or comprises an integrated sequence.
20 . The genetically modified cell of claim 19 , wherein the edited chromosomal sequence is inactivated such that the protein associated with ASD is not produced or is not functional.
21 . The genetically modified cell of claim 20 , further comprising at least one chromosomally integrated sequence encoding a functional protein associated with ASD.
22 . The genetically modified cell of claim 18 , wherein the protein associated with ASD is chosen from BZRAP1, AFF2, FXR1, FXR2, MDGA2, MECP2, MGLUR5, NRXN1, SEMA5A, and combinations thereof.
23 . The genetically modified cell of claim 18 , wherein the cell is heterozygous or homozygous for the at least one edited chromosomal sequence.
24 . The genetically modified cell of claim 18 , wherein the cell is of bovine, canine, equine, feline, human, ovine, porcine, non-human primate, or rodent origin.
25 . The genetically modified cell of claim 18 , wherein the cell is of rat origin and the protein is an ortholog of a human protein associated with ASD.
26 . A method for assessing the effect of an agent in a genetically modified animal, the method comprising administering the agent to the genetically modified animal comprising at least one edited chromosomal sequence encoding a protein associated with ASD, and comparing a parameter obtained from the genetically modified animal to the parameter obtained from a wild-type animal administered the same agent, wherein the parameter is chosen from:
a) rate of elimination of the agent or its metabolite(s);
b) circulatory levels of the agent or its metabolite(s);
c) bioavailability of the agent or its metabolite(s);
d) rate of metabolism of the agent or its metabolite(s);
e) rate of clearance of the agent or its metabolite(s);
f) toxicity of the agent or its metabolite(s); and
g) ability of the agent to modify an incidence or indication of an ASD in the genetically modified animal.
27 . The method of claim 26 , wherein the agent is a pharmaceutically active ingredient, a drug, a toxin, or a chemical.
28 . The method of claim 26 , wherein the at least one edited chromosomal sequence is inactivated such that the protein associated with ASD is not produced or is not functional, and wherein the genetically modified animal further comprises at least one chromosomally integrated sequence encoding a functional ortholog of the protein associated with ASD.
29 . The method of claim 26 , wherein the protein associated with ASD is chosen from BZRAP1, AFF2, FXR1, FXR2, MDGA2, MECP2, MGLUR5, NRXN1, SEMA5A, and combinations thereof.
30 . The method of claim 26 , wherein the animal is a rat of a strain chosen from Dahl Salt-Sensitive, Fischer 344, Lewis, Long Evans Hooded, Sprague-Dawley, and Wistar.
31 . The method of claim 26 , wherein the incidence or indication of the ASD occurs spontaneously in the genetically modified animal.
32 . The method of claim 26 , wherein the incidence or indication of the ASD is promoted by exposure to a disruptive agent.
33 . The method of claim 36 , wherein the disruptive agent is chosen from a protein associated with ASD, a drug, a toxin, a chemical, an activated retrovirus, and an environmental stress.
34 . A method for assessing the therapeutic potential of an agent as a treatment for an ASD, the method comprising administering the agent to a genetically modified animal, wherein the genetically modified animal comprises at least one edited chromosomal sequence encoding a protein associated with ASD, and comparing a selected parameter obtained from the genetically modified animal to the selected parameter obtained from a wild-type animal with no exposure to the same agent, wherein the selected parameter is chosen from:
a) spontaneous behaviors;
b) performance during behavioral testing;
c) physiological anomalies;
d) abnormalities in tissues or cells;
e) biochemical function; and
f) molecular structures.
35 . The method of claim 34 , wherein the agent comprises at least one pharmaceutically active compound.
36 . The method of claim 34 , wherein the at least one edited chromosomal sequence is inactivated such that the protein associated with ASD is not produced or is not functional, and wherein the animal further comprises at least one chromosomally integrated sequence encoding a functional ortholog of the protein associated with ASD.
37 . The method of claim 34 , wherein the protein associated with ASD is chosen from BZRAP1, AFF2, FXR1, FXR2, MDGA2, MECP2, MGLUR5, NRXN1, SEMA5A, and combinations thereof.
38 . The method of claim 34 , wherein the animal is a rat of a strain chosen from Dahl Salt-Sensitive, Fischer 344, Lewis, Long Evans Hooded, Sprague-Dawley, and Wistar.
39 . The method of claim 34 , wherein the incidence or indication of the ASD occurs spontaneously in the genetically modified animal.
40 . The method of claim 34 , wherein the incidence or indication of the ASD is promoted by exposure to a disruptive agent.
41 . The method of claim 40 , wherein the disruptive agent is chosen from a protein associated with ASD, a drug, a toxin, a chemical, an activated retrovirus, and an environmental stress.