Method of inactivating a glucocorticoid receptor gene in an isolated cell
Disclosed herein are methods and compositions for inactivation of the human glucocorticoid receptor (GR) gene by targeted cleavage of genomic DNA encoding the GR. Such methods and compositions are useful, for example, in therapeutic applications which require retention of immune function during glucocorticoid treatment.
1. A method of selecting isolated human cells comprising a transgene integrated into an endogenous glucocorticoid receptor (GR) gene, the method comprising:
a) introducing:
i) one or more polynucleotides encoding a first and second pair of zinc finger nuclease (ZFN); and
ii) a polynucleotide comprising a transgene flanked by homology arms that target a human glucocorticoid receptor (GR) gene into isolated human cells such that the transgene is integrated into an endogenous GR gene,
wherein
the first ZFN comprises:
a zinc finger DNA-binding domain comprising the following recognition helices in the following order:
(SEQ ID NO: 23)
TSRALTA;
(SEQ ID NO: 17)
DRANLSR;
(SEQ ID NO: 24)
RSDNLSE;
and
(SEQ ID NO: 26)
ERANRNS;
and
the second ZFN comprises:
a zinc finger DNA-binding domain comprising the following recognition helices in the following order:
(SEQ ID NO: 33)
DSWNLQV;
(SEQ ID NO: 27)
RSANLTR;
(SEQ ID NO: 30)
TSGNLTR;
and
(SEQ ID NO: 31)
TSGSLTR;
or
the first ZFN comprises:
a zinc finger DNA-binding domain comprising the following recognition helices in the following order:
(SEQ ID NO: 42)
RSANLAR;
(SEQ ID NO: 43)
RSDNLRE;
(SEQ ID NO: 44)
QSSNLAR;
and
(SEQ ID NO: 45)
QSADRTK;
and
the second ZFN comprises:
a zinc finger DNA-binding domain comprising the following recognition helices in the following order:
(SEQ ID NO: 40)
RQDCLSL;
(SEQ ID NO: 37)
RNDNRKT;
(SEQ ID NO: 38)
RSDNLSR;
and
(SEQ ID NO: 39)
TNQNRIT;
and
b) contacting the isolated human cells obtained in step a) with a corticosteroid such that cells not comprising the integrated transgene are killed and cells comprising the transgene integrated into the endogenous GR gene are selected.
2. The method of claim 1 , wherein the corticosteroid is synthetic.
3. The method of claim 2 , wherein the corticosteroid is dexamethasone.
4. The method of claim 1 , wherein the introducing step comprises introducing a viral vector comprising the one or more polynucleotides encoding the first and second ZFN or the polynucleotide comprising the transgene.
5. The method of claim 4 , wherein the viral vector is replication-defective.
6. The method of claim 4 , wherein the viral vector is an adenovirus, a hybrid adenovirus, or a non-integrating lentivirus.
7. The method of claim 1 , wherein the first ZFN comprises a zinc finger DNA-binding domain comprising the following recognition helices in the following order:
(SEQ ID NO: 23)
TSRALTA;
(SEQ ID NO: 17)
DRANLSR;
(SEQ ID NO: 24)
RSDNLSE;
and
(SEQ ID NO: 26)
ERANRNS;
and
the second ZFN comprises a zinc finger DNA-binding domain comprising the following recognition helices in the following order:
(SEQ ID NO: 33)
DSWNLQV;
(SEQ ID NO: 27)
RSANLTR;
(SEQ ID NO: 30)
TSGNLTR;
and
(SEQ ID NO: 31)
TSGSLTR.
8. The method of claim 7 , wherein the corticosteroid is synthetic.
9. The method of claim 7 , wherein the corticosteroid is dexamethasone.
10. The method of claim 7 , wherein the introducing step comprises introducing a viral vector comprising the one or more polynucleotides encoding the first and second ZFN or the polynucleotide comprising the transgene.
11. The method of claim 10 , wherein the viral vector is replication-defective.
12. The method of claim 7 , wherein the viral vector is an adenovirus, a hybrid adenovirus, or a non-integrating lentivirus.