Addgene depositor Charles Gersbach used
paired zinc finger nucleases to remove exon 51 in DMD patient myoblasts.
Not exact matches
DNA polymorphism in the Y chromosome, examined at a 729 - base
pair intron located immediately upstream of the ZFY
zinc -
finger exon, revealed no sequence variation in a worldwide sample of 38 human males.
To genetically disrupt the CXCR4 allele, we designed a
pair of
zinc -
finger proteins (ZFPs) targeting the region of the cxcr4 gene that encodes residues Asp 187 to Val 196 in the second extracellular loop (ECL2) of this seven - transmembrane domain receptor using methods previously described [29]--[32](Figure 1).
(A) A CXCR4 - specific ZFN
pair was generated, comprised of two DNA - binding
zinc finger proteins (ZFPs) each fused with a FokI endonuclease monomer.
Here we describe engineering a
pair of
zinc finger nucleases that, when introduced into human T cells, efficiently disrupt cxcr4 by cleavage and error - prone non-homologous DNA end - joining.
To circumvent this, a CCR5 specific
zinc -
finger nuclease
pair (R5 - ZFNs) has been developed [23].