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Targeted Repair of p47-CGD in iPSCs by CRISPR/Cas9

Functional Correction without Cleavage in the Highly Homologous Pseudogenes
 
: Klatt, Denise; Cheng, Erica; Philipp, Friederike; Selich, Anton; Dahlke, Julia; Schmidt, Reinhold E.; Schott, Juliane W.; Büning, Hildegard; Hoffmann, Dirk; Thrasher, Adrian J.; Schambach, Axel

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Volltext urn:nbn:de:0011-n-5648533 (2.8 MByte PDF)
MD5 Fingerprint: a145c1e2114b9a7205f7d3793614b155
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Erstellt am: 6.12.2019


Stem cell reports 13 (2019), Nr.4, S.590-598
ISSN: 2213-6711
Englisch
Zeitschriftenaufsatz, Elektronische Publikation
Fraunhofer ITEM ()
chronic granulomatous disease (CGD); NADPH oxidase; p47phox; NCF1; CRISPR / Cas9; human induced pluripotent stem cells; gene editing; Pseudogenes

Abstract
Mutations in the NADPH oxidase, which is crucial for the respiratory burst in phagocytes, result in chronic granulomatous disease (CGD). The only curative treatment option for CGD patients, who suffer from severe infections, is allogeneic bone marrow transplantation. Over 90% of patients with mutations in the p47phox subunit of the oxidase complex carry the deletion c.75 76delGT (ΔGT). This frequent mutation most likely originates via gene conversion from one of the two pseudogenes NCF1B or NCF1C, which are highly homologous to NCF1 (encodes p47phox) but carry the ΔGT mutation. We applied CRISPR/Cas9 to generate patient-like p47-ΔGT iPSCs for disease modeling. To avoid unpredictable chromosomal rearrangements by CRISPR/Cas9-mediated cleavage in the pseudogenes, we developed a gene-correction approach to specifically target NCF1 but leave the pseudogenes intact. Functional assays revealed restored NADPH oxidase activity and killing of bacteria in corrected phagocytes as well as the specificity of this approach.

: http://publica.fraunhofer.de/dokumente/N-564853.html