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Generation and characterization of the human iPSC line CABi001-A from a patient with retinitis pigmentosa caused by a novel mutation in PRPF31 gene

AuthorsCerda, Berta de la ; Díez-Lloret, Andrea ; Ponte-Zuñiga, Beatriz; Vallés-Saiz, Laura; Calado, Sofia M.; Rodriguez-Bocanegra, Eduardo; García-Delgado, Ana B.; Moya-Molina, Marina; Bhattacharya, Shom Shanker ; Díaz-Corrales, Francisco J.
Issue DateApr-2019
PublisherElsevier BV
CitationStem Cell Research 36: 101426 (2019)
AbstractPRPF31 gene codes for a ubiquitously expressed splicing factor but mutations affect exclusively the retina, producing the progressive death of photoreceptor cells. We have identified a novel PRPF31 mutation in a patient with autosomal dominant retinitis pigmentosa. A blood sample was obtained and mononuclear cells were reprogrammed using the non-integrative Sendai virus to generate the cell line CABi001-A. The iPSC line has been characterized for pluripotency and differentiation capacity and will be differentiated toward photoreceptors and retinal pigment epithelium cells to study the molecular mechanism of the disease and test possible therapeutic strategies.
Publisher version (URL)http://dx.doi.org/10.1016/j.scr.2019.101426
Identifiersdoi: 10.1016/j.scr.2019.101426
e-issn: 1876-7753
issn: 1873-5061
Appears in Collections:(CABIMER) Artículos
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