دورية أكاديمية
Targeted Repair of CYBB in X-CGD iPSCs Requires Retention of Intronic Sequences for Expression and Functional Correction.
| العنوان: | Targeted Repair of CYBB in X-CGD iPSCs Requires Retention of Intronic Sequences for Expression and Functional Correction. |
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| المؤلفون: | Sweeney, Colin L, Zou, Jizhong, Choi, Uimook, Merling, Randall K, Liu, Alexander, Bodansky, Aaron, Burkett, Sandra, Kim, Jung-Woong, De Ravin, Suk See, Malech, Harry L |
| المصدر: | Mol Ther ; ISSN:1525-0024 ; Volume:25 ; Issue:2 |
| بيانات النشر: | Elsevier Science |
| سنة النشر: | 2017 |
| المجموعة: | PubMed Central (PMC) |
| مصطلحات موضوعية: | CRISPR, TALEN, X-linked chronic granulomatous disease, iPSC, intron, targeted correction |
| الوصف: | X-linked chronic granulomatous disease (X-CGD) is an immune deficiency resulting from defective production of microbicidal reactive oxygen species (ROS) by phagocytes. Causative mutations occur throughout the CYBB gene, resulting in absent or defective gp91phox protein expression. To correct CYBB exon 5 mutations while retaining normal gene regulation, we utilized TALEN or Cas9 for exon 5 replacement in induced pluripotent stem cells (iPSCs) from patients, which restored gp91phox expression and ROS production in iPSC-derived granulocytes. Alternate approaches for correcting the majority of X-CGD mutations were assessed, involving TALEN- or Cas9-mediated insertion of CYBB minigenes at exon 1 or 2 of the CYBB locus. Targeted insertion of an exon 1-13 minigene into CYBB exon 1 resulted in no detectable gp91phox expression or ROS activity in iPSC-derived granulocytes. In contrast, targeted insertion of an exon 2-13 minigene into exon 2 restored both gp91phox and ROS activity. This demonstrates the efficacy of two correction strategies: seamless repair of specific CYBB mutations by exon replacement or targeted insertion of an exon 2-13 minigene to CYBB exon 2 while retaining exon/intron 1. Furthermore, it highlights a key issue for targeted insertion strategies for expression from an endogenous promoter: retention of intronic elements can be necessary for expression. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| العلاقة: | https://doi.org/10.1016/j.ymthe.2016.11.012Test; https://pubmed.ncbi.nlm.nih.gov/28153086Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368476Test/ |
| DOI: | 10.1016/j.ymthe.2016.11.012 |
| الإتاحة: | https://doi.org/10.1016/j.ymthe.2016.11.012Test https://pubmed.ncbi.nlm.nih.gov/28153086Test https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368476Test/ |
| حقوق: | Published by Elsevier Inc. |
| رقم الانضمام: | edsbas.68F818 |
| قاعدة البيانات: | BASE |
| DOI: | 10.1016/j.ymthe.2016.11.012 |
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