Castaño Julio, Bueno Clara, Jiménez-Delgado Senda, Roca-Ho Heleia, Fraga Mario F, Fernandez Agustín F, Nakanishi Mahito, Torres-Ruiz Raúl, Rodríguez-Perales Sandra, Menéndez Pablo
Josep Carreras Leukemia Research Institute, Department of Biomedicine, School of Medicine, University of Barcelona, Barcelona, Spain; Center for Networked Biomedical Research on Cancer (CIBERONC), ISCIII, Madrid, Spain.
Josep Carreras Leukemia Research Institute, Department of Biomedicine, School of Medicine, University of Barcelona, Barcelona, Spain; Center for Networked Biomedical Research on Cancer (CIBERONC), ISCIII, Madrid, Spain.
Stem Cell Res. 2017 May;21:137-140. doi: 10.1016/j.scr.2017.04.011. Epub 2017 Apr 22.
We report the generation-characterization of a fetal liver (FL) B-cell progenitor (BCP)-derived human induced pluripotent stem cell (hiPSC) line CRISPR/Cas9-edited to carry/express a single copy of doxycycline-inducible Cas9 gene in the "safe locus" AAVS1 (iCas9-FL-BCP-hiPSC). Gene-edited iPSCs remained pluripotent after CRISPR/Cas9 genome-edition. Correct genomic integration of a unique copy of Cas9 was confirmed by PCR and Southern blot. Cas9 was robustly and specifically expressed on doxycycline exposure. T7-endonuclease assay demonstrated that iCas9 induces robust gene-edition when gRNAs against hematopoietic transcription factors were tested. This iCas9-FL-BCP-hiPSC will facilitate gene-editing approaches for studies on developmental biology, drug screening and disease modeling.
我们报告了一种源自胎儿肝脏(FL)B细胞祖细胞(BCP)的人类诱导多能干细胞(hiPSC)系的生成与表征,该细胞系经CRISPR/Cas9编辑,在“安全位点”AAVS1中携带/表达单拷贝强力霉素诱导型Cas9基因(iCas9-FL-BCP-hiPSC)。经CRISPR/Cas9基因组编辑后,基因编辑的iPSC仍保持多能性。通过PCR和Southern印迹证实了Cas9单拷贝的正确基因组整合。在暴露于强力霉素时,Cas9得到了强有力且特异性的表达。当测试针对造血转录因子的gRNA时,T7核酸内切酶测定表明iCas9可诱导强有力的基因编辑。这种iCas9-FL-BCP-hiPSC将促进用于发育生物学、药物筛选和疾病建模研究的基因编辑方法。