清脆的
核酸
基因组编辑
生物
Cas9
DNA
基因组
计算生物学
遗传学
抄写(语言学)
基因
核糖核酸
细胞生物学
分子生物学
语言学
哲学
作者
Haifeng Wang,Muneaki Nakamura,Timothy R. Abbott,Dehua Zhao,Kaiwen Luo,Cordelia Yu,Cindy M. Nguyen,Albert Lo,Timothy Daley,Marie La Russa,Yanxia Liu,Lei S. Qi
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2019-09-05
卷期号:365 (6459): 1301-1305
被引量:229
标识
DOI:10.1126/science.aax7852
摘要
We report a robust, versatile approach called CRISPR live-cell fluorescent in situ hybridization (LiveFISH) using fluorescent oligonucleotides for genome tracking in a broad range of cell types, including primary cells. An intrinsic stability switch of CRISPR guide RNAs enables LiveFISH to accurately detect chromosomal disorders such as Patau syndrome in prenatal amniotic fluid cells and track multiple loci in human T lymphocytes. In addition, LiveFISH tracks the real-time movement of DNA double-strand breaks induced by CRISPR-Cas9-mediated editing and consequent chromosome translocations. Finally, by combining Cas9 and Cas13 systems, LiveFISH allows for simultaneous visualization of genomic DNA and RNA transcripts in living cells. The LiveFISH approach enables real-time live imaging of DNA and RNA during genome editing, transcription, and rearrangements in single cells.
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