CRISPR-mediated multiplexed live cell imaging of nonrepetitive genomic loci with one guide RNA per locus

被引:52
作者
Clow, Patricia A. [1 ]
Du, Menghan [1 ,2 ]
Jillette, Nathaniel [1 ]
Taghbalout, Aziz [1 ]
Zhu, Jacqueline J. [1 ,3 ]
Cheng, Albert W. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Jackson Lab Genom Med, Farmington, CT 06032 USA
[2] Univ Connecticut, Dept Genet & Genome Sci, Hlth Ctr, Farmington, CT 06030 USA
[3] Arizona State Univ, Sch Biol & Hlth Syst Engn, Tempe, AZ 85281 USA
[4] Jackson Lab Canc Ctr, Bar Harbor, ME 04609 USA
[5] Univ Connecticut, Hlth Ctr, Inst Syst Genom, Farmington, CT 06030 USA
基金
美国国家科学基金会;
关键词
DNA-SEQUENCES; VISUALIZATION; TRANSCRIPTION; ORGANIZATION; PROTEINS; PLATFORM; BROWSER; RANGE;
D O I
10.1038/s41467-022-29343-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Three-dimensional (3D) structures of the genome are dynamic, heterogeneous and functionally important. Here the authors present a CRISPR-based approach for labeling the genome at multiple nonrepetitive loci in living cells and to image chromatin loops in the presence and absence of cohesin. Three-dimensional (3D) structures of the genome are dynamic, heterogeneous and functionally important. Live cell imaging has become the leading method for chromatin dynamics tracking. However, existing CRISPR- and TALE-based genomic labeling techniques have been hampered by laborious protocols and are ineffective in labeling non-repetitive sequences. Here, we report a versatile CRISPR/Casilio-based imaging method that allows for a nonrepetitive genomic locus to be labeled using one guide RNA. We construct Casilio dual-color probes to visualize the dynamic interactions of DNA elements in single live cells in the presence or absence of the cohesin subunit RAD21. Using a three-color palette, we track the dynamic 3D locations of multiple reference points along a chromatin loop. Casilio imaging reveals intercellular heterogeneity and interallelic asynchrony in chromatin interaction dynamics, underscoring the importance of studying genome structures in 4D.
引用
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页数:10
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