Engineering inducible biomolecular assemblies for genome imaging and manipulation in living cells.
Qin PengZiliang HuangKun SunYahan LiuChi Woo YoonReed E S HarrisonDanielle L SchmittLinshan ZhuYiqian WuIpek TasanHuimin ZhaoJin ZhangSheng ZhongShu ChienYingxiao WangPublished in: Nature communications (2022)
Genome architecture and organization play critical roles in cell life. However, it remains largely unknown how genomic loci are dynamically coordinated to regulate gene expression and determine cell fate at the single cell level. We have developed an inducible system which allows Simultaneous Imaging and Manipulation of genomic loci by Biomolecular Assemblies (SIMBA) in living cells. In SIMBA, the human heterochromatin protein 1α (HP1α) is fused to mCherry and FRB, which can be induced to form biomolecular assemblies (BAs) with FKBP-scFv, guided to specific genomic loci by a nuclease-defective Cas9 (dCas9) or a transcriptional factor (TF) carrying tandem repeats of SunTag. The induced BAs can not only enhance the imaging signals at target genomic loci using a single sgRNA, either at repetitive or non-repetitive sequences, but also recruit epigenetic modulators such as histone methyltransferase SUV39H1 to locally repress transcription. As such, SIMBA can be applied to simultaneously visualize and manipulate, in principle, any genomic locus with controllable timing in living cells.
Keyphrases
- living cells
- fluorescent probe
- genome wide
- copy number
- dna methylation
- gene expression
- genome wide association study
- single molecule
- single cell
- high resolution
- endothelial cells
- high glucose
- cell fate
- genome wide association
- diabetic rats
- high frequency
- small molecule
- transcription factor
- rna seq
- high throughput
- stem cells
- bone marrow
- cell therapy
- pluripotent stem cells
- mesenchymal stem cells
- genome editing
- fluorescence imaging