Highly efficient and robust π-FISH rainbow for multiplexed in situ detection of diverse biomolecules.
Yingfeng TaoXiaoliu ZhouLeqiang SunDa LinHuaiyuan CaiXi ChenWei ZhouBing YangZhe HuJing YuJing ZhangXiaoqing YangFang YangBang ShenWenbao QiZhenfang FuJinxia DaiGang CaoPublished in: Nature communications (2023)
In the unprecedented single-cell sequencing and spatial multiomics era of biology, fluorescence in situ hybridization (FISH) technologies with higher sensitivity and robustness, especially for detecting short RNAs and other biomolecules, are greatly desired. Here, we develop the robust multiplex π-FISH rainbow method to detect diverse biomolecules (DNA, RNA, proteins, and neurotransmitters) individually or simultaneously with high efficiency. This versatile method is successfully applied to detect gene expression in different species, from microorganisms to plants and animals. Furthermore, we delineate the landscape of diverse neuron subclusters by decoding the spatial distribution of 21 marker genes via only two rounds of hybridization. Significantly, we combine π-FISH rainbow with hybridization chain reaction to develop π-FISH+ technology for short nucleic acid fragments, such as microRNA and prostate cancer anti-androgen therapy-resistant marker ARV7 splicing variant in circulating tumour cells from patients. Our study provides a robust biomolecule in situ detection technology for spatial multiomics investigation and clinical diagnosis.
Keyphrases
- nucleic acid
- single cell
- prostate cancer
- highly efficient
- gene expression
- single molecule
- high efficiency
- label free
- rna seq
- real time pcr
- high throughput
- end stage renal disease
- ejection fraction
- dna methylation
- newly diagnosed
- chronic kidney disease
- loop mediated isothermal amplification
- radical prostatectomy
- bone marrow
- circulating tumor
- mesenchymal stem cells