Spatially resolved, highly multiplexed RNA profiling in single cells

被引:1743
作者
Chen, Kok Hao [1 ]
Boettiger, Alistair N. [1 ]
Moffitt, Jeffrey R. [1 ]
Wang, Siyuan [1 ]
Zhuang, Xiaowei [1 ,2 ]
机构
[1] Harvard Univ, Howard Hughes Med Inst, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Dept Phys, Cambridge, MA 02138 USA
基金
美国国家卫生研究院;
关键词
GENE-EXPRESSION; MOLECULE FLUORESCENCE; MESSENGER-RNAS; DESIGN; VISUALIZATION; TRANSLOCATION; LOCALIZATION; MECHANISMS; REVEALS; TOOL;
D O I
10.1126/science.aaa6090
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
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Knowledge of the expression profile and spatial landscape of the transcriptome in individual cells is essential for understanding the rich repertoire of cellular behaviors. Here, we report multiplexed error-robust fluorescence in situ hybridization (MERFISH), a single-molecule imaging approach that allows the copy numbers and spatial localizations of thousands of RNA species to be determined in single cells. Using error-robust encoding schemes to combat single-molecule labeling and detection errors, we demonstrated the imaging of 100 to 1000 distinct RNA species in hundreds of individual cells. Correlation analysis of the similar to 10(4) to 10(6) pairs of genes allowed us to constrain gene regulatory networks, predict novel functions for many unannotated genes, and identify distinct spatial distribution patterns of RNAs that correlate with properties of the encoded proteins.
引用
收藏
页数:15
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