Real-time single-molecule imaging of transcriptional regulatory networks in living cells

被引:10
|
作者
Hwang, Dong-Woo [1 ]
Maekiniemi, Anna [1 ]
Singer, Robert H. [1 ]
Sato, Hanae [1 ,2 ]
机构
[1] Albert Einstein Coll Med, Dept Cell Biol, New York, NY 10033 USA
[2] Kanazawa Univ, WPI Nano Life Sci Inst WPI Nano LSI, Kakuma Machi, Kanazawa 9201192, Japan
关键词
FLUORESCENCE CORRELATION SPECTROSCOPY; DECAY PRODUCTS IMPLICATIONS; ASH1; MESSENGER-RNA; GENE-EXPRESSION; HISTONE MODIFICATIONS; PRC2; RECRUITMENT; STRUCTURAL BASIS; 3' DEGRADATION; LIVE CELLS; BLOCK 5';
D O I
10.1038/s41576-023-00684-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Gene regulatory networks drive the specific transcriptional programmes responsible for the diversification of cell types during the development of multicellular organisms. Although our knowledge of the genes involved in these dynamic networks has expanded rapidly, our understanding of how transcription is spatiotemporally regulated at the molecular level over a wide range of timescales in the small volume of the nucleus remains limited. Over the past few decades, advances in the field of single-molecule fluorescence imaging have enabled real-time behaviours of individual transcriptional components to be measured in living cells and organisms. These efforts are now shedding light on the dynamic mechanisms of transcription, revealing not only the temporal rules but also the spatial coordination of underlying molecular interactions during various biological events. In this Review, Hwang and co-authors outline single-molecule fluorescence imaging techniques that can be used in living cells to visualize individual molecules involved in the spatiotemporal regulation of gene expression. This Review also delves into the biological insights gained through these methodologies.
引用
收藏
页码:272 / 285
页数:14
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