Advancing towards a global mammalian gene regulation model through single-cell analysis and synthetic biology

被引:7
|
作者
Tycko, Josh [1 ]
Van, Mike V. [2 ]
Elowitz, Michael B. [3 ,4 ]
Bintu, Lacramioara [5 ]
机构
[1] Stanford Univ, Dept Genet, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
[3] CALTECH, Div Biol & Biol Engn, Pasadena, CA 91125 USA
[4] CALTECH, Howard Hughes Med Inst HHMI, Dept Appl Phys, Pasadena, CA 91125 USA
[5] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
关键词
Gene regulation; Chromatin; Single-cell; Modelling; Synthetic biology;
D O I
10.1016/j.cobme.2017.10.011
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Engineering complex genetic functions in mammalian cells will require predictive models of gene regulation. Since gene expression is stochastic, leading to cell-to-cell heterogeneity, these models depend on single-cell measurements. Here, we summarize recent microscopy and sequencing-based single-cell measurements of transcription and its chromatin-based regulation. Then, we describe synthetic biology methods for manipulating chromatin, and highlight how they could be coupled to single-cell measurements. We discuss theoretical models that connect some chromatin inputs to transcriptional outputs. Finally, we point out the connections between the models that would allow us to integrate them into one global input-output gene regulatory function.
引用
收藏
页码:174 / 193
页数:20
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