Quantitative approaches for investigating the spatial context of gene expression

被引:25
|
作者
Lee, Je H. [1 ]
机构
[1] Cold Spring Harbor Lab, POB 100, Cold Spring Harbor, NY 11724 USA
关键词
CELL RNA-SEQ; IN-SITU; POSITIONAL INFORMATION; SINGLE CELLS; STEM-CELLS; GENOME; TISSUE; PROBES; AMPLIFICATION; METASTASIS;
D O I
10.1002/wsbm.1369
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The spatial information associated with gene expression is important for elucidating the context-dependent transcriptional regulation during development. Recently, high-resolution sampling approaches, such as RNA tomography or single-cell RNA-seq combined with fluorescence in situ hybridization (FISH), have provided indirect ways to view global gene expression patterns in three dimensions. Now in situ sequencing technologies, such as fluorescent in situ sequencing (FISSEQ), are attempting to visualize the genetic signature directly in microscope images. This article will examine the basic principle of modern in situ and single-cell genetic methods, hurdles in quantifying intrinsic and extrinsic forces that influence cell decision-making, and technological requirements for making a visual map of gene regulation, form, and function. Successfully addressing these challenges will be essential for investigating the functional evolution of regulatory sequences during growth, development, and cancer progression. (C) 2016 The Authors. WIREs Systems Biology and Medicine published by Wiley Periodicals, Inc.
引用
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页数:13
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