High-resolution, three-dimensional mapping of gene expression using GeneExpressMap (GEM)

被引:5
作者
Flynn, C. J. [1 ,2 ]
Sharma, T. [1 ]
Ruffins, S. W. [3 ]
Guerra, S. L. [1 ]
Crowley, J. C. [1 ,2 ]
Ettensohn, C. A. [1 ]
机构
[1] Carnegie Mellon Univ, Dept Biol Sci, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Ctr Neural Basis Cognit, Pittsburgh, PA 15213 USA
[3] CALTECH, Biol Imaging Ctr, Pasadena, CA 91125 USA
基金
美国国家科学基金会;
关键词
Gene expression; Multiplex fluorescent in situ hybridization; Gene regulatory network; Sea urchin; GeneExpressMap; GEM; Image processing; SEA-URCHIN EMBRYO; PRIMARY MESENCHYME CELLS; REGULATORY NETWORKS; SPECIFICATION; ETS; HYBRIDIZATION; ENDOMESODERM; INGRESSION; PLASTICITY; EVOLUTION;
D O I
10.1016/j.ydbio.2011.06.033
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The analysis of temporal and spatial patterns of gene expression is critically important for many kinds of developmental studies, including the construction of gene regulatory networks. Recently, multiplex, fluorescent, whole mount in situ hybridization (multiplex F-WMISH), applied in combination with confocal microscopy, has emerged as the method of choice for high-resolution, three-dimensional (3D) mapping of gene expression patterns in developing tissues. We have developed an image analysis tool, GeneExpressMap (GEM), that facilitates the rapid, 3D analysis of multiplex F-WMISH data at single-cell resolution. GEM assigns F-WMISH signal to individual cells based upon the proximity of cytoplasmic hybridization signal to cell nuclei. Here, we describe the features of GEM and, as a test of its utility, we use GEM to analyze patterns of regulatory gene expression in the non-skeletogenic mesoderm of the early sea urchin embryo. GEM greatly extends the power of multiplex F-WMISH for analyzing patterns of gene expression and is a valuable tool for gene network analysis and many other kinds of developmental studies. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:532 / 540
页数:9
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