A quantitative spatiotemporal atlas of gene expression in the Drosophila blastoderm

被引:190
作者
Fowlkes, Charless C. [1 ,2 ]
Luengo Hendriks, Cris L. [1 ,3 ]
Keraenen, Soile V. E. [1 ,4 ]
Weber, Gunther H. [1 ,5 ]
Ruebel, Oliver [1 ,5 ,6 ]
Huang, Min-Yu [1 ,5 ,6 ]
Chatoor, Sohail [1 ,3 ,6 ]
DePace, Angela H. [1 ,4 ]
Simirenko, Lisa [1 ,4 ]
Henriquez, Clara [1 ,4 ]
Beaton, Amy [4 ]
Weiszmann, Richard [4 ]
Celniker, Susan [1 ,3 ]
Hamann, Bernd [1 ,5 ,6 ]
Knowles, David W. [1 ,3 ]
Biggin, Mark D. [1 ,4 ]
Eisen, Michael B. [1 ,4 ]
Malik, Jitendra [1 ,7 ]
机构
[1] Univ Calif Irvine, Berkeley Drosophila Transcript Network Project, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Comp Sci, Irvine, CA 92697 USA
[3] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Lab, Genom Div, Berkeley, CA 94720 USA
[5] Univ Calif Davis, Inst Data Anal & Visualizat IDAV, Davis, CA 95616 USA
[6] Univ Calif Davis, Dept Comp Sci, Davis, CA 95616 USA
[7] Univ Calif Berkeley, Dept Elect Engn & Comp Sci, Berkeley, CA 94720 USA
关键词
D O I
10.1016/j.cell.2008.01.053
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To fully understand animal transcription networks, it is essential to accurately measure the spatial and temporal expression patterns of transcription factors and their targets. We describe a registration technique that takes image-based data from hundreds of Drosophila blastoderm embryos, each costained for a reference gene and one of a set of genes of interest, and builds a model VirtualEmbryo. This model captures in a common framework the average expression patterns for many genes in spite of significant variation in morphology and expression between individual embryos. We establish the method's accuracy by showing that relationships between a pair of genes' expression inferred from the model are nearly identical to those measured in embryos costained for the pair. We present a VirtualEmbryo containing data for 95 genes at six time cohorts. We show that known gene-regulatory interactions can be automatically recovered from this data set and predict hundreds of new interactions.
引用
收藏
页码:364 / 374
页数:11
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