Multidimensional regulation of gene expression in the C. elegans embryo
- John Isaac Murray1,2,
- Thomas J. Boyle1,
- Elicia Preston1,2,
- Dionne Vafeados1,
- Barbara Mericle1,
- Peter Weisdepp1,
- Zhongying Zhao1,4,
- Zhirong Bao1,3,
- Max Boeck1 and
- Robert H. Waterston1,5
- 1Department of Genome Sciences, University of Washington School of Medicine, Seattle, Washington 98195, USA;
- 2Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA;
- 3Developmental Biology Program, Sloan-Kettering Institute for Cancer Research, New York, New York 10065, USA
Abstract
How cells adopt different expression patterns is a fundamental question of developmental biology. We quantitatively measured reporter expression of 127 genes, primarily transcription factors, in every cell and with high temporal resolution in C. elegans embryos. Embryonic cells are highly distinct in their gene expression; expression of the 127 genes studied here can distinguish nearly all pairs of cells, even between cells of the same tissue type. We observed recurrent lineage-regulated expression patterns for many genes in diverse contexts. These patterns are regulated in part by the TCF-LEF transcription factor POP-1. Other genes' reporters exhibited patterns correlated with tissue, position, and left–right asymmetry. Sequential patterns both within tissues and series of sublineages suggest regulatory pathways. Expression patterns often differ between embryonic and larval stages for the same genes, emphasizing the importance of profiling expression in different stages. This work greatly expands the number of genes in each of these categories and provides the first large-scale, digitally based, cellular resolution compendium of gene expression dynamics in live animals. The resulting data sets will be a useful resource for future research.
Footnotes
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↵5 Corresponding author
E-mail waterston{at}gs.washington.edu
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[Supplemental material is available for this article.]
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Article published online before print. Article, supplemental material, and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.131920.111.
Freely available online through the Genome Research Open Access option.
- Received September 13, 2011.
- Accepted April 5, 2012.
This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported License), as described at http://creativecommons.org/licenses/by-nc/3.0/.











