Previous and current research
How genomic information determines the formation of an organism is a major challenge of biology in the post-genomic era. The restriction of gene activity to subsets of cells during development leads to morphological and physiological specialization allowing the formation of tissues and organs. Although many mechanisms play a role, regulation of transcription is a primary cause of tissue specific gene expression. Our understanding paints a picture of transcriptional regulation as a complex interplay of cis-regulatory sequence elements interacting with trans-acting proteins. Combining an understanding of transcriptional regulation together with a complete genome sequence may ultimately allow a description of a developing organism as a network of interacting genetic and protein components. However, before we can begin to attempt to decipher the developmental puzzle it is essential to assemble spatio-temporal gene expression data on genome-wide scale.
It is arguable that the knowledge of the precise spatial and temporal specificity of gene expression is the necessary prerequisite for understanding gene function in animal development. The availability of complete genome sequences allows us to determine patterns of gene expression systematically for all genes in the genome using the universal RNA in situ hybridization technique. We focus on the complex, well-understood and technically accessible process of Drosophila embryogenesis and aim to create the first complete atlas of spatio-temporal expression patterns in development. The process of capturing spatial gene expression data on a genome-wide scale requires combination of seemingly unrelated disciplines of embryology and bioinformatics. Currently the patterns of gene expression are documented by digital microscopy images of whole mount embryos stained with RNA probes specific for individual genes. The images are annotated with controlled vocabularies that represent our current knowledge of the embryo anatomy. The dataset of more then 75,000 annotated embryo images representing about 50% of Drosophila genes provides solid observational foundation for the analysis of the relationship between the genome sequence, tissue specific gene expression and animal development (http://www.fruitfly.org/cgi-bin/ex/insitu.pl).
The complete atlas of patterns of gene expression will ultimately contain data for all transcripts generated from the Drosophila genome. We are expanding the scope of the project to include individual alternative transcripts, computational and micro-array based gene predictions and non-coding RNA genes. In order to increase the resolution of pattern determination we employ multiplex high-throughput fluorescent RNA in situ to visualize precise overlap of expression domains of genes with related expression patterns. In the future we intend to gradually move from capturing tissue specificity in fixed embryos towards recording the expression patterns in four-dimensions on live specimens. As a first step towards this goal we will establish a 3D model of the Drosophila embryo using the tissue specific markers identified in the course of this work.
We are also interested in studying the evolution of gene expression regulation on both the micro and macro-evolutionary scale. Systematic survey of gene expression patterns of orthologous genes in closely related species of Drosophila revealed relatively high occurrence of significant differences in developmental gene expression. By combining the powerful Drosophila experimental toolkit with comparative sequence analysis we can identify sequence determinants of the observed expression changes and explain their evolutionary origin. Finally, image based gene expression resources similar to ours are generated for many other developmental model systems. The emerging challenge is to integrate these diverse datasets into a centralized database that will allow comprehensive studies of the roles of gene expression regulation in animal development across the tree of life.

Sampling of patterns of gene expression in Drosophila embryogenesis.
Future prospects and goals
Study the evolution of cis-regulatory code by comparing patterns of gene expression in related Drosophila species
Develop imaging techniques for high throughput 4D recording of patterns of gene expression in Drosophila embryogenesis
Integrate image based gene expression resources into a cross-species evo-devo database - ImageBank
Selected publications
Tomancak P., Lai E. C., Williams R.W., Rubin G. M. (2003): Computational identification of Drosophila microRNA genes. Genome Biol. 4(7):R42
Tomancak P., Beaton A., Weiszmann R., Kwan E., Shu S., Lewis S. E., Richards S., Ashburner M., Hartenstein V., Celniker S. E., Rubin G. M. (2002): Systematic determination of patterns of gene expression during Drosophila embryogenesis. Genome Biol. 3(12):R88
Tomancak, P., Piano, F., Riechmann, V., Gunsalus, K. C., Kemphues, K. J., Ephrussi, A. (2000): A Drosophila melanogaster homologue of Caenorhabditis elegans par-1 acts at an early step in embryonic-axis formation. Nat Cell Biol. 2(7), 458-60.
Tomancak, P., Guichet, A., Zavorsky, P., Ephrussi, A. (1998): Oocyte polarity depends on regulation of gurken by Vasa. Development 125, 1723-1732.
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Pavel Tomancak
1995-1999: PhD work at EMBL Heidelberg, Germany
2000-2004: Postdoctoral work at the Dept. of Molecular and Cell Biology, University of California in Berkeley
since 2005: Group leader at the Max-Planck-Institute of Molecular Cell Biology and Genetics, Dresden, Germany
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