Regulatory Pathway Analysis by High-Throughput In Situ Hybridization
pmid: 17953485
pmc: PMC2041993
Regulatory Pathway Analysis by High-Throughput In Situ Hybridization
Automated in situ hybridization enables the construction of comprehensive atlases of gene expression patterns in mammals. Such atlases can become Web-searchable digital expression maps of individual genes and thus offer an entryway to elucidate genetic interactions and signaling pathways. Towards this end, an atlas housing approximately 1,000 spatial gene expression patterns of the midgestation mouse embryo was generated. Patterns were textually annotated using a controlled vocabulary comprising >90 anatomical features. Hierarchical clustering of annotations was carried out using distance scores calculated from the similarity between pairs of patterns across all anatomical structures. This process ordered hundreds of complex expression patterns into a matrix that reflects the embryonic architecture and the relatedness of patterns of expression. Clustering yielded 12 distinct groups of expression patterns. Because of the similarity of expression patterns within a group, members of each group may be components of regulatory cascades. We focused on the group containing Pax6, an evolutionary conserved transcriptional master mediator of development. Seventeen of the 82 genes in this group showed a change of expression in the developing neocortex of Pax6-deficient embryos. Electromobility shift assays were used to test for the presence of Pax6-paired domain binding sites. This led to the identification of 12 genes not previously known as potential targets of Pax6 regulation. These findings suggest that cluster analysis of annotated gene expression patterns obtained by automated in situ hybridization is a novel approach for identifying components of signaling cascades.
- Max Planck Society Germany
- Max Planck Institute for Biophysical Chemistry Germany
- Baylor College of Medicine United States
- Lawrence Berkeley National Laboratory United States
- Genomics Division Lawrence Berkeley National Laboratory United States
Homeodomain Proteins, Binding Sites, Time Factors, Models, Genetic, PAX6 Transcription Factor, Gene Expression Profiling, DNA, QH426-470, Mice, Inbred C57BL, Repressor Proteins, Mice, Gene Expression Regulation, Genetic Techniques, Mice, Inbred DBA, Genetics, Animals, Cluster Analysis, Paired Box Transcription Factors, Eye Proteins, In Situ Hybridization, Research Article, Oligonucleotide Array Sequence Analysis
Homeodomain Proteins, Binding Sites, Time Factors, Models, Genetic, PAX6 Transcription Factor, Gene Expression Profiling, DNA, QH426-470, Mice, Inbred C57BL, Repressor Proteins, Mice, Gene Expression Regulation, Genetic Techniques, Mice, Inbred DBA, Genetics, Animals, Cluster Analysis, Paired Box Transcription Factors, Eye Proteins, In Situ Hybridization, Research Article, Oligonucleotide Array Sequence Analysis
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