Genome-Wide Mapping of Collier In Vivo Binding Sites Highlights Its Hierarchical Position in Different Transcription Regulatory Networks
Genome-Wide Mapping of Collier In Vivo Binding Sites Highlights Its Hierarchical Position in Different Transcription Regulatory Networks
Collier, the single Drosophila COE (Collier/EBF/Olf-1) transcription factor, is required in several developmental processes, including head patterning and specification of muscle and neuron identity during embryogenesis. To identify direct Collier (Col) targets in different cell types, we used ChIP-seq to map Col binding sites throughout the genome, at mid-embryogenesis. In vivo Col binding peaks were associated to 415 potential direct target genes. Gene Ontology analysis revealed a strong enrichment in proteins with DNA binding and/or transcription-regulatory properties. Characterization of a selection of candidates, using transgenic CRM-reporter assays, identified direct Col targets in dorso-lateral somatic muscles and specific neuron types in the central nervous system. These data brought new evidence that Col direct control of the expression of the transcription regulators apterous and eyes-absent (eya) is critical to specifying neuronal identities. They also showed that cross-regulation between col and eya in muscle progenitor cells is required for specification of muscle identity, revealing a new parallel between the myogenic regulatory networks operating in Drosophila and vertebrates. Col regulation of eya, both in specific muscle and neuronal lineages, may illustrate one mechanism behind the evolutionary diversification of Col biological roles.
- University of Strasbourg France
- National Research Institute for Agriculture, Food and Environment France
- Institute of Genetics and Molecular and Cellular Biology France
- UNIVERSITE FEDERALE DE TOULOUSE MIDI-PYRENEES France
- Département Sciences sociales, agriculture et alimentation, espace et environnement France
570, Embryo, Nonmammalian, Chip-Seq data, Science, Embryonic Development, [MATH] Mathematics [math], [INFO] Computer Science [cs], Animals, Genetically Modified, DNA;B-CELL factor;Gene-expression;Functional-characterization;Chip-Seq data;Drosophila-Melanogaster;Muscle development;Enrichment analysis;Target genes;Specification, Animals, Drosophila Proteins, [INFO]Computer Science [cs], Drosophila-Melanogaster, Gene Regulatory Networks, Gene-expression, Functional-characterization, Muscle development, [MATH]Mathematics [math], Body Patterning, Enrichment analysis, Binding Sites, Q, R, Chromosome Mapping, Gene Expression Regulation, Developmental, DNA, Drosophila melanogaster, B-CELL factor, Medicine, Target genes, Specification, Research Article, Signal Transduction, Transcription Factors
570, Embryo, Nonmammalian, Chip-Seq data, Science, Embryonic Development, [MATH] Mathematics [math], [INFO] Computer Science [cs], Animals, Genetically Modified, DNA;B-CELL factor;Gene-expression;Functional-characterization;Chip-Seq data;Drosophila-Melanogaster;Muscle development;Enrichment analysis;Target genes;Specification, Animals, Drosophila Proteins, [INFO]Computer Science [cs], Drosophila-Melanogaster, Gene Regulatory Networks, Gene-expression, Functional-characterization, Muscle development, [MATH]Mathematics [math], Body Patterning, Enrichment analysis, Binding Sites, Q, R, Chromosome Mapping, Gene Expression Regulation, Developmental, DNA, Drosophila melanogaster, B-CELL factor, Medicine, Target genes, Specification, Research Article, Signal Transduction, Transcription Factors
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