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Genome-Wide Mapping of Collier In Vivo Binding Sites Highlights Its Hierarchical Position in Different Transcription
Mathilde de Taffin1, Yannick Carrier1, Laurence Dubois1
1Centre de Biologie du Développement, UMR 5547 CNRS Université de Toulouse 3, 118 route de Narbonne, F-31062, Toulouse cedex 09, France.
Abstract:
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.
Insights
Collier (Col) transcription factor directly regulates genes essential for muscle and neuron development in Drosophila embryos. This study identifies direct Col targets, revealing its critical role in specifying cell identities and evolutionary conserved regulatory networks.
Area of Science:
- Developmental Biology
- Genetics
- Molecular Biology
Background:
- The Drosophila transcription factor Collier (Col) is crucial for embryonic development, including head patterning and cell identity specification.
- Understanding direct Col targets is key to elucidating its regulatory mechanisms in different cell types.
Purpose of the Study:
- To identify direct Collier (Col) target genes genome-wide using ChIP-seq.
- To investigate the role of Col in specifying muscle and neuronal identities during embryogenesis.
Main Methods:
- Chromatin immunoprecipitation followed by sequencing (ChIP-seq) to map Col binding sites.
- Gene Ontology analysis to identify functions of target genes.
- Transgenic reporter assays to validate direct Col targets and regulatory interactions.
Main Results:
- ChIP-seq identified 415 potential direct Col target genes.
- Target genes are enriched for DNA binding and transcription regulatory functions.
- Direct Col targets were confirmed in somatic muscles and central nervous system neurons.
- Col regulates apterous and eyes absent (eya) for neuronal identity and muscle progenitor specification.
Conclusions:
- Col directly controls key transcription regulators, including apterous and eyes-absent (eya), essential for neuronal and muscle identity.
- Cross-regulation between Col and eya in muscle progenitors highlights conserved myogenic regulatory networks.
- Col's regulation of eya in distinct lineages may explain its diverse biological roles and evolutionary diversification.
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