DevelopmentNeurosciencePeer-reviewed journal article
Restricted effects of the sole C. elegans Daughterless/E homolog, HLH-2, on nervous system development
Neda MasoudiiD, Ralf SchnabeliD, Eviatar YeminiiD, Eduardo Leyva‐DíaziD, Oliver HobertiD
Abstract
Are there common mechanisms of neurogenesis used throughout an entire nervous system? Making use of the well-defined and relatively small size of the nervous system of the nematode C. elegans, we explored to what extent canonical proneural class I/II bHLH complexes are responsible for neurogenesis throughout the entire C. elegans nervous system. Distinct, lineage-specific proneural "class II" bHLH factors are generally thought to operate via interaction with a common, "class I" bHLH subunit, encoded by Daugtherless in flies, the E (E2A, E2-2, HEB) proteins in vertebrates, and hlh-2 in C. elegans. To eliminate function of all proneuronal class I/II bHLH complexes, we therefore genetically removed maternal and zygotic hlh-2 gene activity. We observed broad effects on neurogenesis, but still detected normal neurogenesis in many distinct neuron-producing lineages of the central and peripheral nervous system. Moreover, we find that hlh-2 selectively affects some aspects of neuron differentiation while leaving others unaffected. While our studies confirm the function of proneuronal class I/II bHLH complexes in many different lineages throughout a nervous system, we conclude that their function is not universal, but rather restricted by lineage, cell type and components of differentiation programs affected.
- organism: C. elegans
- research focus: cell type annotation
- research focus: differential expression
- research focus: gene regulatory network inference
- research focus: cell-cell communication
- approach: experimental assay
- Citations
- 3
- FWCI
- 0.27
- Field percentile
- 41th percentile
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