Cell-specific effects of the sole C. elegans Daughterless/E protein homolog, HLH-2, on nervous system development

Author:

Masoudi Neda1ORCID,Schnabel Ralf2ORCID,Yemini Eviatar13ORCID,Leyva-Díaz Eduardo1ORCID,Hobert Oliver1ORCID

Affiliation:

1. Columbia University, Howard Hughes Medical Institute 1 Department of Biological Sciences , , New York, NY 10027 , USA

2. Institute of Genetics, Technische Universität Braunschweig 2 , 38106 Braunschweig , Germany

3. University of Massachusetts 3 , Department of Neurobiology, Worcester, MA 1605-2324 , USA

Abstract

ABSTRACT Are there common mechanisms of neurogenesis used throughout an entire nervous system? We explored to what extent canonical proneural class I/II bHLH complexes are responsible for neurogenesis throughout the entire Caenorhabditis 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 Daughterless in flies, the E 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 found that hlh-2 selectively affects some aspects of neuron differentiation while leaving others unaffected. Although 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.

Funder

National Institutes of Health

Howard Hughes Medical Institute

Columbia University

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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