| Literature DB >> 30890567 |
Julia P Brandt1, Mary Rossillo1, Zhuo Du2, David Ichikawa3, Kristopher Barnes2, Allison Chen2, Marcus Noyes3, Zhirong Bao2, Niels Ringstad4.
Abstract
The sensory nervous system of C. elegans comprises cells with varied molecular and functional characteristics, and is, therefore, a powerful model for understanding mechanisms that generate neuronal diversity. We report here that VAB-3, a C. elegans homolog of the homeodomain-containing protein Pax6, has opposing functions in regulating expression of a specific chemosensory fate. A homeodomain-only short isoform of VAB-3 is expressed in BAG chemosensory neurons, where it promotes gene expression and cell function. In other cells, a long isoform of VAB-3, comprising a Paired homology domain and a homeodomain, represses expression of ETS-5, a transcription factor required for expression of BAG fate. Repression of ets-5 requires the Eyes Absent homolog EYA-1 and the Six-class homeodomain protein CEH-32. We determined sequences that mediate high-affinity binding of ETS-5, VAB-3 and CEH-32. The ets-5 locus is enriched for ETS-5-binding sites but lacks sequences that bind VAB-3 and CEH-32, suggesting that these factors do not directly repress ets-5 expression. We propose that a promoter-selection system together with lineage-specific expression of accessory factors allows VAB-3/Pax6 to either promote or repress expression of specific cell fates in a context-dependent manner. This article has an associated 'The people behind the papers' interview.Entities:
Keywords: C. elegans; Chemosensory; Nervous system; VAB-3
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Year: 2019 PMID: 30890567 PMCID: PMC6503985 DOI: 10.1242/dev.168153
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868