Differential gene regulation in DAPT-treated Hydra reveals candidate direct Notch signalling targets

ABSTRACT In Hydra, Notch inhibition causes defects in head patterning and prevents differentiation of proliferating nematocyte progenitor cells into mature nematocytes. To understand the molecular mechanisms by which the Notch pathway regulates these processes, we performed RNA-seq and identified ge...

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Published inJournal of cell science Vol. 134; no. 15
Main Authors Moneer, Jasmin, Siebert, Stefan, Krebs, Stefan, Cazet, Jack, Prexl, Andrea, Pan, Qin, Juliano, Celina, Böttger, Angelika
Format Journal Article
LanguageEnglish
Published The Company of Biologists Ltd 01.08.2021
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Summary:ABSTRACT In Hydra, Notch inhibition causes defects in head patterning and prevents differentiation of proliferating nematocyte progenitor cells into mature nematocytes. To understand the molecular mechanisms by which the Notch pathway regulates these processes, we performed RNA-seq and identified genes that are differentially regulated in response to 48 h of treating the animals with the Notch inhibitor DAPT. To identify candidate direct regulators of Notch signalling, we profiled gene expression changes that occur during subsequent restoration of Notch activity and performed promoter analyses to identify RBPJ transcription factor-binding sites in the regulatory regions of Notch-responsive genes. Interrogating the available single-cell sequencing data set revealed the gene expression patterns of Notch-regulated Hydra genes. Through these analyses, a comprehensive picture of the molecular pathways regulated by Notch signalling in head patterning and in interstitial cell differentiation in Hydra emerged. As prime candidates for direct Notch target genes, in addition to Hydra (Hy)Hes, we suggest Sp5 and HyAlx. They rapidly recovered their expression levels after DAPT removal and possess Notch-responsive RBPJ transcription factor-binding sites in their regulatory regions.
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Handling Editor: John Heath
ISSN:0021-9533
1477-9137
DOI:10.1242/jcs.258768