Glycogen synthase kinase 3 has a proapoptotic function in Hydra gametogenesis

In an approach to study the evolutionary conservation of molecules of the Wnt signal transduction pathway, we analyzed the function of the major negative regulator of this pathway, GSK3 (glycogen synthase kinase 3), in the basal metazoan Hydra. Microinjection assays reveal that HyGSK3 inhibits β-cat...

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Hauptverfasser: Rentzsch, Fabian (VerfasserIn) , Holstein, Thomas W. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 1 February 2005
In: Developmental biology
Year: 2005, Jahrgang: 278, Heft: 1, Pages: 1-12
ISSN:1095-564X
DOI:10.1016/j.ydbio.2004.10.007
Online-Zugang:Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1016/j.ydbio.2004.10.007
Verlag, kostenfrei, Volltext: http://www.sciencedirect.com/science/article/pii/S0012160604007407
Volltext
Verfasserangaben:Fabian Rentzsch, Bert Hobmayer, Thomas W. Holstein
Beschreibung
Zusammenfassung:In an approach to study the evolutionary conservation of molecules of the Wnt signal transduction pathway, we analyzed the function of the major negative regulator of this pathway, GSK3 (glycogen synthase kinase 3), in the basal metazoan Hydra. Microinjection assays reveal that HyGSK3 inhibits β-catenin in zebrafish embryos, indicating that the function of GSK3 in the canonical Wnt signaling pathway is evolutionarily conserved. In Hydra, HyGSK3 transcripts are strongly upregulated during gametogenesis. Treatment of female polyps with the GSK3 inhibitors lithium and alsterpaullone prevents the differentiation of nurse cells and subsequent oocyte formation. Our data indicate that GSK3 is required for the early induction of apoptosis in germline cells, which has been shown to be an initial step in Hydra gametogenesis. Our experiments show that main functions of GSK3 are evolutionarily conserved and unique to multicellular animals, a conclusion which is additionally supported by the presence of specific regulatory domains in the HyGSK3 protein.
Beschreibung:Gesehen am 10.05.2017
Beschreibung:Online Resource
ISSN:1095-564X
DOI:10.1016/j.ydbio.2004.10.007