GSK3 is a multifunctional regulator of Dictyosteliumdevelopment
Author:
Schilde Christina1, Araki Tsuyoshi1, Williams Hazel2, Harwood Adrian2, Williams Jeffrey G.1
Affiliation:
1. School of Life Sciences, Wellcome Trust Biocentre, University of Dundee,Dundee DD1 5EH, UK 2. MRC Laboratory for Molecular Cell Biology and Department of Biology,University College, Gower Street, London WC1E 6BT, UK
Abstract
Glycogen synthase kinase 3 (GSK3) is a central regulator of metazoan development and the Dictyostelium GSK3 homologue, GskA, also controls cellular differentiation. The originally derived gskA-null mutant exhibits a severe pattern formation defect. It forms very large numbers of pre-basal disc cells at the expense of the prespore population. This defect arises early during multicellular development, making it impossible to examine later functions of GskA. We report the analysis of a gskA-null mutant, generated in a different parental strain, that proceeds through development to form mature fruiting bodies. In this strain, Ax2/gskA–,early development is accelerated and slug migration greatly curtailed. In a monolayer assay of stalk cell formation, the Ax2/gskA– strain is hypersensitive to the stalk cell-inducing action of DIF-1 but largely refractory to the repressive effect exerted by extracellular cAMP. During normal development, apically situated prestalk cells express the ecmBgene just as they commit themselves to stalk cell differentiation. In the Ax2/gskA– mutant, ecmB is expressed throughout the prestalk region of the slug, suggesting that GskA forms part of the repressive signalling pathway that prevents premature commitment to stalk cell differentiation. GskA may also play an inductive developmental role, because microarray analysis identifies a large gene family, the 2C family, that require gskA for optimal expression. These observations show that GskA functions throughout Dictyostelium development, to regulate several key aspects of cellular patterning.
Publisher
The Company of Biologists
Subject
Developmental Biology,Molecular Biology
Reference48 articles.
1. Abe, T., Early, A., Siegert, F., Weijer, C. and Williams, J.(1994). Patterns of cell movement within the Dictyostelium slug revealed by cell type-specific, surface labeling of living cells. Cell77,687-699. 2. Abe, T., Langenick, J. and Williams, J. G.(2003). Rapid generation of gene disruption constructs by in vitro transposition and identification of a Dictyostelium protein kinase that regulates its rate of growth and development. Nucleic Acids Res.31,e107. 3. Araki, T., Gamper, M., Early, A., Fukuzawa, M., Abe, T., Kawata,T., Kim, E., Firtel, R. A. and Williams, J. G. (1998). Developmentally and spatially regulated activation of a Dictyostelium STAT protein by a serpentine receptor. EMBO J.17,4018-4028. 4. Araki, T., Tsujioka, M., Abe, T., Fukuzawa, M., Meima, M.,Schaap, P., Morio, T., Urushihara, H., Katoh, M., Maeda, M. et al.(2003). A STAT-regulated, stress-induced signalling pathway in Dictyostelium. J. Cell Sci.116,2907-2915. 5. Berks, M. and Kay, R. R. (1990). Combinatorial control of cell differentiation by cAMP and DIF-1 during development of Dictyostelium discoideum. Development110,977-984.
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