GSK3 is a multifunctional regulator of Dictyostelium development

被引:33
作者
Schilde, C
Araki, T
Williams, H
Harwood, A
Williams, JG [1 ]
机构
[1] Univ Dundee, Wellcome Trust Bioctr, Sch Life Sci, Dundee DD1 5EH, Scotland
[2] UCL, MRC, Mol Cell Biol Lab, London WC1E 6BT, England
[3] UCL, Dept Biol, London WC1E 6BT, England
来源
DEVELOPMENT | 2004年 / 131卷 / 18期
关键词
GSK-3; Dictyostelium; cAMP; DIF; DIF-1; 2C gene;
D O I
10.1242/dev.01330
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 ecmB gene 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.
引用
收藏
页码:4555 / 4565
页数:11
相关论文
共 47 条
[1]   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 -: art. no. e107 [J].
Abe, T ;
Langenick, J ;
Williams, JG .
NUCLEIC ACIDS RESEARCH, 2003, 31 (18) :e107
[2]   PATTERNS OF CELL-MOVEMENT WITHIN THE DICTYOSTELIUM SLUG REVEALED BY CELL-TYPE-SPECIFIC, SURFACE LABELING OF LIVING CELLS [J].
ABE, T ;
EARLY, A ;
SIEGERT, F ;
WEIJER, C ;
WILLIAMS, J .
CELL, 1994, 77 (05) :687-699
[3]   A STAT-regulated, stress-induced signalling pathway in Dictyostelium [J].
Araki, T ;
Tsujioka, M ;
Abe, T ;
Fukuzawa, M ;
Meima, M ;
Schaap, P ;
Morio, T ;
Urushihara, H ;
Katoh, M ;
Maeda, M ;
Tanaka, Y ;
Takeuchi, I ;
Williams, JG .
JOURNAL OF CELL SCIENCE, 2003, 116 (14) :2907-2915
[4]   Developmentally and spatially regulated activation of a Dictyostelium STAT protein by a serpentine receptor [J].
Araki, T ;
Gamper, M ;
Early, A ;
Fukuzawa, M ;
Abe, T ;
Kawata, T ;
Kim, E ;
Firtel, RA ;
Williams, JG .
EMBO JOURNAL, 1998, 17 (14) :4018-4028
[5]  
BERKS M, 1990, DEVELOPMENT, V110, P977
[6]   TCF: Lady justice casting the final verdict on the outcome of Wnt signalling [J].
Brantjes, H ;
Barker, N ;
van Es, J ;
Clevers, H .
BIOLOGICAL CHEMISTRY, 2002, 383 (02) :255-261
[7]   Characterisation of a DNA sequence element that directs Dictyostelium stalk cell-specific gene expression [J].
Ceccarelli, A ;
Zhukovskaya, N ;
Kawata, T ;
Bozzaro, S ;
Williams, J .
DIFFERENTIATION, 2000, 66 (4-5) :189-196
[8]   Loss of the β-catenin homologue aardvark causes ectopic stalk formation in Dictyostelium [J].
Coates, JC ;
Grimson, MJ ;
Williams, RSB ;
Bergman, W ;
Blanton, RL ;
Harwood, AJ .
MECHANISMS OF DEVELOPMENT, 2002, 116 (1-2) :117-127
[9]   The renaissance of GSK3 [J].
Cohen, P ;
Frame, S .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2001, 2 (10) :769-776
[10]   DEVELOPMENTAL REGULATION OF CELL-TYPE-ENRICHED MESSENGER-RNAS IN DICTYOSTELIUM-DISCOIDEUM [J].
CORNEY, AJ ;
RICHARDS, AJ ;
PHILLPOTS, T ;
HAMES, BD .
MOLECULAR MICROBIOLOGY, 1990, 4 (04) :613-623