Loss of the β-catenin homologue aardvark causes ectopic stalk formation in Dictyostelium

被引:28
作者
Coates, JC
Grimson, MJ
Williams, RSB
Bergman, W
Blanton, RL
Harwood, AJ
机构
[1] UCL, MRC, Mol Cell Biol Lab, London WC1E 6BT, England
[2] Texas Tech Univ, Dept Biol Sci, Lubbock, TX 79409 USA
基金
英国惠康基金; 英国医学研究理事会;
关键词
Dictyostelium; non-metazoan eukaryote; beta-catenin; aardvark; adherens junctions; stalk formation; cellulose stalk tube integrity; reporter gene expression;
D O I
10.1016/S0925-4773(02)00152-1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Aardvark (Aar) is a Dictyostelium P-catenin homologue with both cytoskeletal and signal transduction roles during development. Here, we show that loss of aar causes a novel phenotype where multiple stalks appear during late development. Ectopic stalks are preceded by misexpression of the stalk marker ST-lacZ in the surrounding tissue. This process does not involve the kinase GSK-3. Mixing experiments show that ectopic ST-lacZ expression and stalk formation are cell non-autonomous. The protein-cellulose matrix surrounding the stalk of aar mutant fruiting bodies is defective, and damage to the stalk of wild-type fruiting bodies leads to ectopic ST-lacZ expression. We postulate that poor synthesis of the stalk tube matrix allows diffusion of a stalk cell-inducing factor into the surrounding tissue. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:117 / 127
页数:11
相关论文
共 33 条
[31]   GROWTH OF MYXAMOEBAE OF CELLULAR SLIME MOULD DICTYOSTELIUM-DISCOIDEUM IN AXENIC CULTURE [J].
WATTS, DJ ;
ASHWORTH, JM .
BIOCHEMICAL JOURNAL, 1970, 119 (02) :171-&
[32]   ORIGINS OF THE PRESTALK-PRESPORE PATTERN IN DICTYOSTELIUM DEVELOPMENT [J].
WILLIAMS, JG ;
DUFFY, KT ;
LANE, DP ;
MCROBBIE, SJ ;
HARWOOD, AJ ;
TRAYNOR, D ;
KAY, RR ;
JERMYN, KA .
CELL, 1989, 59 (06) :1157-1163
[33]   Characterization of a Dictyostelium factor that acts synergistically with DIF to induce terminal stalk cell differentiation [J].
Yamada, Y ;
Okamoto, K ;
Williams, J .
DEVELOPMENTAL BIOLOGY, 1997, 184 (02) :296-302