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First published online 16 June 2009
doi: 10.1242/jcs.046482
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Research Article |
1 Program in Developmental Biology, Baylor College of Medicine, Houston, TX 77030, USA
2 Department of Biochemistry and Molecular Biology, University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA
3 Growth and Development, Biozentrum, University of Basel, CH-4056 Basel, Switzerland
4 Department of Systems Biology, University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA
5 Program in Genes and Development, University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA
* Author for correspondence (e-mail: ghalder{at}mdanderson.org)
Accepted 1 May 2009
The Hippo tumor-suppressor pathway controls tissue growth in Drosophila and mammals by regulating cell proliferation and apoptosis. The Hippo pathway includes the Fat cadherin, a transmembrane protein, which acts upstream of several other components that form a kinase cascade that culminates in the regulation of gene expression through the transcriptional coactivator Yorkie (Yki). Our previous work in Drosophila indicated that Merlin (Mer) and Expanded (Ex) are members of the Hippo pathway and act upstream of the Hippo kinase. In contrast to this model, it was suggested that Mer and Ex primarily regulate membrane dynamics and receptor trafficking, thereby affecting Hippo pathway activity only indirectly. Here, we examined the effects of Mer, Ex and the Hippo pathway on the size of the apical membrane and on apical-basal polarity complexes. We found that mer;ex double mutant imaginal disc cells have significantly increased levels of apical membrane determinants, such as Crb, aPKC and Patj. These phenotypes were shared with mutations in other Hippo pathway components and required Yki, indicating that Mer and Ex signal through the Hippo pathway. Interestingly, however, whereas Crb was required for the accumulation of other apical proteins and for the expansion of the apical domain observed in Hippo pathway mutants, its elimination did not significantly reverse the overgrowth phenotype of warts mutant cells. Therefore, Hippo signaling regulates cell polarity complexes in addition to and independently of its growth control function in imaginal disc cells.
Key words: Cell polarity, Drosophila, Growth control, Hippo
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