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Published online
doi:10.1083/jcb.200812146
The Journal of Cell Biology, Vol. 185, No. 5, 787-796
The Rockefeller University Press, 0021-9525 $30.00
© McGill et al.
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Independent cadherin–catenin and Bazooka clusters interact to assemble adherens junctions



Melanie A. McGill, R.F. Andrew McKinley, and Tony J.C. Harris

Department of Cell and Systems Biology, University of Toronto, Toronto, Ontario M5S 3G5, Canada

Correspondence to Tony J.C. Harris: tony.harris{at}utoronto.ca

Proper epithelial structure requires adherens junction (AJ) assembly. In the early Drosophila embryo, AJ assembly depends on Bazooka (Baz; PAR-3), but it is unclear how Baz affects AJ assembly and what precursors are involved. To understand this process at the molecular level, we counted the number of core AJ proteins and Baz proteins at an average spot AJ (SAJ) and determined their dynamics with fluorescence recovery after photobleaching experiments. These data reveal that SAJs are subdivided into Baz clusters and cadherin–catenin clusters with independent protein numbers and dynamics. This independence suggests that precursory cadherin–catenin clusters might form before SAJ assembly. We identify cadherin–catenin clusters forming between apical microvilli. Further analyses show that they form independently of Baz and that Baz functions in repositioning them to apicolateral sites for full SAJ assembly. Our data implicate cell protrusions in initial cadherin–catenin clustering in the Drosophila melanogaster embryo. Then, independent Baz clusters appear to engage the cadherin–catenin clusters to assemble SAJs.


M.A. McGill and R.F.A. McKinley contributed equally to this paper.

Abbreviations used in this paper: AJ, adherens junction; Arm, Armadillo; Baz, Bazooka; BJ, basal junction; DE-cad, Drosophila E-cadherin; IM, intervening membrane; MT, microtubule; RFI, relative fluorescent intensity; SAJ, spot AJ; WT, wild type.

© 2009 McGill et al.
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