Affiliation:
1. Departments of Biology and of Biochemistry and Molecluar Biology, 208 Mueller Laboratory, The Pennsylvania State University, University Park, PA 16802, USA
Abstract
The role of the cytoskeleton in protein trafficking is still being defined. Here, we describe a relationship between the small Ca2+-dependent membrane-binding protein Annexin B9 (AnxB9), apical βHeavy-spectrin (βH) and the multivesicular body (MVB) in Drosophila. AnxB9 binds to a subset of βH spliceoforms, and loss of AnxB9 results in an increase in basolateral βH and its appearance on cytoplasmic vesicles that overlap with the MVB markers Hrs, Vps16 and EPS15. Similar colocalizations are seen when βH-positive endosomes are generated either by upregulation of βH in pak mutants or through the expression of the dominant-negative version of βH. In common with other mutations disrupting the MVB, we also show that there is an accumulation of ubiquitylated proteins and elevated EGFR signaling in the absence of AnxB9 or βH. Loss of AnxB9 or βH function also causes the redistribution of the DE-Cadherin (encoded by shotgun) to endosomal vesicles, suggesting a rationale for the previously documented destabilization of the zonula adherens in karst (which encodes βH) mutants. Reduction of AnxB9 results in degradation of the apical–lateral boundary and the appearance of the basolateral proteins Coracle and Dlg on internal vesicles adjacent to βH. These results indicate that AnxB9 and βH are intimately involved in endosomal trafficking to the MVB and play a role in maintaining high-fidelity segregation of the apical and lateral domains.
Publisher
The Company of Biologists
Cited by
22 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献