Annexin B9 binds to βH-spectrin and is required for multivesicular body function in Drosophila

Monika Tjota, Seung Kyu Lee, Juan Wu, Janice A. Williams, Mansi R. Khanna, Graham H. Thomas

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)2914-2926
Number of pages13
JournalJournal of Cell Science
Volume124
Issue number17
DOIs
StatePublished - Sep 1 2011

All Science Journal Classification (ASJC) codes

  • Cell Biology

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