Role of BicDR in bristle shaft construction and support of BicD functions

Author:

Jejina Aleksandra12,Ayala Yeniffer3,Beuchle Dirk1,Höhener Thomas1,Dörig Ruth E.1,Vazquez-Pianzola Paula1,Hernández Greco3,Suter Beat1ORCID

Affiliation:

1. Institute of Cell Biology, University of Bern 1 , CH-3012 Bern , Switzerland

2. University of Bern 2 Graduate School for Cellular and Biomedical Sciences , , CH-3012 Bern , Switzerland

3. Unit of Biomedical Research on Cancer, Instituto Nacional de Cancerologıá (INCan) 3 Laboratory of Translation and Cancer , , 14080 Tlalpan, Mexico City , Mexico

Abstract

ABSTRACT Cell polarization requires asymmetric localization of numerous mRNAs, proteins and organelles. The movement of cargo towards the minus end of microtubules mostly depends on cytoplasmic dynein motors. In the dynein–dynactin–Bicaudal-D transport machinery, Bicaudal-D (BicD) links the cargo to the motor. Here, we focus on the role of Drosophila BicD-related (BicDR, CG32137) in the development of the long bristles. Together with BicD, it contributes to the organization and stability of the actin cytoskeleton in the not-yet-chitinized bristle shaft. BicD and BicDR also support the stable expression and distribution of Rab6 and Spn-F in the bristle shaft, including the distal tip localization of Spn-F, pointing to the role of microtubule-dependent vesicle trafficking for bristle construction. BicDR supports the function of BicD, and we discuss the hypothesis whereby BicDR might transport cargo more locally, with BicD transporting cargo over long distances, such as to the distal tip. We also identified embryonic proteins that interact with BicDR and appear to be BicDR cargo. For one of them, EF1γ (also known as eEF1γ), we show that the encoding gene EF1γ interacts with BicD and BicDR in the construction of the bristles.

Funder

Swiss National Science Foundation

University of Bern

Publisher

The Company of Biologists

Subject

Cell Biology

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