An RNA-based feed-forward mechanism ensures motor switching in oskar mRNA transport

Author:

Gáspár Imre1ORCID,Phea Ly Jane1ORCID,McClintock Mark A.2ORCID,Heber Simone1ORCID,Bullock Simon L.2ORCID,Ephrussi Anne1ORCID

Affiliation:

1. Developmental Biology Unit, European Molecular Biology Laboratory 1 , Heidelberg, Germany

2. Division of Cell Biology, MRC Laboratory of Molecular Biology 2 , Cambridge, UK

Abstract

Regulated recruitment and activity of motor proteins is essential for intracellular transport of cargoes, including messenger ribonucleoprotein complexes (RNPs). Here, we show that orchestration of oskar RNP transport in the Drosophila germline relies on interplay between two double-stranded RNA-binding proteins, Staufen and the dynein adaptor Egalitarian (Egl). We find that Staufen antagonizes Egl-mediated transport of oskar mRNA by dynein both in vitro and in vivo. Following delivery of nurse cell-synthesized oskar mRNA into the oocyte by dynein, recruitment of Staufen to the RNPs results in dissociation of Egl and a switch to kinesin-1-mediated translocation of the mRNA to its final destination at the posterior pole of the oocyte. We additionally show that Egl associates with staufen (stau) mRNA in the nurse cells, mediating its enrichment and translation in the ooplasm. Our observations identify a novel feed-forward mechanism, whereby dynein-dependent accumulation of stau mRNA, and thus protein, in the oocyte enables motor switching on oskar RNPs by downregulating dynein activity.

Funder

Medical Research Council

Biotechnology and Biological Sciences Research Council

Deutsche Forschungsgemeinschaft

European Molecular Biology Laboratory

Publisher

Rockefeller University Press

Subject

Cell Biology

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