TY - JOUR
T1 - Early endosome motility spatially organizes polysome distribution
AU - Higuchi, Yujiro
AU - Ashwin, Peter
AU - Roger, Yvonne
AU - Steinberg, Gero
PY - 2014/2/3
Y1 - 2014/2/3
N2 - Early endosomes (EEs) mediate protein sorting, and their cytoskeleton-dependent motility supports longdistance signaling in neurons. Here, we report an unexpected role of EE motility in distributing the translation machinery in a fungal model system. We visualize ribosomal subunit proteins and show that the large subunits diffused slowly throughout the cytoplasm (Dc,60S = 0.311 μm2/s), whereas entire polysomes underwent long-range motility along microtubules. This movement was mediated by "hitchhiking" on kinesin-3 and dyneindriven EEs, where the polysomes appeared to translate EE-associated mRNA into proteins. Modeling indicates that this motor-driven transport is required for even cellular distribution of newly formed ribosomes. Indeed, impaired EE motility in motor mutants, or their inability to bind EEs in mutants lacking the RNA-binding protein Rrm4, reduced ribosome transport and induced ribosome aggregation near the nucleus. As a consequence, cell growth was severely restricted. Collectively, our results indicate that polysomes associate with moving EEs and that "off- and reloading" distributes the protein translation machinery.
AB - Early endosomes (EEs) mediate protein sorting, and their cytoskeleton-dependent motility supports longdistance signaling in neurons. Here, we report an unexpected role of EE motility in distributing the translation machinery in a fungal model system. We visualize ribosomal subunit proteins and show that the large subunits diffused slowly throughout the cytoplasm (Dc,60S = 0.311 μm2/s), whereas entire polysomes underwent long-range motility along microtubules. This movement was mediated by "hitchhiking" on kinesin-3 and dyneindriven EEs, where the polysomes appeared to translate EE-associated mRNA into proteins. Modeling indicates that this motor-driven transport is required for even cellular distribution of newly formed ribosomes. Indeed, impaired EE motility in motor mutants, or their inability to bind EEs in mutants lacking the RNA-binding protein Rrm4, reduced ribosome transport and induced ribosome aggregation near the nucleus. As a consequence, cell growth was severely restricted. Collectively, our results indicate that polysomes associate with moving EEs and that "off- and reloading" distributes the protein translation machinery.
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U2 - 10.1083/jcb.201307164
DO - 10.1083/jcb.201307164
M3 - Article
C2 - 24493587
AN - SCOPUS:84893460580
SN - 0021-9525
VL - 204
SP - 343
EP - 357
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 3
ER -