Akt regulates centrosome migration and spindle orientation in the early Drosophila melanogaster embryo

Author:

Buttrick Graham J.1,Beaumont Luke M.A.23,Leitch Jessica3,Yau Christopher3,Hughes Julian R.1,Wakefield James G.13

Affiliation:

1. Department of Zoology, University of Oxford, Oxford OX1 3PS, England, UK

2. Department of Engineering, University of Oxford, Oxford OX1 3PJ, England, UK

3. Life Sciences Interface Doctoral Training Centre, University of Oxford, Oxford OX1 3QD, England, UK

Abstract

Correct positioning and morphology of the mitotic spindle is achieved through regulating the interaction between microtubules (MTs) and cortical actin. Here we find that, in the Drosophila melanogaster early embryo, reduced levels of the protein kinase Akt result in incomplete centrosome migration around cortical nuclei, bent mitotic spindles, and loss of nuclei into the interior of the embryo. We show that Akt is enriched at the embryonic cortex and is required for phosphorylation of the glycogen synthase kinase-3β homologue Zeste-white 3 kinase (Zw3) and for the cortical localizations of the adenomatosis polyposis coli (APC)–related protein APC2/E-APC and the MT + Tip protein EB1. We also show that reduced levels of Akt result in mislocalization of APC2 in postcellularized embryonic mitoses and misorientation of epithelial mitotic spindles. Together, our results suggest that Akt regulates a complex containing Zw3, Armadillo, APC2, and EB1 and that this complex has a role in stabilizing MT–cortex interactions, facilitating both centrosome separation and mitotic spindle orientation.

Publisher

Rockefeller University Press

Subject

Cell Biology

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