Cortical microtubule nucleation can organise the cytoskeleton of Drosophila oocytes to define the anteroposterior axis

Many cells contain non-centrosomal arrays of microtubules (MTs), but the assembly, organisation and function of these arrays are poorly understood. We present the first theoretical model for the non-centrosomal MT cytoskeleton in Drosophila oocytes, in which bicoid and oskar mRNAs become localised t...

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Bibliographic Details
Main Authors: Khuc Trong, Philipp (Author), Dunkel, Joern (Contributor), Doerflinger, Helene (Author), St. Johnston, Daniel (Author), Goldstein, Raymond E. (Author)
Other Authors: Massachusetts Institute of Technology. Department of Mathematics (Contributor)
Format: Article
Language:English
Published: eLife Sciences Publications, Ltd., 2015-11-02T20:03:05Z.
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Online Access:Get fulltext
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100 1 0 |a Khuc Trong, Philipp  |e author 
100 1 0 |a Massachusetts Institute of Technology. Department of Mathematics  |e contributor 
100 1 0 |a Dunkel, Joern  |e contributor 
700 1 0 |a Dunkel, Joern  |e author 
700 1 0 |a Doerflinger, Helene  |e author 
700 1 0 |a St. Johnston, Daniel  |e author 
700 1 0 |a Goldstein, Raymond E.  |e author 
245 0 0 |a Cortical microtubule nucleation can organise the cytoskeleton of Drosophila oocytes to define the anteroposterior axis 
260 |b eLife Sciences Publications, Ltd.,   |c 2015-11-02T20:03:05Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/99665 
520 |a Many cells contain non-centrosomal arrays of microtubules (MTs), but the assembly, organisation and function of these arrays are poorly understood. We present the first theoretical model for the non-centrosomal MT cytoskeleton in Drosophila oocytes, in which bicoid and oskar mRNAs become localised to establish the anterior-posterior body axis. Constrained by experimental measurements, the model shows that a simple gradient of cortical MT nucleation is sufficient to reproduce the observed MT distribution, cytoplasmic flow patterns and localisation of oskar and naive bicoid mRNAs. Our simulations exclude a major role for cytoplasmic flows in localisation and reveal an organisation of the MT cytoskeleton that is more ordered than previously thought. Furthermore, modulating cortical MT nucleation induces a bifurcation in cytoskeletal organisation that accounts for the phenotypes of polarity mutants. Thus, our three-dimensional model explains many features of the MT network and highlights the importance of differential cortical MT nucleation for axis formation. 
520 |a Solomon Buchsbaum AT&T Research Fund 
546 |a en_US 
655 7 |a Article 
773 |t eLife