Affiliations 

  • 1 Laboratory for Neurodiversity, RIKEN Center for Brain Science, Wako-shi, Saitama 351-0198, Japan
  • 2 Laboratory for Neurodiversity, RIKEN Center for Brain Science, Wako-shi, Saitama 351-0198, Japan; School of Health Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan 16150, Malaysia
  • 3 Department of Computer Science, Brandeis University, Boston, MA 02453, USA
  • 4 Laboratory for Neurodiversity, RIKEN Center for Brain Science, Wako-shi, Saitama 351-0198, Japan. Electronic address: adrian.moore@riken.jp
Neuron, 2020 05 06;106(3):452-467.e8.
PMID: 32155441 DOI: 10.1016/j.neuron.2020.02.002

Abstract

Dendrite arbor pattern determines the functional characteristics of a neuron. It is founded on primary branch structure, defined through cell intrinsic and transcription-factor-encoded mechanisms. Developing arbors have extensive acentrosomal microtubule dynamics, and here, we report an unexpected role for the atypical actin motor Myo6 in creating primary branch structure by specifying the position, polarity, and targeting of these events. We carried out in vivo time-lapse imaging of Drosophila adult sensory neuron differentiation, integrating machine-learning-based quantification of arbor patterning with molecular-level tracking of cytoskeletal remodeling. This revealed that Myo6 and the transcription factor Knot regulate transient surges of microtubule polymerization at dendrite tips; they drive retrograde extension of an actin filament array that specifies anterograde microtubule polymerization and guides these microtubules to subdivide the tip into multiple branches. Primary branches delineate functional compartments; this tunable branching mechanism is key to define and diversify dendrite arbor compartmentalization.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.