Two populations of cytoplasmic dynein contribute to spindle positioning in C. elegans embryos

J Cell Biol. 2017 Sep 4;216(9):2777-2793. doi: 10.1083/jcb.201607038. Epub 2017 Jul 24.

Abstract

The position of the mitotic spindle is tightly controlled in animal cells as it determines the plane and orientation of cell division. Contacts between cytoplasmic dynein and astral microtubules (MTs) at the cell cortex generate pulling forces that position the spindle. An evolutionarily conserved Gα-GPR-1/2Pins/LGN-LIN-5Mud/NuMA cortical complex interacts with dynein and is required for pulling force generation, but the dynamics of this process remain unclear. In this study, by fluorescently labeling endogenous proteins in Caenorhabditis elegans embryos, we show that dynein exists in two distinct cortical populations. One population directly depends on LIN-5, whereas the other is concentrated at MT plus ends and depends on end-binding (EB) proteins. Knockout mutants lacking all EBs are viable and fertile and display normal pulling forces and spindle positioning. However, EB protein-dependent dynein plus end tracking was found to contribute to force generation in embryos with a partially perturbed dynein function, indicating the existence of two mechanisms that together create a highly robust force-generating system.

Publication types

  • Video-Audio Media
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Caenorhabditis elegans / embryology
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / metabolism*
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism*
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism
  • Cytoplasm / metabolism*
  • Cytoplasmic Dyneins / genetics
  • Cytoplasmic Dyneins / metabolism*
  • Genotype
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Microscopy, Fluorescence
  • Microscopy, Video
  • Microtubules / genetics
  • Microtubules / metabolism
  • Mutation
  • Phenotype
  • Recombinant Fusion Proteins / metabolism
  • Red Fluorescent Protein
  • Signal Transduction
  • Spindle Apparatus / genetics
  • Spindle Apparatus / metabolism*
  • Time Factors

Substances

  • Caenorhabditis elegans Proteins
  • Cell Cycle Proteins
  • Luminescent Proteins
  • Recombinant Fusion Proteins
  • enhanced green fluorescent protein
  • lin-5 protein, C elegans
  • Green Fluorescent Proteins
  • Cytoplasmic Dyneins
  • DHC-1 protein, C elegans