Astral microtubule cross-linking safeguards uniform nuclear distribution in the Drosophila syncytium

J Cell Biol. 2022 Jan 3;221(1):e202007209. doi: 10.1083/jcb.202007209. Epub 2021 Nov 12.

Abstract

The early insect embryo develops as a multinucleated cell distributing the genome uniformly to the cell cortex. Mechanistic insight for nuclear positioning beyond cytoskeletal requirements is missing. Contemporary hypotheses propose actomyosin-driven cytoplasmic movement transporting nuclei or repulsion of neighbor nuclei driven by microtubule motors. Here, we show that microtubule cross-linking by Feo and Klp3A is essential for nuclear distribution and internuclear distance maintenance in Drosophila. Germline knockdown causes irregular, less-dense nuclear delivery to the cell cortex and smaller distribution in ex vivo embryo explants. A minimal internuclear distance is maintained in explants from control embryos but not from Feo-inhibited embryos, following micromanipulation-assisted repositioning. A dimerization-deficient Feo abolishes nuclear separation in embryo explants, while the full-length protein rescues the genetic knockdown. We conclude that Feo and Klp3A cross-linking of antiparallel microtubule overlap generates a length-regulated mechanical link between neighboring microtubule asters. Enabled by a novel experimental approach, our study illuminates an essential process of embryonic multicellularity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Nucleus / metabolism*
  • Cross-Linking Reagents / metabolism*
  • Drosophila Proteins / metabolism
  • Drosophila melanogaster / metabolism*
  • Embryo, Nonmammalian / metabolism
  • Giant Cells / metabolism*
  • Green Fluorescent Proteins / metabolism
  • Microtubules / metabolism*
  • RNA Interference
  • Time-Lapse Imaging

Substances

  • Cross-Linking Reagents
  • Drosophila Proteins
  • Green Fluorescent Proteins