PUBLICATION

A role for Gle1, a regulator of DEAD-box RNA helicases, at centrosomes and basal bodies

Authors
Jao, L.E., Akef, A., Wente, S.R.
ID
ZDB-PUB-161231-4
Date
2017
Source
Molecular biology of the cell   28: 120-127 (Journal)
Registered Authors
Jao, Li-En, Wente, Susan R.
Keywords
none
MeSH Terms
  • Protein Binding
  • Nuclear Pore/metabolism
  • Basal Bodies/metabolism
  • RNA Transport
  • Centrosome/metabolism
  • RNA, Messenger/metabolism
  • Nuclear Pore Complex Proteins/metabolism
  • Zebrafish Proteins/metabolism*
  • Zebrafish Proteins/physiology*
  • DEAD-box RNA Helicases/metabolism
  • Antigens/metabolism
  • Adenosine Triphosphatases
  • Nucleocytoplasmic Transport Proteins/metabolism
  • RNA-Binding Proteins/metabolism*
  • RNA-Binding Proteins/physiology*
  • Active Transport, Cell Nucleus
PubMed
28035044 Full text @ Mol. Biol. Cell
Abstract
Control of organellar assembly and function is critical to eukaryotic homeostasis and survival. Gle1 is a highly conserved regulator of RNA-dependent DEAD-box ATPase proteins, with critical roles in both mRNA export and translation. In addition to its well-defined interaction with nuclear pore complexes, here we find that Gle1 is enriched at the centrosome and basal body. Gle1 assembles into the toroid-shaped pericentriolar material around the mother centriole. Reduced Gle1 levels are correlated with decreased pericentrin localization at the centrosome and microtubule organization defects. Of importance, these alterations in centrosome integrity do not result from loss of mRNA export. Examination of the Kupffer's vesicle in Gle1-depleted zebrafish revealed compromised ciliary beating and developmental defects. We propose that Gle1 assembly into the pericentriolar material positions the DEAD-box protein regulator to function in localized mRNA metabolism required for proper centrosome function.
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