Assembly of endogenous oskar mRNA particles for motor-dependent transport in the Drosophila oocyte

Cell. 2009 Nov 25;139(5):983-98. doi: 10.1016/j.cell.2009.10.012.

Abstract

oskar mRNA localization at the oocyte posterior pole is essential for correct patterning of the Drosophila embryo. Here we show at the ultrastructural level that endogenous oskar ribonucleoprotein complexes (RNPs) assemble sequentially with initial recruitment of Hrp48 and the exon junction complex (EJC) to oskar transcripts in the nurse cell nuclei, and subsequent recruitment of Staufen and microtubule motors, following transport to the cytoplasm. oskar particles are non-membrane-bound structures that coalesce as they move from the oocyte anterior to the posterior pole. Our analysis uncovers a role for the EJC component Barentsz in recruiting Tropomyosin II (TmII) to oskar particles in the ooplasm and reveals that TmII is required for kinesin binding to the RNPs. Finally, we show that both kinesin and dynein associate with oskar particles and are the primary microtubule motors responsible for transport of the RNPs within the oocyte.

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Animals
  • Drosophila / metabolism*
  • Drosophila Proteins / metabolism*
  • Dyneins / metabolism
  • Heterogeneous-Nuclear Ribonucleoproteins / metabolism
  • Kinesins / metabolism
  • Microtubules / metabolism
  • Oocytes / metabolism*
  • RNA, Messenger / metabolism
  • RNA-Binding Proteins / metabolism
  • Ribonucleoproteins / metabolism*

Substances

  • Drosophila Proteins
  • Heterogeneous-Nuclear Ribonucleoproteins
  • Hrb27C protein, Drosophila
  • RNA, Messenger
  • RNA-Binding Proteins
  • Ribonucleoproteins
  • btz protein, Drosophila
  • osk protein, Drosophila
  • stau protein, Drosophila
  • Dyneins
  • Kinesins