Two types of asymmetric divisions in the Drosophila sensory organ precursor cell lineage

Author:  ["Fabrice Roegiers","Susan Younger-Shepherd","Lily Yeh Jan","Yuh Nung Jan"]

Publication:  Nature Cell Biology

CITE.CC academic search helps you expand the influence of your papers.

Tags:  general   CellBiology   CancerResearch   DevelopmentalBiology   StemCells   Biological

Abstract

Asymmetric partitioning of cell-fate determinants during development requires coordinating the positioning of these determinants with orientation of the mitotic spindle. In the Drosophila peripheral nervous system, sensory organ progenitor cells (SOPs) undergo several rounds of division to produce five cells that give rise to a complete sensory organ. Here we have observed the asymmetric divisions that give rise to these cells in the developing pupae using green fluorescent protein fusion proteins. We find that spindle orientation and determinant localization are tightly coordinated at each division. Furthermore, we find that two types of asymmetric divisions exist within the sensory organ precursor cell lineage: the anterior–posterior pI cell-type division, where the spindle remains symmetric throughout mitosis, and the strikingly neuroblast-like apical–basal division of the pIIb cell, where the spindle exhibits a strong asymmetry at anaphase. In both these divisions, the spindle reorientates to position itself perpendicular to the region of the cortex containing the determinant. On the basis of these observations, we propose that two distinct mechanisms for controlling asymmetric cell divisions occur within the same lineage in the developing peripheral nervous system in Drosophila.

Cite this article

Roegiers, F., Younger-Shepherd, S., Jan, L. et al. Two types of asymmetric divisions in the Drosophila sensory organ precursor cell lineage. Nat Cell Biol 3, 58–67 (2001). https://doi.org/10.1038/35050568

View full text

>> Full Text:   Two types of asymmetric divisions in the Drosophila sensory organ precursor cell lineage

Frizzled regulates localization of cell-fate determinants and mitotic spindle rotation during asymme

Hrd1p/Der3p is a membrane-anchored ubiquitin ligase required for ER-associated degradation