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Prostaglandins temporally regulate cytoplasmic actin bundle formation during Drosophila oogenesis
Journal article   Open access   Peer reviewed

Prostaglandins temporally regulate cytoplasmic actin bundle formation during Drosophila oogenesis

Andrew J Spracklen, Daniel J Kelpsch, Xiang Chen, Cassandra N Spracklen and Tina L Tootle
Molecular biology of the cell, Vol.25(3), pp.397-411
02/01/2014
DOI: 10.1091/mbc.E13-07-0366
PMCID: PMC3907279
PMID: 24284900
url
https://doi.org/10.1091/mbc.E13-07-0366View
Published (Version of record) Open Access

Abstract

Tight regulation of actin remodeling is essential for development, and misregulation results in disease. Cytoskeletal dynamics are regulated by prostaglandins (PGs)—lipid signals. PGs temporally regulate actin remodeling during Drosophila oogenesis, at least in part, by modulating the activity of the actin elongation factor Enabled. Prostaglandins (PGs)—lipid signals produced downstream of cyclooxygenase (COX) enzymes—regulate actin dynamics in cell culture and platelets, but their roles during development are largely unknown. Here we define a new role for Pxt, the Drosophila COX-like enzyme, in regulating the actin cytoskeleton—temporal restriction of actin remodeling during oogenesis. PGs are required for actin filament bundle formation during stage 10B (S10B). In addition, loss of Pxt results in extensive early actin remodeling, including actin filaments and aggregates, within the posterior nurse cells of S9 follicles; wild-type follicles exhibit similar structures at a low frequency. Hu li tai shao (Hts-RC) and Villin (Quail), an actin bundler, localize to all early actin structures, whereas Enabled (Ena), an actin elongation factor, preferentially localizes to those in pxt mutants. Reduced Ena levels strongly suppress early actin remodeling in pxt mutants. Furthermore, loss of Pxt results in reduced Ena localization to the sites of bundle formation during S10B. Together these data lead to a model in which PGs temporally regulate actin remodeling during Drosophila oogenesis by controlling Ena localization/activity, such that in S9, PG signaling inhibits, whereas at S10B, it promotes Ena-dependent actin remodeling.

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