The hippo pathway promotes Notch signaling in regulation of cell differentiation, proliferation, and oocyte polarity.

Specification of the anterior-posterior axis in Drosophila oocytes requires proper communication between the germ-line cells and the somatically derived follicular epithelial cells. Multiple signaling pathways, including Notch, contribute to oocyte polarity formation by controlling the temporal and...

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Main Authors: Jianzhong Yu, John Poulton, Yi-Chun Huang, Wu-Min Deng
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-03-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2258146?pdf=render
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spelling doaj-08d2c8510cee4f43b8daf7041f6de6cf2020-11-24T21:34:05ZengPublic Library of Science (PLoS)PLoS ONE1932-62032008-03-0133e176110.1371/journal.pone.0001761The hippo pathway promotes Notch signaling in regulation of cell differentiation, proliferation, and oocyte polarity.Jianzhong YuJohn PoultonYi-Chun HuangWu-Min DengSpecification of the anterior-posterior axis in Drosophila oocytes requires proper communication between the germ-line cells and the somatically derived follicular epithelial cells. Multiple signaling pathways, including Notch, contribute to oocyte polarity formation by controlling the temporal and spatial pattern of follicle cell differentiation and proliferation. Here we show that the newly identified Hippo tumor-suppressor pathway plays a crucial role in the posterior follicle cells in the regulation of oocyte polarity. Disruption of the Hippo pathway, including major components Hippo, Salvador, and Warts, results in aberrant follicle-cell differentiation and proliferation and dramatic disruption of the oocyte anterior-posterior axis. These phenotypes are related to defective Notch signaling in follicle cells, because misexpression of a constitutively active form of Notch alleviates the oocyte polarity defects. We also find that follicle cells defective in Hippo signaling accumulate the Notch receptor and display defects in endocytosis markers. Our findings suggest that the interaction between Hippo and classic developmental pathways such as Notch is critical to spatial and temporal regulation of differentiation and proliferation and is essential for development of the body axes in Drosophila.http://europepmc.org/articles/PMC2258146?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jianzhong Yu
John Poulton
Yi-Chun Huang
Wu-Min Deng
spellingShingle Jianzhong Yu
John Poulton
Yi-Chun Huang
Wu-Min Deng
The hippo pathway promotes Notch signaling in regulation of cell differentiation, proliferation, and oocyte polarity.
PLoS ONE
author_facet Jianzhong Yu
John Poulton
Yi-Chun Huang
Wu-Min Deng
author_sort Jianzhong Yu
title The hippo pathway promotes Notch signaling in regulation of cell differentiation, proliferation, and oocyte polarity.
title_short The hippo pathway promotes Notch signaling in regulation of cell differentiation, proliferation, and oocyte polarity.
title_full The hippo pathway promotes Notch signaling in regulation of cell differentiation, proliferation, and oocyte polarity.
title_fullStr The hippo pathway promotes Notch signaling in regulation of cell differentiation, proliferation, and oocyte polarity.
title_full_unstemmed The hippo pathway promotes Notch signaling in regulation of cell differentiation, proliferation, and oocyte polarity.
title_sort hippo pathway promotes notch signaling in regulation of cell differentiation, proliferation, and oocyte polarity.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2008-03-01
description Specification of the anterior-posterior axis in Drosophila oocytes requires proper communication between the germ-line cells and the somatically derived follicular epithelial cells. Multiple signaling pathways, including Notch, contribute to oocyte polarity formation by controlling the temporal and spatial pattern of follicle cell differentiation and proliferation. Here we show that the newly identified Hippo tumor-suppressor pathway plays a crucial role in the posterior follicle cells in the regulation of oocyte polarity. Disruption of the Hippo pathway, including major components Hippo, Salvador, and Warts, results in aberrant follicle-cell differentiation and proliferation and dramatic disruption of the oocyte anterior-posterior axis. These phenotypes are related to defective Notch signaling in follicle cells, because misexpression of a constitutively active form of Notch alleviates the oocyte polarity defects. We also find that follicle cells defective in Hippo signaling accumulate the Notch receptor and display defects in endocytosis markers. Our findings suggest that the interaction between Hippo and classic developmental pathways such as Notch is critical to spatial and temporal regulation of differentiation and proliferation and is essential for development of the body axes in Drosophila.
url http://europepmc.org/articles/PMC2258146?pdf=render
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