Cargando…

The Exocyst Component Sec3 Controls Egg Chamber Development Through Notch During Drosophila Oogenesis

The exocyst complex plays multiple roles via tethering secretory or recycling vesicles to the plasma membrane. Previous studies have demonstrated that the exocyst contains eight components, which possibly have some redundant but distinct functions. It is therefore interesting to investigate the biol...

Descripción completa

Detalles Bibliográficos
Autores principales: Wan, Ping, Zheng, Sumei, Chen, Lai, Wang, Dou, Liao, Ting, Yan, Xueming, Wang, Xiaoji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450198/
https://www.ncbi.nlm.nih.gov/pubmed/30984026
http://dx.doi.org/10.3389/fphys.2019.00345
_version_ 1783408993198145536
author Wan, Ping
Zheng, Sumei
Chen, Lai
Wang, Dou
Liao, Ting
Yan, Xueming
Wang, Xiaoji
author_facet Wan, Ping
Zheng, Sumei
Chen, Lai
Wang, Dou
Liao, Ting
Yan, Xueming
Wang, Xiaoji
author_sort Wan, Ping
collection PubMed
description The exocyst complex plays multiple roles via tethering secretory or recycling vesicles to the plasma membrane. Previous studies have demonstrated that the exocyst contains eight components, which possibly have some redundant but distinct functions. It is therefore interesting to investigate the biological function of each component. Here, we found that Sec3, one component of exocyst complex, is involved in Drosophila egg chamber development. Loss of sec3 results in egg chamber fusion through the abolishment of cell differentiation. In addition, loss of sec3 increases cell numbers but decreases cell size. These defects phenocopy Notch pathway inactivation. In line with this, loss of sec3 indeed leads to Notch protein accumulation, suggesting that the loss of Sec3 inhibits the delivery of Notch onto the plasma membrane and accumulates inactive Notch in the cytoplasm. Loss of sec3 also leads to the ectopic expression of two Notch pathway target genes, Cut and FasciclinIII, which should normally be downregulated by Notch. Altogether, our study revealed that Sec3 governs egg chamber development through the regulation of Notch, and provides fresh insights into the regulation of oogenesis.
format Online
Article
Text
id pubmed-6450198
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-64501982019-04-12 The Exocyst Component Sec3 Controls Egg Chamber Development Through Notch During Drosophila Oogenesis Wan, Ping Zheng, Sumei Chen, Lai Wang, Dou Liao, Ting Yan, Xueming Wang, Xiaoji Front Physiol Physiology The exocyst complex plays multiple roles via tethering secretory or recycling vesicles to the plasma membrane. Previous studies have demonstrated that the exocyst contains eight components, which possibly have some redundant but distinct functions. It is therefore interesting to investigate the biological function of each component. Here, we found that Sec3, one component of exocyst complex, is involved in Drosophila egg chamber development. Loss of sec3 results in egg chamber fusion through the abolishment of cell differentiation. In addition, loss of sec3 increases cell numbers but decreases cell size. These defects phenocopy Notch pathway inactivation. In line with this, loss of sec3 indeed leads to Notch protein accumulation, suggesting that the loss of Sec3 inhibits the delivery of Notch onto the plasma membrane and accumulates inactive Notch in the cytoplasm. Loss of sec3 also leads to the ectopic expression of two Notch pathway target genes, Cut and FasciclinIII, which should normally be downregulated by Notch. Altogether, our study revealed that Sec3 governs egg chamber development through the regulation of Notch, and provides fresh insights into the regulation of oogenesis. Frontiers Media S.A. 2019-03-29 /pmc/articles/PMC6450198/ /pubmed/30984026 http://dx.doi.org/10.3389/fphys.2019.00345 Text en Copyright © 2019 Wan, Zheng, Chen, Wang, Liao, Yan and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Wan, Ping
Zheng, Sumei
Chen, Lai
Wang, Dou
Liao, Ting
Yan, Xueming
Wang, Xiaoji
The Exocyst Component Sec3 Controls Egg Chamber Development Through Notch During Drosophila Oogenesis
title The Exocyst Component Sec3 Controls Egg Chamber Development Through Notch During Drosophila Oogenesis
title_full The Exocyst Component Sec3 Controls Egg Chamber Development Through Notch During Drosophila Oogenesis
title_fullStr The Exocyst Component Sec3 Controls Egg Chamber Development Through Notch During Drosophila Oogenesis
title_full_unstemmed The Exocyst Component Sec3 Controls Egg Chamber Development Through Notch During Drosophila Oogenesis
title_short The Exocyst Component Sec3 Controls Egg Chamber Development Through Notch During Drosophila Oogenesis
title_sort exocyst component sec3 controls egg chamber development through notch during drosophila oogenesis
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450198/
https://www.ncbi.nlm.nih.gov/pubmed/30984026
http://dx.doi.org/10.3389/fphys.2019.00345
work_keys_str_mv AT wanping theexocystcomponentsec3controlseggchamberdevelopmentthroughnotchduringdrosophilaoogenesis
AT zhengsumei theexocystcomponentsec3controlseggchamberdevelopmentthroughnotchduringdrosophilaoogenesis
AT chenlai theexocystcomponentsec3controlseggchamberdevelopmentthroughnotchduringdrosophilaoogenesis
AT wangdou theexocystcomponentsec3controlseggchamberdevelopmentthroughnotchduringdrosophilaoogenesis
AT liaoting theexocystcomponentsec3controlseggchamberdevelopmentthroughnotchduringdrosophilaoogenesis
AT yanxueming theexocystcomponentsec3controlseggchamberdevelopmentthroughnotchduringdrosophilaoogenesis
AT wangxiaoji theexocystcomponentsec3controlseggchamberdevelopmentthroughnotchduringdrosophilaoogenesis
AT wanping exocystcomponentsec3controlseggchamberdevelopmentthroughnotchduringdrosophilaoogenesis
AT zhengsumei exocystcomponentsec3controlseggchamberdevelopmentthroughnotchduringdrosophilaoogenesis
AT chenlai exocystcomponentsec3controlseggchamberdevelopmentthroughnotchduringdrosophilaoogenesis
AT wangdou exocystcomponentsec3controlseggchamberdevelopmentthroughnotchduringdrosophilaoogenesis
AT liaoting exocystcomponentsec3controlseggchamberdevelopmentthroughnotchduringdrosophilaoogenesis
AT yanxueming exocystcomponentsec3controlseggchamberdevelopmentthroughnotchduringdrosophilaoogenesis
AT wangxiaoji exocystcomponentsec3controlseggchamberdevelopmentthroughnotchduringdrosophilaoogenesis