Notch-dependent epithelial fold determines boundary formation between developmental fields in the Drosophila antenna.

Compartment boundary formation plays an important role in development by separating adjacent developmental fields. Drosophila imaginal discs have proven valuable for studying the mechanisms of boundary formation. We studied the boundary separating the proximal A1 segment and the distal segments, def...

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Main Authors: Hui-Yu Ku, Y Henry Sun
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-07-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC5533456?pdf=render
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spelling doaj-78e94d09a08f4eda8e53faab6829379f2020-11-25T01:57:37ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042017-07-01137e100689810.1371/journal.pgen.1006898Notch-dependent epithelial fold determines boundary formation between developmental fields in the Drosophila antenna.Hui-Yu KuY Henry SunCompartment boundary formation plays an important role in development by separating adjacent developmental fields. Drosophila imaginal discs have proven valuable for studying the mechanisms of boundary formation. We studied the boundary separating the proximal A1 segment and the distal segments, defined respectively by Lim1 and Dll expression in the eye-antenna disc. Sharp segregation of the Lim1 and Dll expression domains precedes activation of Notch at the Dll/Lim1 interface. By repressing bantam miRNA and elevating the actin regulator Enable, Notch signaling then induces actomyosin-dependent apical constriction and epithelial fold. Disruption of Notch signaling or the actomyosin network reduces apical constriction and epithelial fold, so that Dll and Lim1 cells become intermingled. Our results demonstrate a new mechanism of boundary formation by actomyosin-dependent tissue folding, which provides a physical barrier to prevent mixing of cells from adjacent developmental fields.http://europepmc.org/articles/PMC5533456?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Hui-Yu Ku
Y Henry Sun
spellingShingle Hui-Yu Ku
Y Henry Sun
Notch-dependent epithelial fold determines boundary formation between developmental fields in the Drosophila antenna.
PLoS Genetics
author_facet Hui-Yu Ku
Y Henry Sun
author_sort Hui-Yu Ku
title Notch-dependent epithelial fold determines boundary formation between developmental fields in the Drosophila antenna.
title_short Notch-dependent epithelial fold determines boundary formation between developmental fields in the Drosophila antenna.
title_full Notch-dependent epithelial fold determines boundary formation between developmental fields in the Drosophila antenna.
title_fullStr Notch-dependent epithelial fold determines boundary formation between developmental fields in the Drosophila antenna.
title_full_unstemmed Notch-dependent epithelial fold determines boundary formation between developmental fields in the Drosophila antenna.
title_sort notch-dependent epithelial fold determines boundary formation between developmental fields in the drosophila antenna.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2017-07-01
description Compartment boundary formation plays an important role in development by separating adjacent developmental fields. Drosophila imaginal discs have proven valuable for studying the mechanisms of boundary formation. We studied the boundary separating the proximal A1 segment and the distal segments, defined respectively by Lim1 and Dll expression in the eye-antenna disc. Sharp segregation of the Lim1 and Dll expression domains precedes activation of Notch at the Dll/Lim1 interface. By repressing bantam miRNA and elevating the actin regulator Enable, Notch signaling then induces actomyosin-dependent apical constriction and epithelial fold. Disruption of Notch signaling or the actomyosin network reduces apical constriction and epithelial fold, so that Dll and Lim1 cells become intermingled. Our results demonstrate a new mechanism of boundary formation by actomyosin-dependent tissue folding, which provides a physical barrier to prevent mixing of cells from adjacent developmental fields.
url http://europepmc.org/articles/PMC5533456?pdf=render
work_keys_str_mv AT huiyuku notchdependentepithelialfolddeterminesboundaryformationbetweendevelopmentalfieldsinthedrosophilaantenna
AT yhenrysun notchdependentepithelialfolddeterminesboundaryformationbetweendevelopmentalfieldsinthedrosophilaantenna
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