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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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 |
_version_ |
1724973750523265024 |