Cargando…

Jak-Stat pathway induces Drosophila follicle elongation by a gradient of apical contractility

Tissue elongation and its control by spatiotemporal signals is a major developmental question. Currently, it is thought that Drosophila ovarian follicular epithelium elongation requires the planar polarization of the basal domain cytoskeleton and of the extra-cellular matrix, associated with a dynam...

Descripción completa

Detalles Bibliográficos
Autores principales: Alégot, Hervé, Pouchin, Pierre, Bardot, Olivier, Mirouse, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5805408/
https://www.ncbi.nlm.nih.gov/pubmed/29420170
http://dx.doi.org/10.7554/eLife.32943
_version_ 1783298968148508672
author Alégot, Hervé
Pouchin, Pierre
Bardot, Olivier
Mirouse, Vincent
author_facet Alégot, Hervé
Pouchin, Pierre
Bardot, Olivier
Mirouse, Vincent
author_sort Alégot, Hervé
collection PubMed
description Tissue elongation and its control by spatiotemporal signals is a major developmental question. Currently, it is thought that Drosophila ovarian follicular epithelium elongation requires the planar polarization of the basal domain cytoskeleton and of the extra-cellular matrix, associated with a dynamic process of rotation around the anteroposterior axis. Here we show, by careful kinetic analysis of fat2 mutants, that neither basal planar polarization nor rotation is required during a first phase of follicle elongation. Conversely, a JAK-STAT signaling gradient from each follicle pole orients early elongation. JAK-STAT controls apical pulsatile contractions, and Myosin II activity inhibition affects both pulses and early elongation. Early elongation is associated with apical constriction at the poles and with oriented cell rearrangements, but without any visible planar cell polarization of the apical domain. Thus, a morphogen gradient can trigger tissue elongation through a control of cell pulsing and without a planar cell polarity requirement.
format Online
Article
Text
id pubmed-5805408
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-58054082018-02-12 Jak-Stat pathway induces Drosophila follicle elongation by a gradient of apical contractility Alégot, Hervé Pouchin, Pierre Bardot, Olivier Mirouse, Vincent eLife Developmental Biology Tissue elongation and its control by spatiotemporal signals is a major developmental question. Currently, it is thought that Drosophila ovarian follicular epithelium elongation requires the planar polarization of the basal domain cytoskeleton and of the extra-cellular matrix, associated with a dynamic process of rotation around the anteroposterior axis. Here we show, by careful kinetic analysis of fat2 mutants, that neither basal planar polarization nor rotation is required during a first phase of follicle elongation. Conversely, a JAK-STAT signaling gradient from each follicle pole orients early elongation. JAK-STAT controls apical pulsatile contractions, and Myosin II activity inhibition affects both pulses and early elongation. Early elongation is associated with apical constriction at the poles and with oriented cell rearrangements, but without any visible planar cell polarization of the apical domain. Thus, a morphogen gradient can trigger tissue elongation through a control of cell pulsing and without a planar cell polarity requirement. eLife Sciences Publications, Ltd 2018-02-08 /pmc/articles/PMC5805408/ /pubmed/29420170 http://dx.doi.org/10.7554/eLife.32943 Text en © 2018, Alégot et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Alégot, Hervé
Pouchin, Pierre
Bardot, Olivier
Mirouse, Vincent
Jak-Stat pathway induces Drosophila follicle elongation by a gradient of apical contractility
title Jak-Stat pathway induces Drosophila follicle elongation by a gradient of apical contractility
title_full Jak-Stat pathway induces Drosophila follicle elongation by a gradient of apical contractility
title_fullStr Jak-Stat pathway induces Drosophila follicle elongation by a gradient of apical contractility
title_full_unstemmed Jak-Stat pathway induces Drosophila follicle elongation by a gradient of apical contractility
title_short Jak-Stat pathway induces Drosophila follicle elongation by a gradient of apical contractility
title_sort jak-stat pathway induces drosophila follicle elongation by a gradient of apical contractility
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5805408/
https://www.ncbi.nlm.nih.gov/pubmed/29420170
http://dx.doi.org/10.7554/eLife.32943
work_keys_str_mv AT alegotherve jakstatpathwayinducesdrosophilafollicleelongationbyagradientofapicalcontractility
AT pouchinpierre jakstatpathwayinducesdrosophilafollicleelongationbyagradientofapicalcontractility
AT bardotolivier jakstatpathwayinducesdrosophilafollicleelongationbyagradientofapicalcontractility
AT mirousevincent jakstatpathwayinducesdrosophilafollicleelongationbyagradientofapicalcontractility