Experimental and Theoretical Evidence for Bidirectional Signaling via Core Planar Polarity Protein Complexes in Drosophila.
Biological Sciences
Developmental Biology
In Silico Biology
Journal
iScience
ISSN: 2589-0042
Titre abrégé: iScience
Pays: United States
ID NLM: 101724038
Informations de publication
Date de publication:
26 Jul 2019
26 Jul 2019
Historique:
received:
25
10
2018
revised:
21
03
2019
accepted:
12
06
2019
pubmed:
30
6
2019
medline:
30
6
2019
entrez:
30
6
2019
Statut:
ppublish
Résumé
In developing tissues, sheets of cells become planar polarized, enabling coordination of cell behaviors. It has been suggested that "signaling" of polarity information between cells may occur either bidirectionally or monodirectionally between the molecules Frizzled (Fz) and Van Gogh (Vang). Using computational modeling we find that both bidirectional and monodirectional signaling models reproduce known non-autonomous phenotypes derived from patches of mutant tissue of key molecules but predict different phenotypes from double mutant tissue, which have previously given conflicting experimental results. Furthermore, we re-examine experimental phenotypes in the Drosophila wing, concluding that signaling is most likely bidirectional. Our modeling suggests that bidirectional signaling can be mediated either indirectly via bidirectional feedbacks between asymmetric intercellular protein complexes or directly via different affinities for protein binding in intercellular complexes, suggesting future avenues for investigation. Our findings offer insight into mechanisms of juxtacrine cell signaling and how tissue-scale properties emerge from individual cell behaviors.
Identifiants
pubmed: 31254741
pii: S2589-0042(19)30204-4
doi: 10.1016/j.isci.2019.06.021
pmc: PMC6610702
pii:
doi:
Types de publication
Journal Article
Langues
eng
Pagination
49-66Subventions
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : NIH HHS
ID : P40 OD018537
Pays : United States
Informations de copyright
Copyright © 2019 The Author(s). Published by Elsevier Inc. All rights reserved.
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