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Asymmetric localization of DLC1 defines avian trunk neural crest polarity for directional delamination and migration.


ABSTRACT: Following epithelial-mesenchymal transition, acquisition of avian trunk neural crest cell (NCC) polarity is prerequisite for directional delamination and migration, which in turn is essential for peripheral nervous system development. However, how this cell polarization is established and regulated remains unknown. Here we demonstrate that, using the RHOA biosensor in vivo and in vitro, the initiation of NCC polarization is accompanied by highly activated RHOA in the cytoplasm at the cell rear and its fluctuating activity at the front edge. This differential RHOA activity determines polarized NC morphology and motility, and is regulated by the asymmetrically localized RhoGAP Deleted in liver cancer (DLC1) in the cytoplasm at the cell front. Importantly, the association of DLC1 with NEDD9 is crucial for its asymmetric localization and differential RHOA activity. Moreover, NC specifiers, SOX9 and SOX10, regulate NEDD9 and DLC1 expression, respectively. These results present a SOX9/SOX10-NEDD9/DLC1-RHOA regulatory axis to govern NCC migratory polarization.

SUBMITTER: Liu JA 

PROVIDER: S-EPMC5662599 | biostudies-literature | 2017 Oct

REPOSITORIES: biostudies-literature

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Asymmetric localization of DLC1 defines avian trunk neural crest polarity for directional delamination and migration.

Liu Jessica Aijia JA   Rao Yanxia Y   Cheung May Pui Lai MPL   Hui Man-Ning MN   Wu Ming-Hoi MH   Chan Lo-Kong LK   Ng Irene Oi-Lin IO   Niu Ben B   Cheah Kathryn S E KSE   Sharma Rakesh R   Hodgson Louis L   Cheung Martin M  

Nature communications 20171030 1


Following epithelial-mesenchymal transition, acquisition of avian trunk neural crest cell (NCC) polarity is prerequisite for directional delamination and migration, which in turn is essential for peripheral nervous system development. However, how this cell polarization is established and regulated remains unknown. Here we demonstrate that, using the RHOA biosensor in vivo and in vitro, the initiation of NCC polarization is accompanied by highly activated RHOA in the cytoplasm at the cell rear a  ...[more]

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