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A protocadherin-cadherin-FLRT3 complex controls cell adhesion and morphogenesis

Authors
 Xuejun Chen  ;  Eunjin Koh  ;  Michael Yoder  ;  Barry M. Gumbiner 
Citation
 PLOS ONE, Vol.4(12) : e8411, 2009 
Journal Title
 PLOS ONE 
Issue Date
2009
MeSH
Animals ; CHO Cells ; Cadherins/metabolism* ; Cell Adhesion ; Cricetinae ; Cricetulus ; Embryo, Nonmammalian/cytology* ; Embryo, Nonmammalian/metabolism ; Flow Cytometry ; Gene Knockdown Techniques ; Humans ; Immunoprecipitation ; Membrane Proteins/antagonists & inhibitors ; Membrane Proteins/metabolism* ; Morphogenesis* ; Protein Binding ; Protein Transport ; Xenopus Proteins/antagonists & inhibitors ; Xenopus Proteins/metabolism* ; Xenopus laevis/embryology* ; Xenopus laevis/metabolism ; rho GTP-Binding Proteins/metabolism
Abstract
BACKGROUND: Paraxial protocadherin (PAPC) and fibronectin leucine-rich domain transmembrane protein-3 (FLRT3) are induced by TGFbeta signaling in Xenopus embryos and both regulate morphogenesis by inhibiting C-cadherin mediated cell adhesion. PRINCIPAL FINDINGS: We have investigated the functional and physical relationships between PAPC, FLRT3, and C-cadherin. Although neither PAPC nor FLRT3 are required for each other to regulate C-cadherin adhesion, they do interact functionally and physically, and they form a complex with cadherins. By itself PAPC reduces cell adhesion physiologically to induce cell sorting, while FLRT3 disrupts adhesion excessively to cause cell dissociation. However, when expressed together PAPC limits the cell dissociating and tissue disrupting activity of FLRT3 to make it effective in physiological cell sorting. PAPC counteracts FLRT3 function by inhibiting the recruitment of the GTPase RND1 to the FLRT3 cytoplasmic domain. CONCLUSIONS/SIGNIFICANCE: PAPC and FLRT3 form a functional complex with cadherins and PAPC functions as a molecular "governor" to maintain FLRT3 activity at the optimal level for physiological regulation of C-cadherin adhesion, cell sorting, and morphogenesis
Files in This Item:
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DOI
10.1371/journal.pone.0008411
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Biochemistry and Molecular Biology (생화학-분자생물학교실) > 1. Journal Papers
Yonsei Authors
Koh, Eun Jin(고은진) ORCID logo https://orcid.org/0000-0001-8967-6266
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/106059
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