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PMID: 9547311 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Contributions of extracellular and intracellular domains of full length and chimeric cadherin molecules to junction assembly in epithelial cells.

Journal of cell science ·Vol. 111 ( Pt 9) ·1998-05-00 ·Pages 1305-18

Norvell SM, Green KJ

Abstract

The integrity of cell-cell junctions in epithelial cells depends on functional interactions of both extracellular and intracellular domains of cadherins with other junction proteins. To examine the roles of the different domains of E-cadherin and desmoglein in epithelial junctions, we stably expressed full length desmoglein 1 and chimeras of E-cadherin and desmoglein 1 in A431 epithelial cells. Full length desmoglein 1 was able to incorporate into or disrupt endogenous desmosomes depending on expression level. Each of the chimeric cadherin molecules exhibited distinct localization patterns at the cell surface. A chimera of the desmoglein 1 extracellular domain and the E-cadherin intracellular domain was distributed diffusely at the cell surface while the reverse chimera, comprising the E-cadherin extracellular domain and the desmoglein 1 intracellular domain, localized in large, sometimes contiguous patches at cell-cell interfaces. Nevertheless, both constructs disrupted desmosome assembly. Expression of constructs containing the desmoglein 1 cytoplasmic domain resulted in approximately a 3-fold decrease in E-cadherin bound to plakoglobin and a 5- to 10-fold reduction in the steady-state levels of the endogenous desmosomal cadherins, desmoglein 2 and desmocollin 2, possibly contributing to the dominant negative effect of the desmoglein 1 tail. In addition, biochemical analysis of protein complexes in the stable lines revealed novel in vivo protein interactions. Complexes containing beta-catenin and desmoglein 1 were identified in cells expressing constructs containing the desmoglein 1 tail. Furthermore, interactions were identified between endogenous E-cadherin and the chimera containing the E-cadherin extracellular domain and the desmoglein 1 intracellular domain providing in vivo evidence for previously predicted lateral interactions of E-cadherin extracellular domains.

MeSH Terms
Cadherins/chemistry,genetics,metabolism Carcinoma, Squamous Cell/pathology Cytoskeletal Proteins/metabolism DNA, Complementary/genetics Desmocollins Desmoglein 1 Desmoglein 2 Desmogleins Desmoplakins Desmosomes/chemistry,ultrastructure Macromolecular Substances Protein Binding Protein Structure, Tertiary Recombinant Fusion Proteins/chemistry,metabolism Solubility Structure-Activity Relationship Transfection Tumor Cells, Cultured gamma Catenin
Chemicals
Cadherins Cytoskeletal Proteins DNA, Complementary Desmocollins Desmoglein 1 Desmoglein 2 Desmogleins Desmoplakins Macromolecular Substances Recombinant Fusion Proteins gamma Catenin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Norvell S M
Department of Pathology, Northwestern University Medical School, Chicago, IL 60611, USA.
Green K J
Article Info
Journal
Journal of cell science
Abbr.
J Cell Sci
ISSN
0021-9533
Published
1998-05-00
Pages
1305-18
Language
English
Region
England
NLM ID
0052457
Subset
IM
Grants
NIDCR NIH HHS · P01 DE12328 · United States
NIAMS NIH HHS · R01 AR41836 · United States
NIEHS NIH HHS · T32ES07284 · United States
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