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PMID: 11489213 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Selective control of basolateral membrane protein polarity by cdc42.

Traffic (Copenhagen, Denmark) ·Vol. 2 ·No. 8 ·2001-08-00 ·Pages 556-64

Cohen D, Müsch A, Rodriguez-Boulan E

Abstract

The rho GTPase cdc42 is implicated in several aspects of cell polarity. A recent study (Kroschewski R, Hall A, Mellman I. Nat Cell Biol 1999;1:8-13) demonstrated that a dominant negative mutant of cdc42 abolishes the polarity of basolateral membrane proteins in MDCK cells, but did not elucidate whether this effect was selective for basolateral proteins or nonselective for all secreted proteins. To answer this question, we analyzed the polarity of newly synthesized membrane and soluble proteins in MDCK cell lines previously induced to overexpress mutant forms of cdc42. GTPase-deficient and dominant negative cdc42 did not affect the apical targeting of a newly synthesized apical membrane protein, but reversed to apical the distribution of two exogenous basolateral membrane proteins. In striking contrast, GTPase-deficient cdc42 did not affect polarized exocytosis of endogenous soluble proteins, either apical or basolateral. The exquisitely selective regulation of polarized protein targeting by cdc42 may allow cells to fine-tune their membrane composition in response to extracellular signals during development, migration and in response to injury.

MeSH Terms
Adenosine Triphosphatases/metabolism Animals Blotting, Western Cation Transport Proteins Cell Line Cell Membrane/metabolism Cell Movement Dogs Fluorescent Antibody Technique, Indirect GTP Phosphohydrolases/metabolism Genes, Dominant Humans Mutation Protein Binding Protein Structure, Tertiary Protein Synthesis Inhibitors/pharmacology Signal Transduction Tetracycline/pharmacology cdc42 GTP-Binding Protein/genetics,metabolism,physiology
Chemicals
Cation Transport Proteins Protein Synthesis Inhibitors Adenosine Triphosphatases GTP Phosphohydrolases sodium-translocating ATPase cdc42 GTP-Binding Protein Tetracycline
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Cohen D
Dyson Institute of Vision Research, Department of Biochemistry, Joan and Sanford Weill Medical College of Cornell University, New York, New York, 10021, USA.
Müsch A
Rodriguez-Boulan E
Article Info
Journal
Traffic (Copenhagen, Denmark)
Abbr.
Traffic
ISSN
1398-9219
Published
2001-08-00
Pages
556-64
Language
English
Region
England
NLM ID
100939340
Subset
IM
Grants
NIGMS NIH HHS · R01 GM034107 · United States
CGH CDC HHS · GH34107 · United States
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