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PMID: 8573338 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Tight junctions, membrane-associated guanylate kinases and cell signaling.

Current opinion in cell biology ·Vol. 7 ·No. 5 ·1995-10-00 ·Pages 641-9

Kim SK

Abstract

Proteins that define a new family, termed membrane-associated guanylate kinases, have recently been identified as structural components of epithelial tight junctions and neuronal synapses, and as cell signaling proteins in Drosophila and Caenorhabditis elegans. In particular, the lin-2 gene has been shown to encode a membrane-associated guanylate kinase and to act in the let-23 receptor tyrosine kinase/let-60 ras signaling pathway that controls vulval induction in C. elegans. The combined data from recent biochemical and genetic analyses of membrane-associated guanylate kinases suggest that certain tight junction proteins can play an important role in cell signaling pathways. One possibility is that asymmetric segregation of signaling receptors to the basolateral membrane domain of polarized epithelial cells is crucial for proper cell signaling, and that membrane-associated guanylate kinases may be required for this localization.

MeSH Terms
Animals Guanylate Kinases Nucleoside-Phosphate Kinase/physiology Signal Transduction/physiology Synapses/physiology,ultrastructure Tight Junctions/physiology,ultrastructure
Chemicals
Nucleoside-Phosphate Kinase Guanylate Kinases
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Kim S K
Department of Developmental Biology, Stanford University Medical School, CA 94305, USA.
Article Info
Journal
Current opinion in cell biology
Abbr.
Curr Opin Cell Biol
ISSN
0955-0674
Published
1995-10-00
Pages
641-9
Language
English
Region
England
NLM ID
8913428
Subset
IM
Corrections
ErratumIn
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