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PMID: 7716513 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Notch signaling.

Science (New York, N.Y.) ·Vol. 268 ·No. 5208 ·1995-04-14 ·Pages 225-32

Artavanis-Tsakonas S, Matsuno K, Fortini ME

Abstract

The Notch/Lin-12/Glp-1 receptor family mediates the specification of numerous cell fates during development in Drosophila and Caenorhabditis elegans. Studies on the expression, mutant phenotypes, and developmental consequences of unregulated receptor activation have implicated these proteins in a general mechanism of local cell signaling, which includes interactions between equivalent cells and between different cell types. Genetic approaches in flies and worms have identified putative components of the signaling cascade, including a conserved family of extracellular ligands and two cellular factors that may associate with the Notch Intracellular domain. One factor, the Drosophila Suppressor of Hairless protein, is a DNA-binding protein, which suggests that Notch signaling may involve relatively direct signal transmission from the cell surface to the nucleus. Several vertebrate Notch receptors have also been discovered recently and play important roles in normal development and tumorigenesis.

MeSH Terms
Animals Caenorhabditis elegans/genetics,physiology Caenorhabditis elegans Proteins Cell Differentiation Drosophila Proteins Drosophila melanogaster/genetics,physiology Helminth Proteins/physiology Humans Ligands Membrane Glycoproteins/physiology Membrane Proteins/genetics,physiology Neoplasms/metabolism Nuclear Proteins/metabolism Receptors, Cell Surface/genetics,physiology Receptors, Notch Signal Transduction
Chemicals
Caenorhabditis elegans Proteins Drosophila Proteins Glp-1 protein, C elegans Helminth Proteins Ligands Lin-12 protein, C elegans Membrane Glycoproteins Membrane Proteins N protein, Drosophila Nuclear Proteins Receptors, Cell Surface Receptors, Notch
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Artavanis-Tsakonas S
Howard Hughes Medical Institute, Boyer Center for Molecular Medicine, Yale University, New Haven, CT 06536, USA.
Matsuno K
Fortini M E
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1995-04-14
Pages
225-32
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NINDS NIH HHS · NS26084 · United States
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