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Development, Vol 113, Issue 1 199-205, Copyright © 1991 by Company of Biologists


JOURNAL ARTICLES

A homolog of Drosophila Notch expressed during mammalian development

G Weinmaster, VJ Roberts and G Lemke
Molecular Neurobiology Laboratory, Salk Institute, San Diego, CA 92186.

Drosophila Notch and the related Caenorhabditis elegans proteins lin-12 and glp-1 function as mediators of local cell-cell interactions required for cell-fate decisions during invertebrate development. To investigate the possibility that similar proteins play determinative roles during mammalian development, we isolated cDNA clones encoding rat Notch. The deduced amino acid sequence of this protein contains 36 epidermal growth factor (EGF)-like repeats, and is remarkably similar in both its extracellular and cytoplasmic domains to the sequence of Xenopus Xotch and Drosophila Notch. In the developing central nervous system, in situ hybridisation analyses revealed that Notch transcripts were dramatically restricted to the ventricular proliferative zones of embryonic neuroepithelia. Notch was also strongly expressed during development of non-neural tissues, such as hair follicles and tooth buds, whose correct differentiation requires epithelial-mesenchymal interactions. These data support the hypothesis that Notch plays an essential role in mammalian development and pattern formation that closely parallels its role in the development of invertebrates.
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glp-1 can substitute for lin-12 in specifying cell fate decisions in Caenorhabditis elegans
Development, December 1, 1993; 119(4): 1019 - 1027.
[Abstract] [PDF]


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Genes Dev.Home page
T Lieber, S Kidd, E Alcamo, V Corbin, and M W Young
Antineurogenic phenotypes induced by truncated Notch proteins indicate a role in signal transduction and may point to a novel function for Notch in nuclei.
Genes & Dev., October 1, 1993; 7(10): 1949 - 1965.
[Abstract] [PDF]


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DevelopmentHome page
P Heitzler and P Simpson
Altered epidermal growth factor-like sequences provide evidence for a role of Notch as a receptor in cell fate decisions
Development, January 3, 1993; 117(3): 1113 - 1123.
[Abstract] [PDF]


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DevelopmentHome page
G. Weinmaster, V. J. Roberts, and G. Lemke
Notch2: a second mammalian Notch gene
Development, December 1, 1992; 116(4): 931 - 941.
[Abstract] [PDF]


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DevelopmentHome page
F. Del Amo, D. Smith, P. Swiatek, M Gendron-Maguire, R. Greenspan, A. McMahon, and T Gridley
Expression pattern of Motch, a mouse homolog of Drosophila Notch, suggests an important role in early postimplantation mouse development
Development, January 7, 1992; 115(3): 737 - 744.
[Abstract] [PDF]


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Cold Spring Harb Symp Quant BiolHome page
P. Simpson, M. Bourouis, P. Heitzler, L. Ruel, M. Haenlin, and P. Ramain
Delta, Notch, and shaggy: Elements of a Lateral Signaling Pathway in Drosophila
Cold Spring Harb Symp Quant Biol, January 1, 1992; 57(0): 391 - 400.
[Abstract] [PDF]


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Cold Spring Harb Symp Quant BiolHome page
J. Kimble, S. Crittenden, E. Lambie, V. Kodoyianni, S. Mango, and E. Troemel
Regulation of Induction by GLP1, a Localized Cell Surface Receptor in Caenorhabditis elegans
Cold Spring Harb Symp Quant Biol, January 1, 1992; 57(0): 401 - 407.
[Abstract] [PDF]


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J. Biol. Chem.Home page
K. Shimizu, S. Chiba, T. Saito, K. Kumano, T. Takahashi, and H. Hirai
Manic Fringe and Lunatic Fringe Modify Different Sites of the Notch2 Extracellular Region, Resulting in Different Signaling Modulation
J. Biol. Chem., July 6, 2001; 276(28): 25753 - 25758.
[Abstract] [Full Text] [PDF]


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Proc. Natl. Acad. Sci. USAHome page
T. Mizutani, Y. Taniguchi, T. Aoki, N. Hashimoto, and T. Honjo
Conservation of the biochemical mechanisms of signal transduction among mammalian Notch family members
PNAS, July 31, 2001; 98(16): 9026 - 9031.
[Abstract] [Full Text] [PDF]




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