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Development, Vol 116, Issue 4 931-941, Copyright © 1992 by Company of Biologists


JOURNAL ARTICLES

Notch2: a second mammalian Notch gene

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

Notch is a cell surface receptor that mediates a wide variety of cellular interactions that specify cell fate during Drosophila development. Recently, homologs of Drosophila Notch have been isolated from Xenopus, human and rat, and the expression patterns of these vertebrate proteins suggest that they may be functionally analogous to their Drosophila counterpart. We have now identified a second rat gene that exhibits substantial nucleic and amino acid sequence identity to Drosophila Notch. This gene, designated Notch2, encodes a protein that contains all the structural motifs characteristic of a Notch protein. Thus, mammals differ from Drosophila in having more than one Notch gene. Northern and in situ hybridisation analyses in the developing and adult rat identify distinct spatial and temporal patterns of expression for Notch1 and Notch2, indicating that these genes are not redundant. These results suggest that the great diversity of cell-fate decisions regulated by Notch in Drosophila may be further expanded in vertebrates by the activation of distinct Notch proteins.
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Development, January 5, 1997; 124(10): 1887 - 1897.
[Abstract] [PDF]


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DevelopmentHome page
T. Mitsiadis, D Henrique, I Thesleff, and U Lendahl
Mouse Serrate-1 (Jagged-1): expression in the developing tooth is regulated by epithelial-mesenchymal interactions and fibroblast growth factor-4
Development, January 4, 1997; 124(8): 1473 - 1483.
[Abstract] [PDF]


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DevelopmentHome page
J. de la Pompa, A Wakeham, K. Correia, E Samper, S Brown, R. Aguilera, T Nakano, T Honjo, T. Mak, J Rossant, et al.
Conservation of the Notch signalling pathway in mammalian neurogenesis
Development, January 3, 1997; 124(6): 1139 - 1148.
[Abstract] [PDF]


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J. Neurosci.Home page
M. K. Lee, H. H. Slunt, L. J. Martin, G. Thinakaran, G. Kim, S. E. Gandy, M. Seeger, E. Koo, D. L. Price, and S. S. Sisodia
Expression of Presenilin 1 and 2 (PS1 and PS2) in Human and Murine Tissues
J. Neurosci., December 1, 1996; 16(23): 7513 - 7525.
[Abstract] [Full Text] [PDF]


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Proc. Natl. Acad. Sci. USAHome page
L. A. Milner, A. Bigas, R. Kopan, C. Brashem-Stein, I. D. Bernstein, and D. I. K. Martin
Inhibition of granulocytic differentiation by mNotch1
PNAS, November 12, 1996; 93(23): 13014 - 13019.
[Abstract] [Full Text] [PDF]


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Genes Dev.Home page
L Girard, Z Hanna, N Beaulieu, C D Hoemann, C Simard, C A Kozak, and P Jolicoeur
Frequent provirus insertional mutagenesis of Notch1 in thymomas of MMTVD/myc transgenic mice suggests a collaboration of c-myc and Notch1 for oncogenesis.
Genes & Dev., August 1, 1996; 10(15): 1930 - 1944.
[Abstract] [PDF]


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DevelopmentHome page
H Uyttendaele, G Marazzi, G Wu, Q Yan, D Sassoon, and J Kitajewski
Notch4/int-3, a mammary proto-oncogene, is an endothelial cell-specific mammalian Notch gene
Development, July 1, 1996; 122(7): 2251 - 2259.
[Abstract] [PDF]


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DevelopmentHome page
C Shawber, D Nofziger, J. Hsieh, C Lindsell, O Bogler, D Hayward, and G Weinmaster
Notch signaling inhibits muscle cell differentiation through a CBF1-independent pathway
Development, January 12, 1996; 122(12): 3765 - 3773.
[Abstract] [PDF]


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DevelopmentHome page
D. Raible and J. Eisen
Regulative interactions in zebrafish neural crest
Development, January 2, 1996; 122(2): 501 - 507.
[Abstract] [PDF]


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ScienceHome page
S Artavanis-Tsakonas, K Matsuno, and M. Fortini
Notch signaling
Science, April 14, 1995; 268(5208): 225 - 232.
[Abstract] [PDF]


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DevelopmentHome page
C. Austin, D. Feldman, J. Ida, and C. Cepko
Vertebrate retinal ganglion cells are selected from competent progenitors by the action of Notch
Development, January 11, 1995; 121(11): 3637 - 3650.
[Abstract] [PDF]


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DevelopmentHome page
C Oka, T Nakano, A Wakeham, J. de la Pompa, C Mori, T Sakai, S Okazaki, M Kawaichi, K Shiota, T. Mak, et al.
Disruption of the mouse RBP-J kappa gene results in early embryonic death
Development, January 10, 1995; 121(10): 3291 - 3301.
[Abstract] [PDF]


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DevelopmentHome page
B Bettenhausen, M Hrabe de Angelis, D Simon, J. Guenet, and A Gossler
Transient and restricted expression during mouse embryogenesis of Dll1, a murine gene closely related to Drosophila Delta
Development, January 8, 1995; 121(8): 2407 - 2418.
[Abstract] [PDF]


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DevelopmentHome page
R. Conlon, A. Reaume, and J Rossant
Notch1 is required for the coordinate segmentation of somites
Development, January 5, 1995; 121(5): 1533 - 1545.
[Abstract] [PDF]


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DevelopmentHome page
A. Newman, J. White, and P. Sternberg
The Caenorhabditis elegans lin-12 gene mediates induction of ventral uterine specialization by the anchor cell
Development, January 2, 1995; 121(2): 263 - 271.
[Abstract] [PDF]


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DevelopmentHome page
R. Kopan, J. S. Nye, and H. Weintraub
The intracellular domain of mouse Notch: a constitutively activated repressor of myogenesis directed at the basic helix-loop-helix region of MyoD
Development, September 1, 1994; 120(9): 2385 - 2396.
[Abstract] [PDF]


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DevelopmentHome page
J. S. Nye, R. Kopan, and R. Axel
An activated Notch suppresses neurogenesis and myogenesis but not gliogenesis in mammalian cells
Development, September 1, 1994; 120(9): 2421 - 2430.
[Abstract] [PDF]


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Genes Dev.Home page
P J Swiatek, C E Lindsell, F F del Amo, G Weinmaster, and T Gridley
Notch1 is essential for postimplantation development in mice.
Genes & Dev., March 15, 1994; 8(6): 707 - 719.
[Abstract] [PDF]


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DevelopmentHome page
R. Diederich, K Matsuno, H Hing, and S Artavanis-Tsakonas
Cytosolic interaction between deltex and Notch ankyrin repeats implicates deltex in the Notch signaling pathway
Development, January 3, 1994; 120(3): 473 - 481.
[Abstract] [PDF]


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Cold Spring Harb Symp Quant BiolHome page
J. Aster, W. Pear, R. Hasserjian, H. Erba, F. Davi, B. Luo, M. Scott, D. Baltimore, and J. Sklar
Functional Analysis of the TAN-1 Gene, a Human Homolog of Drosophila Notch
Cold Spring Harb Symp Quant Biol, January 1, 1994; 59(0): 125 - 136.
[Abstract] [PDF]


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DevelopmentHome page
K. Fitzgerald, H. A. Wilkinson, and I. Greenwald
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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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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J. Biol. Chem.Home page
J. Ingles-Esteve, L. Espinosa, L. A. Milner, C. Caelles, and A. Bigas
Phosphorylation of Ser2078 Modulates the Notch2 Function in 32D Cell Differentiation
J. Biol. Chem., November 21, 2001; 276(48): 44873 - 44880.
[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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