Nuclear Notch1 signaling and the regulation of dendritic development (original) (raw)
References
Greenwald, I. & Rubin, G. M. Making a difference: the role of cell–cell interactions in establishing separate identities for equivalent cells. Cell68, 271–281 (1992). ArticleCAS Google Scholar
Ghysen, A., Dambly-Chaudiere, C., Jan, L. Y. & Jan, Y. N. Cell interactions and gene interactions in peripheral neurogenesis. Genes Dev.7, 723–733 ( 1993). ArticleCAS Google Scholar
Artavanis-Tsakonas, S., Matsuno, K. & Fortini, M. E. Notch signaling. Science268 , 225–232 (1995). ArticleCAS Google Scholar
Kimble, J. & Simpson, P. The lin-12/Notch signaling pathway and its regulation. Annu. Rev. Cell Dev. Biol.13, 333–361 (1997). ArticleCAS Google Scholar
Greenwald, I. Lin-12/Notch signaling: lessons from worms and flies. Genes Dev.12, 1751–1762 ( 1998). ArticleCAS Google Scholar
Pan, D. & Rubin, G. M. Kuzbanian controls proteolytic processing of Notch and mediates lateral inhibition during Drosophila and vertebrate neurogenesis. Cell90, 271 –280 (1997). ArticleCAS Google Scholar
Blaumueller, C. M., Qi, H., Zagouras, P. & Artavanis-Tsakonas, S. Intracellular cleavage of Notch leads to a heterodimeric receptor on the plasma membrane. Cell90, 281–291 (1997). ArticleCAS Google Scholar
Logeat, F. et al. The Notch1 receptor is cleaved constitutively by a furin-like convertase. Proc. Natl. Acad. Sci. USA95, 8108–8112 (1998). ArticleCAS Google Scholar
Kidd, S., Lieber, T. & Young, M. W. Ligand-induced cleavage and regulation of nuclear entry of Notch in Drosophila melanogaster embryos. Genes Dev.12, 3728–3740 ( 1998). ArticleCAS Google Scholar
Fortini, M. E. & Artavanis-Tsakonas, S. The suppressor of hairless protein participates in notch receptor signaling. Cell79, 273–282 ( 1994). ArticleCAS Google Scholar
Lecourtois, M. & Schweisguth, F. The neurogenic Suppressor of Hairless DNA-binding protein mediates the transcriptional activation of the Enhancer of split Complex genes triggered by Notch signaling. Genes Dev.9, 2598–2608 (1995). ArticleCAS Google Scholar
Jarriault, S. et al. Signalling downstream of activated mammalian Notch. Nature377, 355–358 ( 1995). ArticleCAS Google Scholar
Tamura, K. et al. Physical interaction between a novel domain of the receptor Notch and the transcription factor RBP-J kappa/Su(H). Curr. Biol.5, 1416–1423 (1995). ArticleCAS Google Scholar
Hsieh, J. J. et al. Truncated mammalian Notch1 activates CBF1/RBPJk-repressed genes by a mechanism resembling that of Epstein-Barr virus EBNA2. Mol. Cell. Biol.16, 952–959 (1996). ArticleCAS Google Scholar
Lu, F. M. & Lux, S. E. Constitutively active human Notch1 binds to the transcription factor CBF1 and stimulates transcription through a promoter containing a CBF1–responsive element. Proc. Natl. Acad. Sci. USA93, 5663–5667 (1996). ArticleCAS Google Scholar
Kopan, R., Schroeter, E. H., Weintraub, H. & Nye, J. S. Signal transduction by activated mNotch: importance of proteolytic processing and its regulation by the extracellular domain. Proc. Natl. Acad. Sci. USA93, 1683–1688 ( 1996). ArticleCAS Google Scholar
Struhl, G. & Adachi, A. Nuclear access and action of Notch in vivo. Cell93, 649– 660 (1998). ArticleCAS Google Scholar
Schroeter, E. H., Kisslinger, J. A. & Kopan, R. Notch1 signalling requires ligand-induced proteolytic release of intracellular domain. Nature393, 382–386 (1998). ArticleCAS Google Scholar
Lecourtois, M. & Schweisguth, F. Indirect evidence for Delta-dependent intracellular processing of Notch in Drosophila embryos. Curr. Biol.8, 771– 774 (1998). ArticleCAS Google Scholar
Coffman, C., Harris, W. & Kintner, C. Xotch, the Xenopus homolog of Drosophila notch. Science249, 1438– 1441 (1990). ArticleCAS Google Scholar
Coffman, C. R., Skoglund, P., Harris, W. A. & Kintner, C. R. Expression of an extracellular deletion of Xotch diverts cell fate in Xenopus embryos. Cell73, 659– 671 (1993). ArticleCAS Google Scholar
Chitnis, A., Henrique, D., Lewis, J., Ish-Horowicz, D. & Kintner, C. Primary neurogenesis in Xenopus embryos regulated by a homologue of the Drosophila neurogenic gene Delta. Nature375, 761–766 ( 1995). ArticleCAS Google Scholar
Dorsky, R. I., Rapaport, D. H. & Harris, W. A. Xotch inhibits cell differentiation in the Xenopus retina. Neuron14, 487– 496 (1995). ArticleCAS Google Scholar
Austin, C. P., Feldman, D. E., Ida, J. A. Jr. & Cepko, C. L. Vertebrate retinal ganglion cells are selected from competent progenitors by the action of Notch. Development121 , 3637–3650 (1995). CASPubMed Google Scholar
Weinmaster, G., Roberts, V. J. & Lemke, G. A homolog of Drosophila Notch expressed during mammalian development. Development113, 199–205 (1991). CASPubMed Google Scholar
del Amo, F. F. et al. Expression pattern of Motch, a mouse homologue of Drosophila Notch, suggests an important role in early postimplantation mouse development. Development115, 737– 744 (1992). CASPubMed Google Scholar
Reaume, A. G., Conlon, R. A., Zirngibl, R., Yamaguchi, T. P. & Rossant, J. Expression analysis of a Notch homologue in the mouse embryo. Dev. Biol.154, 377 –387 (1992). ArticleCAS Google Scholar
Weinmaster, G., Roberts, V. J. & Lemke, G. Notch2: a second mammalian Notch gene. Development116, 931–941 ( 1992). CASPubMed Google Scholar
Lardelli, M., Dahlstrand, J. & Lendahl, U. The novel Notch homologue mouse Notch3 lacks specific epidermal growth factor-repeats and is expressed in proliferating neuroepithelium. Mech. Dev.46, 123–136 (1994). ArticleCAS Google Scholar
Lindsell, C. E., Boulter, J., diSibio, G., Gossler, A. & Weinmaster, G. Expression patterns of Jagged, Delta1, Notch1, Notch2, and Notch3 genes identify ligand-receptor pairs that may function in neural development. Mol. Cell. Neurosci.8, 14– 27 (1996). ArticleCAS Google Scholar
Bettenhausen, B., de Angelis, M. H., Simon, D., Guenet, J. L. & Gossler, A. Transient and restricted expression during mouse embryogenesis of _Dll_1, a murine gene closely related to Drosophila Delta. Development121, 2407–2418 (1995). CASPubMed Google Scholar
Lindsell, C. E., Shawber, C. J., Boulter, J. & Weinmaster, G. Jagged: a mammalian ligand that activates Notch1. Cell80, 909–917 (1995). ArticleCAS Google Scholar
Shawber, C., Boulter, J., Lindsell, C. E. & Weinmaster, G. Jagged2: a serrate-like gene expressed during rat embryogenesis. Dev. Biol.180, 370–376 (1996). ArticleCAS Google Scholar
Swiatek, P. J., Lindsell, C. E., del Amo, F. F., Weinmaster, G. & Gridley, T. Notch1 is essential for postimplantation development in mice. Genes Dev.8, 707– 719 (1994). ArticleCAS Google Scholar
Conlon, R. A., Reaume, A. G. & Rossant, J. Notch1 is required for the coordinate segmentation of somites. Development121, 1533– 1545 (1995). CASPubMed Google Scholar
Lardelli, M., Williams, R., Mitsiadis, T. & Lendahl, U. Expression of the Notch 3 intracellular domain in mouse central nervous system progenitor cells is lethal and leads to disturbed neural tube development. Mech. Dev.59, 177–190 (1996). ArticleCAS Google Scholar
Chenn, A. & McConnell, S. K. Cleavage orientation and the asymmetric inheritance of Notch 1 immunoreactivity in mammalian neurogenesis. Cell82, 631–641 (1995). ArticleCAS Google Scholar
Gonatas, J. O., Gonatas, M. K., Stieber, A. & Fleischer, B. Isolation and characterization of an enriched Golgi fraction from neurons of developing rat brains. J. Neurochem.45, 497–507 (1985). ArticleCAS Google Scholar
Rebay, I., Fehon, R. G. & Artavanis-Tsakonas, S. Specific truncations of Drosophila Notch define dominant activated and dominant negative forms of the receptor. Cell74, 319–329 (1993). ArticleCAS Google Scholar
Schmechel, D. E., Brightman, M. W. & Marangos, P. J. Neurons switch from non-neuronal enolase to neuron-specific enolase during differentiation. Brain Res.190, 195–214 (1980). ArticleCAS Google Scholar
Forss-Petter, S. et al. Transgenic mice expressing β-galactosidase in mature neurons under neuron-specific enolase promoter control. Neuron5, 187–197 ( 1990). ArticleCAS Google Scholar
Shawber, C. et al. Notch signaling inhibits muscle cell differentiation through a CBF1–independent pathway. Development122, 3765–3773 (1996). CASPubMed Google Scholar
Qi, H. et al. Processing of the Notch ligand Delta by the metalloprotease Kuzbanian. Science283, 91–94 (1999). ArticleCAS Google Scholar
Berezovska, O. et al. Notch1 inhibits neurite outgrowth in postmitotic primary neurons. Neuroscience93, 433– 439 (1999). ArticleCAS Google Scholar
Sestan, N., Artavanis-Tsakonas, A. & Rakic, P. Contact-dependent inhibition of cortical neurite growth mediated by Notch signaling. Science286, 741–746 (1999). ArticleCAS Google Scholar
Giniger, E., Jan, L. Y. & Jan, Y.-N. Specifying the path of the intersegmental nerve of the Drosophila embryo: a role for Delta and Notch. Development117, 431–440 ( 1993). CASPubMed Google Scholar
Fambrough, D., Pan, D., Rubin, G. M. & Goodman, C. S. The cell surface metalloprotease/disintegrin Kuzbanian is required for axonal extension in Drosophila. Proc. Natl. Acad. Sci. USA93, 13233–13238 (1996). ArticleCAS Google Scholar
Threadgill, R., Bobb, K. & Ghosh, A. Regulation of dendritic growth and remodeling by Rho, Rac, and Cdc42. Neuron19, 625–634 ( 1997). ArticleCAS Google Scholar
Thormodsson, F. R., Redmond, L. & Hockfield, S. Identification of nuclear proteins that are developmentally regulated in embryonic rat brain. J. Neurochem.64, 1919–1927 (1995). ArticleCAS Google Scholar