Epsin potentiates Notch pathway activity in Drosophila and C. elegans

Development

Volumn 131, Issue 23, 2004, Pages 5807-5815

  Tian, Xiaolin ^a   Hansen, Dave ^a,b   Schedl, Tim ^a   Skeath, James B ^a  

^a WASHINGTON UNIVERSITY   (United States)

^b UNIVERSITY OF CALGARY   (Canada)

Author keywords

C. elegans Drosophila; Epsins; Notch

Indexed keywords

EPSIN; NOTCH RECEPTOR;

ARTICLE; DROSOPHILA; GENE INTERACTION; GENETIC CONSERVATION; GENETIC SCREENING; GERM CELL; GROWTH INHIBITION; HEART DEVELOPMENT; MUTANT; MYOBLAST; NONHUMAN; ORTHOLOGY; PHENOTYPIC VARIATION; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN TARGETING; SIGNAL TRANSDUCTION;

ADAPTOR PROTEINS, VESICULAR TRANSPORT; ANIMALS; CAENORHABDITIS ELEGANS; CLONING, MOLECULAR; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; ENDOCYTOSIS; EVOLUTION, MOLECULAR; GERM-LINE MUTATION; IMMUNOHISTOCHEMISTRY; LIGANDS; MEMBRANE PROTEINS; MICE; MICROSCOPY, FLUORESCENCE; MUSCLES; MUTATION; MYOCARDIUM; PHENOTYPE; RECEPTORS, NOTCH; RNA INTERFERENCE; SIGNAL TRANSDUCTION; SPECIES SPECIFICITY; TRANSGENES; VESICULAR TRANSPORT PROTEINS;

ANIMALIA;

EID: 12344309339     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: 10.1242/dev.01459     Document Type: Article

References (61)

1. Aguilar, R. C., Watson, H. A. and Wendland, B. (2003). The yeast Epsin Ent1 is recruited to membranes through multiple independent interactions. J. Biol. Chem. 278, 10737-10743.
2. Austin, J. and Kimble, J. (1987). glp-1 is required in the germ line for regulation of the decision between mitosis and meiosis in C. elegans. Cell 51, 589-599.
3. Austin, J. and Kimble, J. (1989). Transcript analysis of glp-1 and lin-12, homologous genes required for cell interactions during development of C. elegans. Cell 58, 565-571.
4. Bate, M. (1993). The mesoderm and its derivatives. In The Development of Drosophila melanogaster, Vol. 2 (ed. M. Bate and A. Martinez-Arias), pp. 1023-1090. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press.
5. Baylies, M. K., Bate, M. and Ruiz Gomez, M. (1998). Myogenesis: a view from Drosophila. Cell 93, 921-927.
6. Berry, L., Westlund, B. and Schedl, T. (1997). Germline tumor formation caused by activation of glp-1, a member of the Notch family of receptors. Development 124, 925-936.
7. Bodmer, R. and Frasch, M. (1999). Genetic Determination of Drosophila heart development. In Heart Development (ed. R. P. Harvey and N. Rosenthal), pp. 65-90. San Diego, CA: Academic Press.
8. Cadavid, A. L., Ginzel, A. and Fischer, J. A. (2000). The function of the Drosophila fat facets deubiquitinating enzyme in limiting photoreceptor cell number is intimately associated with endocytosis. Development 127, 1727-1736.
9. Carmena, A., Bate, M. and Jimenez, F. (1995). lethal of scute, a proneural gene, participates in the specification of muscle progenitors during Drosophila embryogenesis. Genes Dev. 9, 2372-2383.
10. Chen, H., Fre, S., Slepnev, V. I., Capua, M. R., Takei, K., Butler, M. H., di Fiore, P. P. and de Camilli, P. (1998). Epsin is an EH-domain-binding protein implicated in clathrin-mediated endocytosis. Nature 394, 793-797.
11. Corbin, V., Michelson, A. M., Abmayr, S. M., Neel, V., Alcomo, E., Maniatis, T. and Young, M. W. (1991). A role for the Drosophila neurogenic genes in mesoderm differentiation. Cell 67, 311-323.
12. Crittenden, S. L., Troemel, E. R., Evans, T. C. and Kimble, J. (1994). GLP-1 is localized to the mitotic region of the C. elegans germ line. Development 120, 2901-2911.
13. De Camilli, P., Chen, H., Hyman, J., Panepucci, E., Bateman, A. and Brunger, A. T. (2002). The ENTH domain. FEBS Lett. 513, 11-18.
14. Deblandre, G. A., Lai, E. C. and Kintner, C. (2001). Xenopus neuralized is a ubiquitin ligase that interacts with XDelta1 and regulates Notch signaling. Dev. Cell 1, 795-806.
15. Duan, H., Skeath, J. B. and Nguyen, H. T. (2001). Drosophila Lame duck, a novel member of the Gli superfamily, acts as a key regulator of myogenesis by controlling fusion-competent myoblast development. Development 128, 4489-4500.
16. Entchev, E. V., Schwabedissen, A. and Gonzalez-Gaitan, M. (2000). Gradient formation of the TGF-beta homolog Dpp. Cell 103, 981-991.
17. Fire, A., Xu, S., Montgomery, M. K., Kostas, S. A., Driver, S. E. and Mello, C. C. (1998). Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans. Nature 391, 806-811.
18. Fitzgerald, K. and Greenwald, I. (1995). Interchangeability of Caenorhabditis elegans DSL proteins and intrinsic signalling activity of their extracellular domains in vivo. Development 121, 4275-4282.
19. Frasch, M., Hoey, T., Rushlow, C., Doyle, H. and Levine, M. (1987). Characterization and localization of the even-skipped protein of Drosophila. EMBO J. 6, 749-759.
20. Giebel, B. (1999). The Notch signaling pathway is required to specify muscle progenitor cells in Drosophila. Mech. Dev. 86, 137-145.
21. Gonzalez-Gaitan, M. and Stenmark, H. (2003). Endocytosis and signaling: a relationship under development. Cell 115, 513-521.
22. Han, Z. and Bodmer, R. (2003). Myogenic cells fates are antagonized by Notch only in asymmetric lineages of the Drosophila heart, with or without cell division. Development 130, 3039-3051.
23. Hansen, D., Hubbard, E. J. and Schedl, T. (2004). Multi-pathway control of the proliferation versus meiotic development decision in the Caenorhabditis elegans germline. Dev. Biol. 268 342-357.
24. Hartenstein A. Y., Rugendorff, A., Tepass, U. and Hartenstein, V. (1992). The function of the neurogenic genes during epithelial development in the Drosophila embryo. Development 116 1203-1220.
25. Henderson, S. T., Gao, D., Lambie, E. J. and Kimble, J. (1994). lag-2 may encode a signaling ligand for the GLP-1 and LIN- 12 receptors of C. elegans. Development 120, 2913-2924.
26. Hicks, C., Ladi, E., Lindsell, C., Hsieh, J. J., Hayward, S. D., Collazo, A. and Weinmaster, G. (2002). A secreted Delta1-Fc fusion protein functions both as an activator and inhibitor of Notch1 signaling. J. Neurosci. Res. 68, 655-667.
27. Hukriede, N. A. and Fleming, R. J. (1997). Beaded of Goldschmidt, an antimorphic allele of Serrate, encodes a protein lacking transmembrane and intracellular domains. Genetics 145, 359-374.
28. Hukriede, N. A., Go, Y. and Fleming, R. J. (1997). A dominant-negative form of Serrate acts as a general antagonist of Notch activation. Development 124, 3427-3437.
29. Itoh, M., Kim, C. H., Palardy, G., Oda, T., Jiang, Y. J., Maust, D., Yeo, S. Y., Lorick, K., Wright, G. J., Ariza-McNaughton, L. et al. (2003). Mind bomb is a ubiquitin ligase that is essential for efficient activation of Notch signaling by Delta. Dev. Cell 4 67-82.
30. Itoh, T., Koshiba, S., Kigawa, T., Kikuchi, A., Yokoyama, S. and Takenawa, T. (2001). Role of the ENTH domain in phosphatidylinositol-4,5-bisphosphate binding and endocytosis. Science 291, 1047-1051.
31. Jones, A. R., Francis, R. and Schedl, T. (1996). GLD-1, a cytoplasmic protein essential for oocyte differentiation, shows stage- and sex-specific expression during Caenorhabditis elegans germline development. Dev. Biol. 180, 165-183.
32. Kay, B. K., Yamabhai, M., Wendland, B. and Emr, S. D. (1999). Identification of a novel domain shared by putative components of the endocytic and cytoskeletal machinery. Protein Sci. 8, 435-438.
33. Kodoyianni, V., Maine, E. M. and Kimble, J. (1992). Molecular basis of loss-of-function mutations in the glp-1 gene of Caenorhabditis elegans. Mol. Biol. Cell 3, 1199-1213.
34. Lai, E. C., Deblandre, G. A., Kintner, C. and Rubin, G. M. (2001). Drosophila neuralized is a ubiquitin ligase that promotes the internalization and degradation of delta. Dev. Cell 1, 783-794.
35. Lambie, E. J. and Kimble, J. (1991). Two homologous regulatory genes, lin-12 and glp-1, have overlapping functions. Development 112, 231-240.
36. Lilly, B., Zhao, B., Ranganayakulu, G., Paterson, B. M., Schutz, R. A. and Olson, E. N. (1995). Requirement of MADS domain transcription factor D-MEF2 for muscle formation in Drosophila. Science 267, 688-693.
37. Mumm, J. S. and Kopan, R. (2000). Notch signaling: from the outside in. Dev. Biol. 228, 151-165.
38. Overstreet, E., Chen, X., Wendland, B. and Fischer, J. A. (2003). Either part of a Drosophila epsin protein, divided after the ENTH domain, functions in endocytosis of delta in the developing eye. Curr. Biol. 13, 854-860.
39. Overstreet, E., Fitch, E. and Fischer, J. A. (2004). Fat facets and Liquid facets promote Delta endocytosis and Delta signaling in the signaling cells. Development 131, 5355-5366.
40. Parks, A. L., Klueg, K. M., Stout, J. R. and Muskavitch, M. A. (2000). Ligand endocytosis drives receptor dissociation and activation in the Notch pathway. Development 127, 1373-1385.
41. Pasierbek, P., Jantsch, M., Melcher, M., Schleiffer, A., Schweizer, D. and Loidl, J. (2001). A Caenorhabditis elegans cohesion protein with functions in meiotic chromosome pairing and disjunction. Genes Dev. 15, 1349-1360.
42. Pavlopoulos, E., Pitsouli, C., Klueg, K. M., Muskavitch, M. A., Moschonas, N. K. and Delidakis, C. (2001). neuralized Encodes a peripheral membrane protein involved in delta signaling and endocytosis. Dev. Cell 1, 807-816.
43. Pepper, A. S., Killian, D. J. and Hubbard, E. J. (2003). Genetic analysis of Caenorhabditis elegans glp-1 mutants suggests receptor interaction or competition. Genetics 163, 115-132.
44. Piddini, E. and Vincent, J. P. (2003). Modulation of developmental signals by endocytosis: different means and many ends. Curr. Opin. Cell Biol. 15, 474-481.
45. Priess, J. R., Schnabel, H. and Schnabel, R. (1987). The glp-1 locus and cellular interactions in early C. elegans embryos. Cell 51, 601-611.
46. Rosenthal, J. A., Chen, H., Slepnev, V. I., Pellegrini, L., Salcini, A. E., di Fiore, P. P. and de Camilli, P. (1999). The epsins define a family of proteins that interact with components of the clathrin coat and contain a new protein module. J. Biol. Chem. 274, 33959-33965.
47. Seto, E. S., Bellen, H. J. and Lloyd, T. E. (2002). When cell biology meets development: endocytic regulation of signaling pathways. Genes Dev. 16, 1314-1336.
48. Seugnet, L., Simpson, P. and Haenlin, M. (1997). Requirement for dynamin during Notch signaling in Drosophila neurogenesis. Dev. Biol. 192, 585-598.
49. Seydoux, G. and Schedl, T. (2001). The germline in C. elegans: origins. proliferation, and silencing. Int. Rev. Cytol. 203, 139-185.
50. Shih, S. C., Katzmann, D. J., Schnell, J. D., Sutanto, M., Emr, S. D. and Hicke, L. (2002). Epsins and Vps27p/Hrs contain ubiquitin-binding domains that function in receptor endocytosis. Nat. Cell Biol. 4, 389-393.
51. Sijen, T., Fleenor, J., Simmer, F., Thijssen, K. L., Parrish, S., Timmons, L., Plasterk, R. H. and Fire, A. (2001). On the role of RNA amplification in dsRNA-triggered gene silencing. Cell 107, 465-476.
52. Skeath, J. B. (1998). The Drosophila EGF receptor controls the formation and specification of neuroblasts along the dorsal-ventral axis of the Drosophila embryo. Development 125 3301-3312.
53. Sun, X. and Artavanis-Tsakonas, S. (1996). The intracellular deletions of Delta and Serrate define dominant negative forms of the Drosophila Notch ligands. Development 122, 2465-2474.
54. Sun, X. and Artavanis-Tsakonas, S. (1997). Secreted forms of DELTA and SERRATE define antagonists of Notch signaling in Drosophila. Development 124, 3439-3448.
55. Timmons, L. and Fire, A. (1998). Specific interference by ingested dsRNA. Nature 395, 854.
56. Wendland, B. (2002). Epsins: adaptors in endocytosis? Nat. Rev. Mol. Cell Biol. 3, 971-977.
57. Wendland, B., Steece, K. E. and Emr, S. D. (1999). Yeast epsin s contain an essential N-terminal ENTH domain, bind clathrin and are required for endocytosis. EMBO J. 18, 4383-4393.
58. Yeh, E., Dermer, M., Commisso, C., Zhou, L., McGlade, C. J. and Boulianne, G. L. (2001). Neuralized functions as an E3 ubiquitin ligase during Drosophila development. Curr. Biol. 11 1675-1679.
59. Yochem, J. and Greenwald, I. (1989). glp-1 and lin- 12, genes implicated in distinct cell-cell interactions in Caenorhabditis elegans, encode similar transmembrane proteins. Cell 58, 553-563.
60. Zetka, M. C., Kawasaki, I., Strome, S. and Muller, F. (1999). Synapsis and chiasma formation in Caenorhabditis elegans require HIM-3, a meiotic chromosome core component that functions in chromosome segregation. Genes Dev. 13, 2258-2270.
61. Zhang, F. L. and Casey, P. J. (1996). Protein prenylation: molecular mechanisms and functional consequences. Annu. Rev. Biochem. 65, 241-269.