C. elegans as a model system to study the function of the COG complex in animal development

Biological Chemistry

Volumn 387, Issue 8, 2006, Pages 1031-1035

  Kubota, Yukihiko ^a   Nishiwaki, Kiyoji ^a  

^a RIKEN Center for Biosystems Dynamics Research   (Japan)

Author keywords

ADAM protease; Caenorhabditis elegans; COG complex; Glycosylation; Golgi enzyme; Organogenesis

Indexed keywords

COLLAGEN TYPE 14; DISINTEGRIN; METALLOPROTEINASE; TUMOR NECROSIS FACTOR ALPHA CONVERTING ENZYME;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; CAENORHABDITIS ELEGANS; CELLULAR DISTRIBUTION; CONSERVED OLIGOMERIC GOLGI COMPLEX; CONTROLLED STUDY; GOLGI COMPLEX; NONHUMAN; PRIORITY JOURNAL; PROTEIN GLYCOSYLATION; PROTEIN SECRETION; PROTEIN TARGETING; SHORT SURVEY;

ANIMALS; CAENORHABDITIS ELEGANS; GOLGI APPARATUS; MODELS, ANIMAL; MODELS, BIOLOGICAL; MULTIPROTEIN COMPLEXES;

ANIMALIA; CAENORHABDITIS ELEGANS;

EID: 33746930919     PISSN: 14316730     EISSN: 14374315     Source Type: Journal    
DOI: 10.1515/BC.2006.127     Document Type: Short Survey

References (43)

1. Aroian, R.V., Koga, M., Mendel, J.E., Ohshima, Y., and Sternberg, P.W. (1990). The let-23 gene necessary for Caenorhabditis elegans vulval induction encodes a tyrosine kinase of the EGF receptor subfamily. Nature 348, 693-699.
2. Baum, P.D. and Garriga, G. (1997). Neuronal migrations and axon fasciculation are disrupted in ina-1 integrin mutants. Neuron 19, 51-62.
3. Blelloch, R. and Kimble, J. (1999). Control of organ shape by a secreted metalloprotease in the nematode C. elegans. Nature 399, 586-590.
4. Brenner, S. (1974). The genetics of Caenorhabditis elegans. Genetics 77, 71-94.
5. Broadbent, I. D. and Pettitt, J. (2002). The C. elegans hmr-1 gene can encode a neuronal classic cadherin involved in the regulation of axon fasciculation. Curr. Biol. 12, 59-63.
6. Farkas, R.M., Giansanti, M.G., Gatti, M., and Fuller, M.T. (2003). The Drosophila Cog5 homologue is required for cytokinesis, cell elongation, and assembly of specialized Golgi architecture during spermatogenesis. Mol. Biol. Cell 14, 190-200.
7. Foulquier, F., Vasile, E., Schollen, E., Callewaert, N., Raemaekers, T., Quelhas, D., Jaeken, J., Mills, P., Winchester, B., Krieger, M., et al. (2006). Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II. Proc. Natl. Acad. Sci. USA 103, 3764-3769.
8. Greenwald, I. (1985). lin-12, a nematode homeotic gene, is homologous to a set of mammalian proteins that includes epidermal growth factor. Cell 43, 583-590.
9. Guo, X.D., Johnson, J.J., and Kramer, J.M. (1991). Embryonic lethality caused by mutations in basement membrane collagen of C. elegans. Nature 349, 707-709.
10. Hedgecock, E.M., Culotti, J.G., Hall, D.H., and Stern, B.D. (1987). Genetics of cell and axon migrations in Caenorhabditis elegans. Development 100, 365-382.
11. Hesselson, D., Newman, C., Kim, K.W., and Kimble, J. (2004). GON-1 and fibulin have antagonistic roles in control of organ shape. Curr. Biol. 14, 2005-2010.
12. Hill, R.J. and Sternberg, P.W. (1992). The gene lin-3 encodes an inductive signal for vulval development in C. elegans. Nature 358, 470-476.
13. Huang, X., Huang, P., Robinson, M.K., Stern, M.J., and Jin, Y. (2003). UNC-71, a disintegrin and metalloprotease (ADAM) protein, regulates motor axon guidance and sex myoblast migration. Development 130, 3147-3161.
14. Ishii, N., Wadsworth, W.G., Stern, B.D., Culotti, J.G., and Hedgecock, E.M. (1992). UNC-6, a laminin-related protein, guides cell and pioneer axon migrations in C. elegans. Neuron 9, 873-881.
15. Kimble, J. and Hirsh, D. (1979). The postembryonic cell lineages of the hermaphrodite and male gonads in Caenorhabditis elegans. Dev. Biol. 70, 396-417.
16. Kimble, J.E. and White, J.G. (1981). On the control of germ cell development in Caenorhabditis elegans. Dev. Biol. 81, 208-219.
17. Kingsley, D.M., Kozarsky, K.F., Segal, M., and Krieger, M. (1986). Three types of low density lipoprotein receptor-deficient mutant have pleiotropic defects in the synthesis of N-liked, O-linked, and lipid-linked carbohydrate chains. J. Cell Biol. 102, 1576-1685.
18. Krieger, M.M., Brown, S., and Goldstein, J.L. (1981). Isolation of Chinese hamster cell mutants with defects in the receptor-mediated endocytosis of low density lipoprotein. J. Mol. Biol. 150, 167-184.
19. Kubota, Y., Kuroki, R., and Nishiwaki, K. (2004). A fibulin-1 homolog interacts with an ADAM protease that controls cell migration in C. elegans. Curr. Biol. 14, 2011-2018.
20. Kubota, Y., Sano, M., Goda, S., Suzuki, N., and Nishiwaki, K. (2006). The conserved oligomeric Golgi complex acts in organ morphogenesis via glycosylation of an ADAM protease in C. elegans. Development 133, 263-273.
21. Loh, E. and Hong, W. (2004). The binary interacting network of the conserved oligomeric Golgi tethering complex. J. Biol. Chem. 279, 24640-24648.
22. Marquardt, T. and Denecke, J. (2003). Congenital disorders of glycosylation: review of their molecular bases, clinical presentations and specific therapies. Eur. J. Pediatr. 162, 359-379.
23. Nishiwaki, K., Hisamoto, N., and Matsumoto, K. (2000). A metalloprotease disintegrin that controls cell migration in Caenorhabditis elegans. Science 288, 2205-2208.
24. Nishiwaki, K., Kubota, Y., Chigira, Y., Roy, S.M., Suzuki, M., Schvarzstein, M., Jigami, Y., Hisamoto, N., and Matsumoto, K. (2004). An NDPase links ADAM protease glycosylation with organ morphogenesis in C. elegans. Nat. Cell Biol. 6, 31-37.
25. Oka, T. and Krieger, M. (2005). Multi-component protein complexes and Golgi membrane trafficking. J. Biochem. 137, 109-114.
26. Oka, T., Ungar, D., Hughson, F.M., and Krieger, M. (2004). The COG and COPI complexes interact to control the abundance of GEARs, a subset of Golgi integral membrane proteins. Mol. Biol. Cell 15, 2423-2435.
27. Podos, S.D., Reedy, P., Ashkenas, J., and Krieger, M. (1994). LDLC encodes a brefeldin A-sensitive, peripheral Golgi protein required for normal Golgi function. J. Cell Biol. 127, 679-691.
28. Reddy, P. and Krieger, M. (1989). Isolation and characterization of an extragenic suppressor of the low-density lipoprotein receptor-deficient phenotype of a Chinese hamster ovary cell mutant. Mol. Cell. Biol. 9, 4799-4806.
29. Rogalski, T.M., Williams, B.D., Mullen, G.P., and Moerman, D.G. (1993). Products of the unc-52 gene in Caenorhabditis elegans are homologous to the core protein of the mammalian basement membrane heparan sulfate proteoglycan. Genes Dev. 7, 1471-1484.
30. Shioi, G., Shoji, M., Nakamura, M., Ishihara, T., Katsura, I., Fujisawa, H., and Takagi, S. (2001). Mutations affecting nerve attachment of Caenorhabditis elegans. Genetics 157, 1611-1622.
31. Sibley, M.H., Johnson, J.J., Mello, C.C., and Kramer, J.M. (1993). Genetic identification, sequence, and alternative splicing of the Caenorhabditis elegans α2(IV) collagen gene. J. Cell Biol. 123, 255-264.
32. Spelbrink, R.G. and Nothwehr, S.F. (1999). The yeast GRD20 gene is required for protein sorting in the trans-Golgi network/endosomal system and polarization of the actin cytoskeleton. Mol. Biol. Cell 10, 4263-4281.
33. Spike, C.A., Davies, A.G., Shaw, J.E., and Herman, R.K. (2002). MEC-8 regulates alternative splicing of unc-52 transcripts in C. elegans hypodermal cells. Development 129, 4999-5008.
34. Sulston, J.E. and Horvitz, H.R. (1977). Post-embryonic cell lineages of the nematode, Caenorhabditis elegans. Dev. Biol. 56, 110-156.
35. Sulston, J.E., Schierenberg, E., White, J.G., and Thomson, J.N. (1983). The embryonic cell lineage of the nematode Caenorhabditis elegans. Dev. Biol. 100, 64-119.
36. Suvorova, E.S., Duden, R., and Lupashin, V.V. (2002). The Sec34/ Sec35p complex, a Ypt1p effector required for retrograde intra-Golgi trafficking, interacts with Golgi SNAREs and COPI vesicle coat proteins. J. Cell Biol. 157, 631-643.
37. Ungar, D., Oka, T., Brittle, E.E., Vasile, E., Lupashin, V.V., Chatterton, J.E., Heuser, J.E., Krieger, M., and Waters, M.G. (2002). Characterization of a mammalian Golgi-localized protein complex, COG, that is required for normal Golgi morphology and function. J. Cell Biol. 157, 405-414.
38. Ungar, D., Oka, T., Krieger, M., and Hughson, F.M. (2006). Retrograde transport on the COG railway. Trends Cell Biol. 16, 113-120.
39. Wadsworth, W.G., Bhatt, H., and Hedgecock, E.M. (1996). Neuroglia and pioneer neurons express UNC-6 to provide global and local netrin cues for guiding migrations in C. elegans. Neuron 16, 35-46.
40. Walter, D.M., Paul, K.S., and Waters, M.G. (1998). Purification and characterization of novel 13S hetero-oligomeric protein complex that stimulates in vitro Golgi transport. J. Biol. Chem. 273, 29565-29576.
41. Whyte, J.R.C. and Munro, S. (2001). The Sec34/35 Golgi transport complex is related to the exocyst, defining a family of complexes involved in multiple steps of membrane traffic. Dev. Cell 1, 527-537.
42. Wu, X., Steet, R.A., Bohorov, O., Bakker, J., Newell, J., Krieger, M., Spaapen, L., Kornfeld, S., and Freeze, H.H. (2004). Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder. Nat. Med. 10, 518-523.
43. Wuestehube, L.J., Duden, R., Eun, A., Hamamoto, S., Korn, P., Ram, R., and Schekman, R. (1996). New mutants of Saccharomyces cerevisiae affected in the transport of proteins from endoplasmic reticulum to the Golgi complex. Genetics 142, 393-406.