Re'COG'nition at the Golgi

Traffic

Volumn 13, Issue 7, 2012, Pages 891-897

  Miller, Victoria J ^a   Ungar, Daniel ^a  

^a UNIVERSITY OF YORK   (United Kingdom)

Author keywords

CATCHR family; CDG; COG; Golgi; Membrane trafficking

Indexed keywords

CELL PROTEIN; CONSERVED OLIGOMERIC GOLGI 1; CONSERVED OLIGOMERIC GOLGI 2; CONSERVED OLIGOMERIC GOLGI 3; CONSERVED OLIGOMERIC GOLGI 4; CONSERVED OLIGOMERIC GOLGI 7; CONSERVED OLIGOMERIC GOLGI 8; UNCLASSIFIED DRUG;

ASPHYXIA; ATAXIA; BLOOD CLOTTING DISORDER; BRAIN ATROPHY; BRAIN HEMORRHAGE; FACE DYSMORPHIA; FAILURE TO THRIVE; FOCAL EPILEPSY; GENE DELETION; GLYCOSYLATION; GOLGI COMPLEX; GROWTH RETARDATION; HEART FAILURE; HEPATOSPLENOMEGALY; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INTRACELLULAR TRANSPORT; INTRON; JAUNDICE; KIDNEY FAILURE; LANGUAGE DISABILITY; LIVER CIRRHOSIS; MENTAL DEFICIENCY; MICROCEPHALY; MOLECULAR INTERACTION; MOTOR DYSFUNCTION; MUSCLE HYPOTONIA; POINT MUTATION; PRIORITY JOURNAL; PROTEIN DEFICIENCY; REINFECTION; REVIEW; SEIZURE; VITAMIN K DEFICIENCY; VOMITING;

ANIMALS; CONGENITAL DISORDERS OF GLYCOSYLATION; GLYCOSYLATION; GOLGI APPARATUS; HUMANS; PROTEIN PROCESSING, POST-TRANSLATIONAL; TRANSPORT VESICLES; VESICULAR TRANSPORT PROTEINS;

EID: 84862259443     PISSN: 13989219     EISSN: 16000854     Source Type: Journal    
DOI: 10.1111/j.1600-0854.2012.01338.x     Document Type: Review

References (55)

1. Krieger M, Brown MS, Goldstein JL. Isolation of Chinese hamster cell mutants defective in the receptor-mediated endocytosis of low density lipoprotein. J Mol Biol 1981;150:167-184.
2. Kingsley DM, Kozarsky KF, Segal M, Krieger M. Three types of low density lipoprotein receptor-deficient mutant have pleiotropic defects in the synthesis of N-linked, O-linked, and lipid-linked carbohydrate chains. J Cell Biol 1986;102:1576-1585.
3. Ungar D, Oka T, Brittle EE, Vasile E, Lupashin VV, Chatterton JE, Heuser JE, Krieger M, Waters MG. Characterization of a mammalian Golgi-localized protein complex, COG, that is required for normal Golgi morphology and function. J Cell Biol 2002;157:405-415.
4. Ungar D, Oka T, Krieger M, Hughson FM. Retrograde transport on the COG railway. Trends Cell Biol 2006;16:113-120.
5. Podos SD, Reddy P, Ashkenas J, Krieger M. LDLC encodes a brefeldin A-sensitive, peripheral Golgi protein required for normal Golgi function. J Cell Biol 1994;127:679-691.
6. Chatterton JE, Hirsch D, Schwartz JJ, Bickel PE, Rosenberg RD, Lodish HF, Krieger M. Expression cloning of LDLB, a gene essential for normal Golgi function and assembly of the ldlCp complex. Proc Natl Acad Sci U S A 1999;96:915-920.
7. Kim DW, Sacher M, Scarpa A, Quinn AM, Ferro-Novick S. High-copy suppressor analysis reveals a physical interaction between Sec34p and Sec35p, a protein implicated in vesicle docking. Mol Biol Cell 1999;10:3317-3329.
8. Spelbrink RG, Nothwehr SF. The yeast GRD20 gene is required for protein sorting in the trans-Golgi network/endosomal system and for polarization of the actin cytoskeleton. Mol Biol Cell 1999;10:4263-4281.
9. VanRheenen SM, Cao X, Lupashin VV, Barlowe C, Waters MG. Sec35p, a novel peripheral membrane protein, is required for ER to Golgi vesicle docking. J Cell Biol 1998;141:1107-1119.
10. VanRheenen SM, Cao X, Sapperstein SK, Chiang EC, Lupashin VV, Barlowe C, Waters MG. Sec34p and Sec35p are components of a protein complex required for vesicle tethering the yeast Golgi. J Cell Biol 1999;147:729-742.
11. Wuestehube LJ, Duden R, Eun A, Hamamoto S, Korn P, Ram R, Schekman R. New mutants of Saccharomyces cerevisiae affected in the transport of proteins from the endoplasmic reticulum to the Golgi complex. Genetics 1996;142:393-406.
12. Walter DM, Paul KS, Waters MG. Purification and characterization of a novel 13S hetero-oligomeric protein complex that stimulates in vitro Golgi transport. J Biol Chem 1998;273:29565-29576.
13. Suvorova ES, Kurten RC, Lupashin VV. Identification of a human orthologue of Sec34p as a component of the cis-Golgi vesicle tethering machinery. J Biol Chem 2001;276:22810-22818.
14. Loh E, Hong W. Sec34 is implicated in traffic from the endoplasmic reticulum to the Golgi and exists in a complex with GTC-90 and ldlBp. J Biol Chem 2002;277:21955-21961.
15. Ram RJ, Li B, Kaiser CA. Identification of Sec36p, Sec37p and Sec38p: components of the yeast complex that contains Sec34p and Sec35p. Mol Biol Cell 2002;13:1484-1500.
16. Suvorova ES, Duden R, Lupashin VV. 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 2002;157:631-643.
17. Whyte JRC, Munro S. 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 2001;1:527-537.
18. Oka T, Vasile E, Penman M, Novina CD, Dykxhoorn DM, Ungar D, Hughson FM, Krieger M. Genetic analysis of the subunit organization and function of the COG complex: studies of Cog5 and Cog7 deficient mammalian cells. J Biol Chem 2005;280:32736-32745.
19. Ungar D, Oka T, Vasile E, Krieger M, Hughson FM. Subunit map of the conserved oligomeric Golgi complex. J Biol Chem 2005;280:32729-32735.
20. Foulquier F, Ungar D, Reynders E, Zeevaert R, Mills P, Garcia-Silva MT, Briones P, Winchester B, Morelle W, Krieger M, Annaert W, Matthijs G. A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1-Cog8 interaction in COG complex formation. Hum Mol Genet 2007;16:717-730.
21. Fotso P, Koryakina Y, Pavliv O, Tsiomenko AB, Lupashin VV. Cog1p plays a central role in the organization of the yeast conserved oligomeric Golgi (COG) complex. J Biol Chem 2005:27613-27623.
22. Bruinsma P, Spelbrink RG, Nothwehr SF. Retrograde transport of the mannosyltransferase Och1p to the early Golgi requires a component of the COG transport complex. J Biol Chem 2004;279:39814-39823.
23. Oka T, Ungar D, Hughson FM, Krieger M. The COG and COPI complexes interact to control the abundance of GEARs, a subset of Golgi integral membrane proteins. Mol Biol Cell 2004;15:2423-2435.
24. Zolov SN, Lupashin VV. Cog3p depletion blocks vesicle-mediated Golgi retrograde trafficking in HeLa cells. J Cell Biol 2005;168:747-759.
25. Cavanaugh LF, Chen X, Richardson BC, Ungar D, Pelczer I, Rizo J, Hughson FM. Structural analysis of conserved oligomeric Golgi complex subunit 2. J Biol Chem 2007;282:23418-23426.
26. Richardson BC, Smith RD, Ungar D, Nakamura A, Jeffrey PD, Lupashin VV, Hughson FM. Structural basis for a human glycosylation disorder caused, in part, by mutation of the COG4 gene. Proc Natl Acad Sci U S A 2009;106:13329-13334.
27. Vasan N, Hutagalung A, Novick P, Reinisch KM. Structure of a C-terminal fragment of its Vps53 subunit suggests similarity of Golgi-associated retrograde protein (GARP) complex to a family of tethering complexes. Proc Natl Acad Sci U S A 2010;107:14176-14181.
28. Perez-Victoria FJ, Abascal-Palacios G, Tascon I, Kajava A, Magadan JG, Pioro EP, Bonifacino JS, Hierro A. Structural basis for the wobbler mouse neurodegenerative disorder caused by mutation in the Vps54 subunit of the GARP complex. Proc Natl Acad Sci U S A 2010;107:12860-12865.
29. Yu IM, Hughson FM. Tethering factors as organizers of intracellular vesicular traffic. Annu Rev Cell Dev Biol 2010;26:137-156.
30. Lees JA, Yip CK, Walz T, Hughson FM. Molecular organization of the COG vesicle tethering complex. Nat Struct Mol Biol 2010;17:1292-1297.
31. Shestakova A, Zolov S, Lupashin V. COG complex-mediated recycling of Golgi glycosyltransferases is essential for normal protein glycosylation. Traffic 2006;7:191-204.
32. Shestakova A, Suvorova E, Pavliv O, Khaidakova G, Lupashin V. Interaction of the conserved oligomeric Golgi complex with t-SNARE Syntaxin5a/Sed5 enhances intra-Golgi SNARE complex stability. J Cell Biol 2007;179:1179-1192.
33. Laufman O, Hong W, Lev S. The COG complex interacts directly with Syntaxin 6 and positively regulates endosome-to-TGN retrograde transport. J Cell Biol 2011;194:459-472.
34. Laufman O, Kedan A, Hong W, Lev S. Direct interaction between the COG complex and the SM protein, Sly1, is required for Golgi SNARE pairing. EMBO J 2009;28:2006-2017.
35. Ramirez IB, Lowe M. Golgins and GRASPs: holding the Golgi together. Semin Cell Dev Biol 2009;20:770-779.
36. Sohda M, Misumi Y, Yamamoto A, Nakamura N, Ogata S, Sakisaka S, Hirose S, Ikehara Y, Oda K. Interaction of Golgin-84 with the COG complex mediates the intra-Golgi retrograde transport. Traffic 2010;11:1552-1566.
37. Sohda M, Misumi Y, Yoshimura S, Nakamura N, Fusano T, Ogata S, Sakisaka S, Ikehara Y. The interaction of two tethering factors, p115 and COG complex, is required for Golgi integrity. Traffic 2007;8:270-284.
38. Vasile E, Oka T, Ericsson M, Nakamura N, Krieger M. IntraGolgi distribution of the conserved oligomeric Golgi (COG) complex. Exp Cell Res 2006;312:3132-3141.
39. Reynders E, Foulquier F, Leao Teles E, Quelhas D, Morelle W, Rabouille C, Annaert W, Matthijs G. Golgi function and dysfunction in the first COG4-deficient CDG type II patient. Hum Mol Genet 2009;18:3244-3256.
40. Wu X, Steet RA, Bohorov O, Bakker J, Newell J, Krieger M, Spaapen L, Kornfeld S, Freeze HH. Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder. Nat Med 2004;10:518-523.
41. Foulquier F, Vasile E, Schollen E, Callewaert N, Raemaekers T, Quelhas D, Jaeken J, Mills P, Winchester B, Krieger M, Annaert W, Matthijs G. Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II. Proc Natl Acad Sci U S A 2006;103:3764-3769.
42. Peanne R, Legrand D, Duvet S, Mir AM, Matthijs G, Rohrer J, Foulquier F. Differential effects of lobe A and lobe B of the conserved oligomeric Golgi complex on the stability of {beta}1, 4-galactosyltransferase 1 and {alpha}2, 6-sialyltransferase 1. Glycobiology 2011;21:864-876.
43. Pokrovskaya ID, Willett R, Smith RD, Morelle W, Kudlyk T, Lupashin VV. COG complex specifically regulates the maintenance of Golgi glycosylation machinery. Glycobiology 2011;21:1554-1569.
44. Spessott W, Uliana A, Maccioni HJ. Cog2 null mutant CHO cells show defective sphingomyelin synthesis. J Biol Chem 2010;285:41472-41482.
45. Oka T, Krieger M. Multi-component protein complexes and Golgi membrane trafficking. J Biochem 2005;137:109-114.
46. Luo L, Hannemann M, Koenig S, Hegermann J, Ailion M, Cho MK, Sasidharan N, Zweckstetter M, Rensing SA, Eimer S. The Caenorhabditis elegans GARP complex contains the conserved Vps51 subunit and is required to maintain lysosomal morphology. Mol Biol Cell 2011;22:2564-2578.
47. Jaeken J. Congenital disorders of glycosylation (CDG): it's (nearly) all in it!. J Inherit Metab Dis 2011;34:853-858.
48. Schnorrer F, Schonbauer C, Langer CC, Dietzl G, Novatchkova M, Schernhuber K, Fellner M, Azaryan A, Radolf M, Stark A, Keleman K, Dickson BJ. Systematic genetic analysis of muscle morphogenesis and function in Drosophila. Nature 2010;464:287-291.
49. Krieger M. Complementation of mutations in the LDL pathway of receptor-mediated endocytosis by cocultivation of LDL receptor-defective hamster cell mutants. Cell 1983;33:413-422.
50. Ng BG, Sharma V, Sun L, Loh E, Hong W, Tay SK, Freeze HH. Identification of the first COG-CDG patient of Indian origin. Mol Genet Metab 2011;102:364-367.
51. Zeevaert R, Foulquier F, Dimitrov B, Reynders E, Van Damme-Lombaerts R, Simeonov E, Annaert W, Matthijs G, Jaeken J. Cerebrocostomandibular-like syndrome and a mutation in the conserved oligomeric Golgi complex, subunit 1. Hum Mol Genet 2009;18:517-524.
52. Paesold-Burda P, Maag C, Troxler H, Foulquier F, Kleinert P, Schnabel S, Baumgartner M, Hennet T. Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation. Hum Mol Genet 2009;18:4350-4356.
53. Luebbehusen J, Thiel C, Rind N, Ungar D, Prinsen BHCMT, de Koning TJ, van Hasselt PM, Koerner C. Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation. Hum Mol Genet 2010;19:3623-3633.
54. Ng BG, Kranz C, Hagebeuk EE, Duran M, Abeling NG, Wuyts B, Ungar D, Lupashin V, Hartdorff CM, Poll-The BT, Freeze HH. Molecular and clinical characterization of a Moroccan Cog7 deficient patient. Mol Genet Metab 2007;91:201-204.
55. Kranz C, Ng BG, Sun L, Sharma V, Eklund EA, Miura Y, Ungar D, Lupashin V, Winkel RD, Cipollo JF, Costello CE, Loh E, Hong W, Freeze HH. COG8 deficiency causes new congenital disorder of glycosylation type IIh. Hum Mol Genet 2007;16:731-741.