Inheriting a structural scaffold for Golgi biosynthesis

BioEssays

Volumn 24, Issue 7, 2002, Pages 584-587

  Jesch, Stephen A ^a  

^a Department of Obstetrics Gynecology   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; BREFELDIN A; ENDOPLASMIC RETICULUM; GOLGI APPARATUS; MEMBRANE PROTEINS; MITOSIS; MODELS, BIOLOGICAL; PROTEIN SYNTHESIS INHIBITORS; ANIMALS; AUTOANTIGENS;

ANIMALIA;

AUTOANTIGEN; BREFELDIN A; GOLGIN SUBFAMILY A MEMBER 2; GORASP1 PROTEIN, HUMAN; MEMBRANE PROTEIN; PROTEIN SYNTHESIS INHIBITOR;

ANIMAL; ARTICLE; BIOLOGICAL MODEL; DRUG EFFECT; ENDOPLASMIC RETICULUM; GOLGI COMPLEX; METABOLISM; MITOSIS; PHYSIOLOGY;

EID: 0035996793     PISSN: 02659247     EISSN: None     Source Type: Journal    
DOI: 10.1002/bies.10122     Document Type: Article

References (28)

1. Partitioning of the matrix fraction of the Golgi apparatus during mitosis in animal cells
2. Mechanisms of intracellular protein transport
3. Inheriting the Golgi
4. Deconstructing Golgi inheritance
5. Golgi membranes are absorbed into and reemerge from the ER during mitosis
6. Golgi complex: Biogenesis de novo?
7. The concept of self-organization in cellular architecture
8. The Golgi and endoplasmic reticulum remain independent during mitosis in HeLa cells
9. Mitotic Golgi is in a dynamic equilibrium between clustered and free vesicles independent of the ER
10. Golgi clusters and vesicles mediate mitotic inheritance independently of the endoplasmic reticulum
11. Reorganization of the Golgi complex in association with mitosis: Redistribution of mannosidase II to the endoplasmic reticulum and effects of brefeldin A
12. Matrix proteins can generate the higher order architecture of the Golgi apparatus
13. Rapid redistribution of Golgi proteins into the ER in cells treated with brefeldin A: Evidence for membrane cycling from Golgi to ER
14. Maintenance of Golgi structure and function depends on the integrity of ER export
15. Evidence that the entire Golgi apparatus cycles in interphase HeLa cells: Sensitivity of Golgi matrix proteins to an ER exit block
16. Phosphorylation of the vesicle-tethering protein p115 by a casein kinase II-like enzyme is required for Golgi reassembly from isolated mitotic fragments
17. Stacking the cisternae
18. Cdc2 kinase directly phosphorylates the cis-Golgi matrix protein GM130 and is required for Golgi fragmentation in mitosis
19. MEK and Cdc2 kinase are sequentially required for Golgi disassembly in MDCK cells by the mitotic Xenopus extracts
20. Signaling via mitogen-activated protein kinase kinase (MEK1) is required for Golgi fragmentation during mitosis
21. Polo-like kinase is required for the fragmentation of pericentriolar Golgi stacks during mitosis
22. Mitotic phosphorylation of Golgi reassembly stacking protein 55 by mitogen-activated protein kinase ERK2
23. Peripheral Golgi protein GRASP65 is a target of mitotic polo-like kinase (PIk) and Cdc2
24. The vesicle docking protein p115 binds GM130, a cis-Golgi matrix protein, in a mitotically regulated manner
25. Structural elements common to mitosis and apoptosis
26. Caspase-2 is localized at the Golgi complex and cleaves golgin-160 during apoptosis
27. Caspase-mediated cleavage of the stacking protein GRASP65 is required for Golgi fragmentation during apoptosis
28. The effect of Golgi depletion on exocytic transport