Membrane fusion and the cell cycle: Cdc48p participates in the fusion of ER membranes

Cell

Volumn 82, Issue 6, 1995, Pages 885-893

  Latterich, Martin ^a   Fröhlich, Kai Uwe ^b   Schekman, Randy ^a  

^a University of California Berkeley   (United States)

^b UNIVERSITY OF TÜBINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; MEMBRANE PROTEIN; N ETHYLMALEIMIDE; POLYCLONAL ANTIBODY; PROTEIN ANTIBODY;

ANTIBODY SPECIFICITY; ARTICLE; CELL CYCLE; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; MEMBRANE FUSION; NONHUMAN; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEIN PURIFICATION; TEMPERATURE SENSITIVE MUTANT; YEAST;

EID: 0029122698     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/0092-8674(95)90268-6     Document Type: Article

References (35)

1. The formation of Golgi stacks from vesiculated Golgi membranes requires two distinct fusion events
2. Vesicular transport between the endoplasmic reticulum and the Golgi stack requires the NEM-sensitive fusion protein
3. Chromatography of proteins on hydroxyapatite
4. Purification of an N-ethylmaleimide-sensitive protein catalyzing vesicular transport
5. SNAPs, a family of NSF attachment proteins involved in intracellular membrane fusion in animals and yeast
6. Genetic control of the cell division cycle in yeast. III. Seven genes controlling nuclear division
7. Vesicle fusion following receptor-mediated endocytosis requires a protein active in Golgi transport
8. Characterization of a component of the yeast secretion machinery: identification of the SEC18 gene product
9. VCP, the mammalian homolog of cdc48, is tyrosine phosphorylated in response to T cell antigen receptor activation
10. PAS1, a yeast gene required for peroxisome biogenesis, encodes a member of a novel family of putative ATPases
11. Yeast cell cycle protein CDC48p shows fulllength homology to the mammalian protein VCP and is a member of a protein family involved in secretion, peroxisome formation, and gene expression
12. The ATPase activity of purified CDC48p from Saccharomyces cerevisiae shows complex dependency on ATP- ADP- and NADH-concentrations and is completely inhibited by NEM
13. The yeast SEC17 gene product is functionally equivalent to mammalian α-SNAP protein
14. Genetic control of the cell-division cycle in yeast. I. Detection of mutants
15. Different requirements for NSF, SNAP, and Rab proteins in apical and basolateral transport in MDCK cells
16. Use of a cDNA clone to identify a supposed precursor protein containing valosin
17. Nuclear congression and membrane fusion: two distinct events in the yeast karyogamy pathway
18. The karyogamy gene KAR2 and novel proteins are required for ER-membrane fusion
19. Role of an N-ethylmaleimide-sensitive transport component in promoting fusion of transport vesicles with cisternae of the Golgi stack
20. Coldsensitive cell-division-cycle mutants of yeast: isolation, properties, and pseudoreversion studies
21. An abundant and ubiquitous homo-oligomeric ring-shaped ATPase particle related to the putative vesicle fusion proteins Sec18p and NSF
22. Valosin-containing protein, VCP, is a ubiquitous clathrin-binding protein
23. Immunofluorescence methods for yeast
24. An NSF-like ATPase, p97, and NSF mediate cisternal regrowth from mitotic Golgi fragments
25. Distinct biochemical requirements for the budding, targeting, and fusion of ER-derived transport vesicles
26. Characteristics of endoplasmic reticulum-derived transport vesicles
27. Nuclear fusion in yeast
28. Implications of the SNARE hypothesis for intracellular membrane topology and dynamics
29. Tyrosine phosphorylation of VCP, the mammalian homologue of the Saccharomyces cerevisiae CDC48 protein, is unusually sensitive to stimulation by sodium vanadate and hydrogen peroxide
30. A Rab protein is required for the assembly of SNARE complexes in the docking of transport vesicles
31. AFG2, an essential gene in yeast, encodes anew member of the Sec18p, Past p, Cdc48p, TBP-1 family of putative ATPases
32. A fusion protein required for vesicle-mediated transport in both mammalian cells and yeast
33. Isolation and characterization of the principal ATPase associated with transitional endoplasmic reticulum of rat liver