Disruption of microtubules inhibits cytoplasmic ribonucleoprotein stress granule formation

Experimental Cell Research

Volumn 290, Issue 2, 2003, Pages 227-233

  Ivanov, Pavel A ^a,b   Chudinova, Elena M ^a   Nadezhdina, Elena S ^a,b  

^a INSTITUTE OF PROTEIN RESEARCH   (Russian Federation)

^b MOSCOW STATE UNIVERSITY   (Russian Federation)

Author keywords

Actin; Arsenate; eIF3a; Latrunculin B; Microtubule; Nocodazole; PABP; Paclitaxel; Stress granules; Translation initiation factor 3

Indexed keywords

ARSENATE SODIUM; BINDING PROTEIN; INITIATION FACTOR 3; LATRUNCULIN B; NOCODAZOLE; PACLITAXEL; POLYADENYLIC ACID; PROTEIN ANTIBODY; PROTEIN DERIVATIVE; PROTEIN P170; RIBONUCLEOPROTEIN; UNCLASSIFIED DRUG; VINBLASTINE;

ACTIN FILAMENT; ANIMAL CELL; ANIMAL CELL CULTURE; ANTIBODY LABELING; ARTICLE; CONTROLLED STUDY; CYTOPLASM; CYTOSKELETON; DEPOLYMERIZATION; GRANULE CELL; IMMUNOFLUORESCENCE; MICROTUBULE; MICROTUBULE ASSEMBLY; NONHUMAN; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; STRESS;

EID: 0142026265     PISSN: 00144827     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-4827(03)00290-8     Document Type: Article

References (27)

1. Nover L., Scharf K.D., Neumann D. Formation of cytoplasmic heat shock granules in tomato cell cultures and leaves. Mol. Cell. Biol. 3:1983;1648-1655.
2. Nover L., Scharf K.D., Neumann D. Cytoplasmic heat shock granules are formed from precursor particles and are associated with a specific set of mRNAs. Mol. Cell. Biol. 9:1989;1298-1308.
3. Scharf K.D., Heider H., Hohfeld I., Lyck R., Schmidt E., Nover L. The tomato Hsf system HsfA2 needs interaction with HsfA1 for efficient nuclear import and may be localized in cytoplasmic heat stress granules . Mol. Cell. Biol. 18:1998;2240-2251.
4. Kedersha N.L., Gupta M., Li W., Miller I., Anderson P. RNA-binding proteins TIA-1 and TIAR link the phosphorylation of eIF-2 alpha to the assembly of mammalian stress granules. J. Cell Biol. 147:1999;1431-1442.
5. Kedersha N., Cho M.R., Li W., Yacono P.W., Chen S., Gilks N., Golan D.E., Anderson P. Dynamic shuttling of TIA-1 accompanies the recruitment of mRNA to mammalian stress granules. J. Cell Biol. 151:2000;1257-1268.
6. Kedersha N., Chen S., Gilks N., Li W., Miller I.J., Stahl J., Anderson P. Evidence that ternary complex (eIF2-GTP-tRNA(i)(Met))-deficient preinitiation complexes are core constituents of mammalian stress granules. Mol. Biol. Cell. 13:2002;195-210.
7. Luby-Phelps K. Cytoarchitecture and physical properties of cytoplasm volume, viscosity, diffusion, intracellular surface area . Int. Rev. Cytol. 192:2000;189-221.
8. Bomsel M., Parton R., Kuznetsov S.A., Schroer T.A., Gruenberg J. Microtubule- and motor-dependent fusion in vitro between apical and basolateral endocytic vesicles from MDCK cells. Cell. 62:1990;719-731.
9. Bassell G.J., Singer R.H., Kosik K.S. Association of poly(A) mRNA with microtubules in cultured neurons. Neuron. 12:1994;571-582.
10. Pokrywka N.J., Stephenson E.C. Microtubules are a general component of mRNA localization systems in Drosophila oocytes. Dev. Biol. 167:1995;363-370.
11. Arn E.A., MacDonald P.M. Motors driving mRNA localization new insights from in vivo imaging . Cell. 95:1998;151-154.
12. Carson J.H., Worboys K., Ainger K., Barbarese E. Translocation of myelin basic protein mRNA in oligodendrocytes requires microtubules and kinesin. Cell Motil. Cytol. 38:1997;318-328.
13. Sundell C.L., Singer R.H. Requirement of microfilaments in sorting of actin messenger RNA. Science. 253:1991;1275-1277.
14. Shanina N.A., Ivanov P.A., Chudinova E.M., Severin F.F., Nadezhdina E.S. Translation initiation factor eIF3 is able to bind with microtubules in mammalian cells. Mol. Biol. (Mosk.). 35:2001;638-646.
15. Moore R.C., Cyr R.J. Association between elongation factor-1 alpha and microtubules in vivo is domain dependent and conditional. Cell Motil. Cytoskel. 45:2000;279-292.
16. Liu G., Grant W.M., Persky D., Latham V.M. Jr., Singer R.H., Condeelis J. Interactions of elongation factor 1 alpha with F-actin and beta-actin mRNA implications for anchoring mRNA in cell protrusions . Mol. Biol. Cell. 13:2002;579-592.
17. Liu G., Tang J., Edmonds B.T., Murray J., Levin S., Condeelis J. F-actin sequesters elongation factor 1 alpha from interaction with aminoacyl-tRNA in a pH-dependent reaction. J. Cell Biol. 135:1996;953-963.
18. Ruzanov P.V., Evdokimova V.M., Korneeva N.L., Hershey J.W., Ovchinnikov L.P. Interaction of the universal mRNA-binding protein, p50, with actin a possible link between mRNA and microfilaments . J. Cell Sci. 112:1999;3487-3496.
19. Bektas M., Nurten R., Sayers Z., Bermek E. Interactions of elongation factor 2 with the cytoskeleton and interference with DNase I binding to actin. Eur. J. Biochem. 256:1998;142-147.
20. Shestakova E.A., Motuz L.P., Minin A.A., Gelfand V.I., Gavrilova L.P. Some of eukaryotic elongation factor 2 is colocalized with actin microfilament bundles in mouse embryo fibroblasts. Cell Biol. Int. Rep. 15:1991;75-84.
21. Rosette C., Karin M. Cytoskeletal control of gene expression depolymerization of microtubules activates NF-kappa B. J. Cell Biol. 128:1995;1111-1119.
22. Ivanova T.V., Ivanov V.N., Nadezhdina E.S. Transcription factors NF-kappaB and AP-1/c-fos in cell response to nocodazole. Membr. Cell Biol. 14:2001;727-741.
23. Blagosklonny M.V., Fojo T. Molecular effects of paclitaxel myths and reality (a critical review) . Int. J. Cancer. 83:1999;151-156.
24. Al-Haddad A., Shonn M.A., Redlich B., Blocker A., Burkhardt J.K., Yu H., Hammer J.A. 3rd, Weiss D.G., Steffen W., Griffiths G., Kuznetsov S.A. Myosin Va bound to phagosomes binds to F-actin and delays microtubule-dependent motility. Mol. Biol. Cell. 12:2001;2742-2755.
25. J.K. Yisraeli, S. Sokol, D.A. Melton, A two-step model for the localization of maternal mRNA in Xenopus oocytes: involvement of microtubules and microfilaments in the translocation and anchoring of Vg1 mRNA, Development 108 (1990).
26. Brendza R.P., Serbus L.R., Duffy J.B., Saxton W.M. A function for kinesin I in the posterior transport of oskar mRNA and Staufen protein. Science. 289:2000;2120-2122.
27. Knowles R.B., Sabry J.H., Martone M.E., Deerinck T.J., Ellisman M.H., Bassell G.J., Kosik K.S. Translocation of RNA granules in living neurons. J. Neurosci. 16:1996;7812-7820.