Microscopic dissection of the process of stress granule assembly

Biochimica et Biophysica Acta - Molecular Cell Research

Volumn 1793, Issue 11, 2009, Pages 1728-1737

  Fujimura, Ken ^a,b   Katahira, Jun ^b   Kano, Fumi ^a   Yoneda, Yoshihiro ^b   Murata, Masayuki ^a  

^a UNIVERSITY OF TOKYO   (Japan)

^b OSAKA UNIVERSITY   (Japan)

Author keywords

Microtubule; Oxidative stress; RNA binding protein; Stress granule

Indexed keywords

DETERGENT; INITIATION FACTOR 2ALPHA; MESSENGER RNA; RNA BINDING PROTEIN;

ARTICLE; CELL COMPARTMENTALIZATION; CELL GRANULE; CELL STRESS; CELLULAR DISTRIBUTION; CONFOCAL MICROSCOPY; CONTROLLED STUDY; CYTOPLASM; DISSECTION; HELA CELL; HUMAN; HUMAN CELL; IMMUNOFLUORESCENCE; IN SITU HYBRIDIZATION; MICROSCOPY; MICROTUBULE; MOLECULAR INTERACTION; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEIN PHOSPHORYLATION;

CYTOPLASM; CYTOPLASMIC GRANULES; EUKARYOTIC INITIATION FACTOR-2; HELA CELLS; HUMANS; MICROSCOPY, CONFOCAL; PHOSPHORYLATION; RNA, MESSENGER; RNA-BINDING PROTEINS; STRESS, PHYSIOLOGICAL;

EID: 71749087672     PISSN: 01674889     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbamcr.2009.08.010     Document Type: Article

References (26)

1. Anderson P., and Kedersha N. Stress granules: the Tao of RNA triage. Trends Biochem. Sci. 33 (2008) 141-150
2. Kedersha N., Gupta M., Li W., Miller I., and Anderson P. RNA-binding proteins TIA-1 and TIAR link the phosphorylation of eIF2α to the assembly of mammalian stress granules. J. Cell Biol. 147 (1999) 1431-1442
3. Kedersha N., Stoecklin G., Ayodele M., Yacono P., Lykke-Andersen J., Fritzler M.J., Scheuner D., Kaufman R.J., Golan D.E., and Anderson P. Stress granules and processing bodies are dynamically linked sites of mRNP remodeling. J. Cell Biol. 169 (2005) 871-884
4. Kim W.J., Back S.H., Kim V., Ryu I., and Jang S.K. Sequestration of TRAF2 into stress granules interrupts tumor necrosis factor signaling under stress conditions. Mol. Cell. Biol. 25 (2005) 2450-2462
5. Hofmann I., Casella M., Schnolzer M., Schlechter T., Spring H., and Franke W.W. Identification of the junctional plaque protein plakophilin 3 in cytoplasmic particles containing RNA-binding proteins and the recruitment of plakophilins 1 and 3 to stress granules. Mol. Biol. Cell 17 (2006) 1388-1398
6. McEwen E., Kedersha N., Song B., Scheuner D., Gilks N., Han N., Chen J.-J., Anderson P., and Kaufman R.J. Heme-regulated inhibitor kinase-mediated phosphorylation of translation initiation factor 2 inhibits translation, induces stress granule formation and mediates survival upon arsenite exposure. J. Biol. Chem. 280 (2005) 16925-16933
7. Dang Y., Kedersha N., Low W.-K., Romo D., Gorospe M., Kaufman R., Anderson P., and Liu J.O. Eukaryotic initiation factor 2{alpha}-independent pathway of stress granule induction by the natural product pateamine A. J. Biol. Chem. 281 (2006) 32870-32878
8. Mazroui R., Sukarieh R., Bordeleau M.-E., Kaufman R.J., Northcote P., Tanaka J., Gallouzi I., and Pelletier J. Inhibition of ribosome recruitment induces stress granule formation independently of eukaryotic initiation factor 2{alpha} phosphorylation. Mol. Biol. Cell 17 (2006) 4212-4219
9. Gilks N., Kedersha N., Ayodele M., Shen L., Stoecklin G., Dember L.M., and Anderson P. Stress granule assembly is mediated by prion-like aggregation of TIA-1. Mol. Biol. Cell 15 (2004) 5383-5398
10. Tourriere H., Chebli K., Zekri L., Courselaud B., Blanchard J.M., Bertrand E., and Tazi J. The RasGAP-associated endoribonuclease G3BP assembles stress granules. J. Cell Biol. 160 (2003) 823-831
11. Wilczynska A., Aigueperse C., Kress M., Dautry F., and Weil D. The translational regulator CPEB1 provides a link between dcp1 bodies and stress granules. J. Cell Sci. 118 (2005) 981-992
12. Ohn T., Kedersha N., Hickman T., Tisdale S., and Anderson P. A functional RNAi screen links O-GlcNAc modification of ribosomal proteins to stress granule and processing body assembly. Nat. Cell Biol. 10 (2008) 1224-1231
13. Ivanov P.A., Chudinova E.M., and Nadezhdina E.S. Disruption of microtubules inhibits cytoplasmic ribonucleoprotein stress granule formation. Exp. Cell Res. 290 (2003) 227-233
14. Kwon S., Zhang Y., and Matthias P. The deacetylase HDAC6 is a novel critical component of stress granules involved in the stress response. Genes Dev. 21 (2007) 3381-3394
15. Kedersha N., Chen S., Gilks N., Li W., Miller I.J., Stahl J., and Anderson P. Evidence that ternary complex (eIF2-GTP-tRNAiMet)-deficient preinitiation complexes are core constituents of mammalian stress granules. Mol. Biol. Cell 13 (2002) 195-210
16. Kedersha N., Cho M.R., Li W., Yacono P.W., Chen S., Gilks N., Golan D.E., and Anderson D.E.P. Dynamic shuttling of TIA-1 accompanies the recruitment of mRNA to mammalian stress granules. J. Cell Biol. 151 (2000) 1257-1268
17. Mollet S., Cougot N., Wilczynska A., Dautry F., Kress M., Bertrand E., and Weil D. Translationally repressed mRNA transiently cycles through stress granules during stress. Mol. Biol. Cell 19 (2008) 4469-4479
18. Kolobova E., Efimov A., Kaverina I., Rishi A.K., Schrader J.W., Ham A.-J., Larocca M.C., and Goldenring J.R. Microtubule-dependent association of AKAP350A and CCAR-1 with RNA stress granules. Exp. Cell Res. 315 (2009) 542-555
19. Fujimura K., Kano F., and Murata M. Dual localization of the RNA binding protein CUGBP-1 to stress granule and perinucleolar compartment. Exp. Cell Res. 314 (2008) 543-553
20. Katahira J., Miki T., Takano K., Maruhashi M., Uchikawa M., Tachibana T., and Yoneda Y. Nuclear RNA export factor 7 is localized in processing bodies and neuronal granules through interactions with shuttling hnRNPs. Nucleic Acids Res. 36 (2008) 616-628
21. Tsai N.-P., Tsui N.-C., and Wei L.-N. Dynein motor contributes to stress granule dynamics in primary neurons. Neuroscience 159 (2009) 647-656
22. Burkhardt J.K., Echeverri C.J., Nilsson T., and Vallee R.B. Overexpression of the dynamitin (p50) subunit of the dynactin complex disrupts dynein-dependent maintenance of membrane organelle distribution. J. Cell Biol. 139 (1997) 469-484
23. Buchan J.R., Muhlrad D., and Parker R. P bodies promote stress granule assembly in Saccharomyces cerevisiae. J. Cell Biol. 183 (2008) 441-455
24. Kaiser T.E., Intine R.V., and Dundr M. De novo formation of a subnuclear body. Science 322 (2008) 1713-1717
25. Ben-Asouli Y., Banai Y., Pel-Or Y., Shir A., and Kaempfer R. Human interferon-γ mRNA autoregulates its translation through a pseudoknot that activates the interferon-inducible protein kinase PKR. Cell 108 (2002) 221-232
26. Kohrmann M., Luo M., Kaether C., DesGroseillers L., Dotti C.G., and Kiebler M.A. Microtubule-dependent recruitment of Staufen-green fluorescent protein into large RNA-containing granules and subsequent dendritic transport in living hippocampal neurons. Mol. Biol. Cell 10 (1999) 2945-2953