Role of dynein in viral pathogenesis

Dyneins

Volumn , Issue , 2012, Pages 560-583

  Mouland, Andrew J ^a,b   Milev, Miroslav P ^a,b  

^a MCGILL UNIVERSITY   (Canada)

^b MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84882304463     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B978-0-12-382004-4.10022-6     Document Type: Chapter

References (133)

1. Girard M.P., Bansal G.P. HIV/AIDS vaccines: A need for new concepts?. Int. Rev. Immunol. 2008, 27:447-471.
2. Rerks-Ngarm S., Pitisuttithum P., Nitayaphan S., Kaewkungwal J., Chiu J., Paris R., Premsri N., Namwat C., de Souza M., Adams E., Benenson M., Gurunathan S., Tartaglia J., McNeil J.G., Francis D.P., Stablein D., Birx D.L., Chunsuttiwat S., Khamboonruang C., Thongcharoen P., Robb M.L., Michael N.L., Kunasol P., Kim J.H. Vaccination with ALVAC and AIDSVAX to prevent HIV-1 infection in Thailand. New Eng. J. Med. 2009, 361:2209-2220.
3. Zhou T., Georgiev I., Wu X., Yang Z.Y., Dai K., Finzi A., Do Kwon Y., Scheid J., Shi W., Xu L., Yang Y., Zhu J., Nussenzweig M.C., Sodroski J., Shapiro L., Nabel G.J., Mascola J.R., Kwong P.D. Structural basis for broad and potent neutralization of HIV-1 by antibody VRC01. Science 2010, 329:1060-1064.
4. Fontenot D.R., den Hollander P., Vela E.M., Newman R., Sastry J.K., Kumar R. Dynein light chain 1 peptide inhibits human immunodeficiency virus infection in eukaryotic cells. Biochem. Biophys. Res. Commun. 2007, 363:901-907.
5. Cullen B.R. Nuclear mRNA export: Insights from virology. Trends Biochem. Sci. 2003, 28:419-424.
6. Hauber I., Bevec D., Heukeshoven J., Kratzer F., Horn F., Choidas A., Harrer T., Hauber J. Identification of cellular deoxyhypusine synthase as a novel target for antiretroviral therapy. J. Clin. Invest. 2005, 115:76-85.
7. Dejesus E., Berger D., Markowitz M., Cohen C., Hawkins T., Ruane P., Elion R., Farthing C., Zhong L., Cheng A.K., McColl D., Kearney B.P. Antiviral activity, pharmacokinetics, and dose response of the HIV-1 integrase inhibitor GS-9137 (JTK-303) in treatment-naive and treatment-experienced patients. J. Acquir. Immune Defic. Syndr. 2006, 43:1-5.
8. Piller S.C., Caly L., Jans D.A. Nuclear import of the pre-integration complex (PIC): The Achilles heel of HIV?. Curr. Drug Targets 2003, 4:409-429.
9. Zhou J., Yuan X., Dismuke D., Forshey B.M., Lundquist C., Lee K.H., Aiken C., Chen C.H. Small-molecule inhibition of human immunodeficiency virus type 1 replication by specific targeting of the final step of virion maturation. J. Virol. 2004, 78:922-929.
10. Li F., Goila-Gaur R., Salzwedel K., Kilgore N.R., Reddick M., Matallana C., Castillo A., Zoumplis D., Martin D.E., Orenstein J.M., Allaway G.P., Freed E.O., Wild C.T. PA-457: A potent HIV inhibitor that disrupts core condensation by targeting a late step in Gag processing. Proc. Natl. Acad. Sci. USA 2003, 100. 13 555-13 560.
11. Bar-Magen T., Sloan R.D., Donahue D.A., Kuhl B.D., Zabeida A., Xu H., Oliveira M., Hazuda D.J., Wainberg M.A. Identification of novel mutations responsible for resistance to MK-2048, a second-generation HIV-1 integrase inhibitor. J. Virol. 2010, 84:9210-9216.
12. Adamson C.S., Salzwedel K., Freed E.O. Virus maturation as a new HIV-1 therapeutic target. Expert Opin. Ther. Tar. 2009, 13:895-908.
13. Waheed A.A., Freed E.O. Peptide inhibitors of HIV-1 egress. ACS Chem. Biol. 2008, 3:745-747.
14. Bushman F.D., Malani N., Fernandes J., D'Orso I., Cagney G., Diamond T.L., Zhou H., Hazuda D.J., Espeseth A.S., Konig R., Bandyopadhyay S., Ideker T., Goff S.P., Krogan N.J., Frankel A.D., Young J.A., Chanda S.K. Host cell factors in HIV replication: Meta-analysis of genome-wide studies. PLoS Pathog 2009, 5:e1000437.
15. Adamson C.S., Freed E.O. Novel approaches to inhibiting HIV-1 replication. Antivir. Res. 2010, 85:119-141.
16. An P., Winkler C.A. Host genes associated with HIV/AIDS: Advances in gene discovery. Trends Genet. 2010, 26:119-131.
17. Arhel N., Kirchhoff F. Host proteins involved in HIV infection: New therapeutic targets. Biochim. Biophys. Acta 2010, 1802:313-321.
18. Cantin R., Methot S., Tremblay M.J. Plunder and stowaways: Incorporation of cellular proteins by enveloped viruses. J. Virol. 2005, 79:6577-6587.
19. Sowinski S., Jolly C., Berninghausen O., Purbhoo M.A., Chauveau A., Kohler K., Oddos S., Eissmann P., Brodsky F.M., Hopkins C., Onfelt B., Sattentau Q., Davis D.M. Membrane nanotubes physically connect T cells over long distances presenting a novel route for HIV-1 transmission. Nat. Cell. Biol. 2008, 10:211-219.
20. Lehmann M.J., Sherer N.M., Marks C.B., Pypaert M., Mothes W. Actin- and myosin-driven movement of viruses along filopodia precedes their entry into cells. J. Cell Biol. 2005, 170:317-325.
21. Sherer N.M., Lehmann M.J., Jimenez-Soto L.F., Horensavitz C., Pypaert M., Mothes W. Retroviruses can establish filopodial bridges for efficient cell-to-cell transmission. Nat. Cell. Biol. 2007, 9:310-315.
22. Luby-Phelps K. Cytoarchitecture and physical properties of cytoplasm: Volume, viscosity, diffusion, intracellular surface area. Int. Rev. Cytol 2000, 192:189-221.
23. Bremner K.H., Scherer J., Yi J., Vershinin M., Gross S.P., Vallee R.B. Adenovirus transport via direct interaction of cytoplasmic dynein with the viral capsid hexon subunit. Cell Host Microbe. 2009, 6:523-535.
24. Kelkar S.A., Pfister K.K., Crystal R.G., Leopold P.L. Cytoplasmic dynein mediates adenovirus binding to microtubules. J. Virol. 2004, 78. 10122-10132.
25. Suomalainen M., Nakano M.Y., Boucke K., Keller S., Greber U.F. Adenovirus-activated PKA and p38/MAPK pathways boost microtubule-mediated nuclear targeting of virus. EMBO J. 2001, 20:1310-1319.
26. Lukashok S.A., Tarassishin L., Li Y., Horwitz M.S. An adenovirus inhibitor of tumor necrosis factor alpha-induced apoptosis complexes with dynein and a small GTPase. J. Virol. 2000, 74:4705-4709.
27. Alonso C., Miskin J., Hernaez B., Fernandez-Zapatero P., Soto L., Canto C., Rodriguez-Crespo I., Dixon L., Escribano J.M. African swine fever virus protein p54 interacts with the microtubular motor complex through direct binding to light-chain dynein. J. Virol. 2001, 75:9819-9827.
28. Hernaez B., Diaz-Gil G., Garcia-Gallo M., Ignacio Quetglas J., Rodriguez-Crespo I., Dixon L., Escribano J.M., Alonso C. The African swine fever virus dynein-binding protein p54 induces infected cell apoptosis. FEBS Lett. 2004, 569:224-228.
29. Kubota T., Matsuoka M., Chang T.H., Bray M., Jones S., Tashiro M., Kato A., Ozato K. Ebolavirus VP35 interacts with the cytoplasmic dynein light chain 8. J. Virol. 2009, 83:6952-6956.
30. Ramanathan H.N., Chung D.H., Plane S.J., Sztul E., Chu Y.K., Guttieri M.C., McDowell M., Ali G., Jonsson C.B. Dynein-dependent transport of the hantaan virus nucleocapsid protein to the endoplasmic reticulum-Golgi intermediate compartment. J. Virol. 2007, 81:8634-8647.
31. Douglas M.W., Diefenbach R.J., Homa F.L., Miranda-Saksena M., Rixon F.J., Vittone V., Byth K., Cunningham A.L. Herpes simplex virus type 1 capsid protein VP26 interacts with dynein light chains RP3 and Tctex1 and plays a role in retrograde cellular transport. J. Biol. Chem. 2004, 279. 28522-28530.
32. Dohner K., Radtke K., Schmidt S., Sodeik B. Eclipse phase of herpes simplex virus type 1 infection: Efficient dynein-mediated capsid transport without the small capsid protein VP26. J. Virol. 2006, 80:8211-8224.
33. Frampton A.R., Uchida H., von Einem J., Goins W.F., Grandi P., Cohen J.B., Osterrieder N., Glorioso J.C. Equine herpesvirus type 1 (EHV-1) utilizes microtubules, dynein, and ROCK1 to productively infect cells. Vet. Microbiol. 2010, 141:12-21.
34. Radtke K., Kieneke D., Wolfstein A., Michael K., Steffen W., Scholz T., Karger A., Sodeik B. Plus- and minus-end directed microtubule motors bind simultaneously to herpes simplex virus capsids using different inner tegument structures. PLoS Pathog. 2010, 6:e1000991.
35. Mueller S., Cao X., Welker R., Wimmer E. Interaction of the poliovirus receptor CD155 with the dynein light chain Tctex-1 and its implication for poliovirus pathogenesis. J. Biol. Chem. 2002, 277:7897-7904.
36. Ohka S., Sakai M., Bohnert S., Igarashi H., Deinhardt K., Schiavo G., Nomoto A. Receptor-dependent and -independent axonal retrograde transport of poliovirus in motor neurons. J. Virol. 2009, 83:4995-5004.
37. Yamada M., Toba S., Yoshida Y., Haratani K., Mori D., Yano Y., Mimori-Kiyosue Y., Nakamura T., Itoh K., Fushiki S., Setou M., Wynshaw-Boris A., Torisawa T., Toyoshima Y.Y., Hirotsune S. LIS1 and NDEL1 coordinate the plus-end-directed transport of cytoplasmic dynein. EMBO J. 2008, 27:2471-2483.
38. Kondratova A.A., Neznanov N., Kondratov R.V., Gudkov A.V. Poliovirus protein 3A binds and inactivates LIS1, causing block of membrane protein trafficking and deregulation of cell division. Cell Cycle (Georgetown, Tex.) 2005, 4:1403-1410.
39. Ma S., Chisholm R.L. Cytoplasmic dynein-associated structures move bidirectionally in vivo. J. Cell Sci. 2002, 115:1453-1460.
40. Florin L., Becker K.A., Lambert C., Nowak T., Sapp C., Strand D., Streeck R.E., Sapp M. Identification of a dynein interacting domain in the papillomavirus minor capsid protein l2. J. Virol. 2006, 80:6691-6696.
41. Schneider M.A., Spoden G.A., Florin L., Lambert C. Identification of the dynein light chains required for human papillomavirus infection. Cellular Microbiology 2010, 13:32-46.
42. Jacob Y., Badrane H., Ceccaldi P.E., Tordo N. Cytoplasmic dynein LC8 interacts with lyssavirus phosphoprotein. J. Virol. 2000, 74:10217-10222.
43. Mebatsion T. Extensive attenuation of rabies virus by simultaneously modifying the dynein light chain binding site in the P protein and replacing Arg333 in the G protein. J. Virol. 2001, 75. 11496-11502.
44. Rasalingam P., Rossiter J.P., Mebatsion T., Jackson A.C. Comparative pathogenesis of the SAD-L16 strain of rabies virus and a mutant modifying the dynein light chain binding site of the rabies virus phosphoprotein in young mice. Virus Res. 2005, 111:55-60.
45. Raux H., Flamand A., Blondel D. Interaction of the rabies virus P protein with the LC8 dynein light chain. J. Virol. 2000, 74:10212-10216.
46. Poisson N., Real E., Gaudin Y., Vaney M.C., King S., Jacob Y., Tordo N., Blondel D. Molecular basis for the interaction between rabies virus phosphoprotein P and the dynein light chain LC8: Dissociation of dynein-binding properties and transcriptional functionality of P. J. Gen. Virol. 2001, 82:2691-2696.
47. Tan G.S., Preuss M.A., Williams J.C., Schnell M.J. The dynein light chain 8 binding motif of rabies virus phosphoprotein promotes efficient viral transcription. Proc. Natl. Acad. Sci. USA 2007, 104:7229-7234.
48. Naranatt P.P., Krishnan H.H., Smith M.S., Chandran B. Kaposi's sarcoma-associated herpesvirus modulates microtubule dynamics via RhoA-GTP-diaphanous 2 signaling and utilizes the dynein motors to deliver its DNA to the nucleus. J. Virol. 2005, 79:1191-1206.
49. McDonald D., Vodicka M., Lucero G., Svitkina Y., Borisy G., Emerman M., Hope T.J. Visualization of the intracellular behavior of HIV in living cells. J. Cell Biol. 2002, 159:441-452.
50. Petit C., Giron M.L., Tobaly-Tapiero J., Bittoun P., Real E., Jacob Y., Tordo N., De The H., Saib A. Targeting of incoming retroviral Gag to the centrosome involves a direct interaction with the dynein light chain 8. J. Cell Sci. 2003, 116:3433-3442.
51. Su Y., Qiao W., Guo T., Tan J., Li Z., Chen Y., Li X., Li Y., Zhou J., Chen Q. Microtubule-dependent retrograde transport of bovine immunodeficiency virus. Cell. Microbiol. 2010, 12:1098-1107.
52. Carty M., Bowie A.G. Recent insights into the role of toll-like receptors in viral infection. Clin. Exp. Immunol. 2010, 161:397-406.
53. Thompson A.J., Locarnini S.A. Toll-like receptors, RIG-I-like RNA helicases and the antiviral innate immune response. Immunol. Cell Biol. 2007, 85:435-445.
54. Taylor D.R., Lee S.B., Romano P.R., Marshak D.R., Hinnebusch A.G., Esteban M., Mathews M.B. Autophosphorylation sites participate in the activation of the double-stranded-RNA-activated protein kinase PKR. Mol. Cell. Biol. 1996, 16:6295-6302.
55. Bonjardim C.A., Ferreira P.C., Kroon E.G. Interferons: Signaling, antiviral and viral evasion. Immunol. Lett. 2009, 122:1-11.
56. Douglas J.L., Gustin J.K., Viswanathan K., Mansouri M., Moses A.V., Fruh K. The great escape: Viral strategies to counter BST-2/tetherin. PLoS Pathog. 2010, 6:e1000913.
57. Carthagena L., Bergamaschi A., Luna J.M., David A., Uchil P.D., Margottin-Goguet F., Mothes W., Hazan U., Transy C., Pancino G., Nisole S. Human TRIM gene expression in response to interferons. PLoS One 2009, 4:e4894.
58. Douville R.N., Hiscott J. The interface between the innate interferon response and expression of host retroviral restriction factors. Cytokine 2010, 52:108-115.
59. Schutz S., Sarnow P. How viruses avoid stress. Cell Host Microbe. 2007, 2:284-285.
60. Mogensen T.H., Melchjorsen J., Larsen C.S., Paludan S.R. Innate immune recognition and activation during HIV infection. Retrovirology 2010, 7:54.
61. Martinelli E., Cicala C., Van Ryk D., Goode D.J., Macleod K., Arthos J., Fauci A.S. HIV-1 gp120 inhibits TLR9-mediated activation and IFN-α secretion in plasmacytoid dendritic cells. Proc. Natl. Acad. Sci. USA 2007, 104:3396-3401.
62. Doehle B.P., Hladik F., McNevin J.P., McElrath M.J., Gale M. Human immunodeficiency virus type 1 mediates global disruption of innate antiviral signaling and immune defenses within infected cells. J. Virol. 2009, 83:10395-10405.
63. Neil S.J., Zang T., Bieniasz P.D. Tetherin inhibits retrovirus release and is antagonized by HIV-1 Vpu. Nature 2008, 451:425-430.
64. Bishop K.N., Holmes R.K., Sheehy A.M., Malim M.H. APOBEC-mediated editing of viral RNA. Science 2004, 305:645.
65. Yue Z., Shatkin A.J. Double-stranded RNA-dependent protein kinase (PKR) is regulated by reovirus structural proteins. Virology 1997, 234:364-371.
66. Romano P.R., Zhang F., Tan S.L., Garcia-Barrio M.T., Katze M.G., Dever T.E., Hinnebusch A.G. Inhibition of double-stranded RNA-dependent protein kinase PKR by vaccinia virus E3: Role of complex formation and the E3 N-terminal domain. Mol. Cell. Biol. 1998, 18:7304-7316.
67. Garaigorta U., Chisari F.V. Hepatitis C virus blocks interferon effector function by inducing protein kinase R phosphorylation. Cell Host Microbe. 2009, 6:513-522.
68. Arnaud N., Dabo S., Maillard P., Budkowska A., Kalliampakou K.I., Mavromara P., Garcin D., Hugon J., Gatignol A., Akazawa D., Wakita T., Meurs E.F. Hepatitis C virus controls interferon production through PKR activation. PLoS One 2010, 5:e10575.
69. Smith J.A., Schmechel S.C., Raghavan A., Abelson M., Reilly C., Katze M.G., Kaufman R.J., Bohjanen P.R., Schiff L.A. Reovirus induces and benefits from an integrated cellular stress response. J. Virol. 2006, 80:2019-2033.
70. Wileman T. Aggresomes and pericentriolar sites of virus assembly: Cellular defense or viral design?. Annu. Rev. Microbiol. 2007, 61:149-167.
71. Wileman T. Aggresomes and autophagy generate sites for virus replication. Science 2006, 312:875-878.
72. Liu Y., Shevchenko A., Shevchenko A., Berk A.J. Adenovirus exploits the cellular aggresome response to accelerate inactivation of the MRN complex. J. Virol 2005, 79. 14004-14016.
73. Bordeleau M.E., Cencic R., Lindqvist L., Oberer M., Northcote P., Wagner G., Pelletier J. RNA-mediated sequestration of the RNA helicase eIF4A by Pateamine A inhibits translation initiation. Chem. Biol. 2006, 13:1287-1295.
74. Mazroui R., Sukarieh R., Bordeleau M.E., Kaufman R.J., Northcote P., Tanaka J., Gallouzi I., Pelletier J. Inhibition of ribosome recruitment induces stress granule formation independently of eukaryotic initiation factor 2alpha phosphorylation. Mol. Biol. Cell 2006, 17:4212-4219.
75. Montero H., Rojas M., Arias C.F., Lopez S. Rotavirus infection induces the phosphorylation of eIF2alpha but prevents the formation of stress granules. J. Virol. 2008, 82:1496-1504.
76. Abrahamyan L.G., Chatel-Chaix L., Ajamian L., Milev M.P., Monette A., Clement J.F., Song R., Lehmann M., Desgroseillers L., Laughrea M., Boccaccio G., Mouland A.J. Novel Staufen1 ribonucleoproteins prevent formation of stress granules but favour encapsidation of HIV-1 genomic RNA. J. Cell Sci. 2010, 123:369-383.
77. Emara M.M., Brinton M.A. Interaction of TIA-1/TIAR with West Nile and dengue virus products in infected cells interferes with stress granule formation and processing body assembly. Proc. Natl. Acad. Sci. USA 2007, 104:9041-9046.
78. White J.P., Cardenas A.M., Marissen W.E., Lloyd R.E. Inhibition of cytoplasmic mRNA stress granule formation by a viral proteinase. Cell Host Microbe. 2007, 2:295-305.
79. Loschi M., Leishman C.C., Berardone N., Boccaccio G.L. Dynein and kinesin regulate stress-granule and P-body dynamics. J. Cell Sci. 2009, 122:3973-3982.
80. Tsai N.P., Tsui Y.C., Wei L.N. Dynein motor contributes to stress granule dynamics in primary neurons. Neuroscience 2009, 159:647-656.
81. Beckham C.J., Parker R. P bodies, stress granules, and viral life cycles. Cell Host Microbe. 2008, 3:206-212.
82. Kim S., Kim H.Y., Lee S., Kim S.W., Sohn S., Kim K., Cho H. Hepatitis B virus x protein induces perinuclear mitochondrial clustering in microtubule- and dynein-dependent manners. J. Virol. 2007, 81:1714-1726.
83. Boulant S., Douglas M.W., Moody L., Budkowska A., Targett-Adams P., McLauchlan J. Hepatitis C virus core protein induces lipid droplet redistribution in a microtubule- and dynein-dependent manner. Traffic 2008, 9:1268-1282.
84. Yamada M., Toba S., Takitoh T., Yoshida Y., Mori D., Nakamura T., Iwane A.H., Yanagida T., Imai H., Yu-Lee L.Y., Schroer T., Wynshaw-Boris A., Hirotsune S. mNUDC is required for plus-end-directed transport of cytoplasmic dynein and dynactins by kinesin-1. EMBO J. 2010, 29:517-531.
85. Torisawa T., Nakayama A., Furuta K., Yamada M., Hirotsune S., Toyoshima Y.Y. Functional dissection of LIS1 and NDEL1 towards understanding the molecular mechanism of cytoplasmic dynein regulation. J. Biol. Chem. 2010, 286:1959-1965.
86. Mizuno N., Toba S., Edamatsu M., Watai-Nishii J., Hirokawa N., Toyoshima Y.Y., Kikkawa M. Dynein and kinesin share an overlapping microtubule-binding site. EMBO J. 2004, 23:2459-2467.
87. de Mareuil J., Carre M., Barbier P., Campbell G.R., Lancelot S., Opi S., Esquieu D., Watkins J.D., Prevot C., Braguer D., Peyrot V., Loret E.P. HIV-1 Tat protein enhances microtubule polymerization. Retrovirology 2005, 2:5.
88. Watts N.R., Sackett D.L., Ward R.D., Miller M.W., Wingfield P.T., Stahl S.S., Steven A.C. HIV-1 rev depolymerizes microtubules to form stable bilayered rings. J. Cell Biol. 2000, 150:349-360.
89. Nejmeddine M., Barnard A.L., Tanaka Y., Taylor G.P., Bangham C.R. Human T-lymphotropic virus, type 1, tax protein triggers microtubule reorientation in the virological synapse. J. Biol. Chem. 2005, 280:29653-29660.
90. Liao Z., Cimakasky L.M., Hampton R., Nguyen D.H., Hildreth J.E. Lipid rafts and hiv pathogenesis: Host membrane cholesterol is required for infection by hiv type 1. AIDS Res. Hum. Retroviruses 2001, 17:1009-1019.
91. Thali M. The roles of tetraspanins in HIV-1 replication. Curr. Top. Microbiol. 2009, 339:85-102.
92. Levesque K., Halvorsen M., Abrahamyan L., Chatel-Chaix L., Poupon V., Gordon H., DesGroseillers L., Gatignol A., Mouland A.J. Trafficking of HIV-1 RNA is mediated by heterogeneous nuclear ribonucleoprotein A2 expression and impacts on viral assembly. Traffic 2006, 7:1177-1193.
93. Poole E., Strappe P., Mok H.P., Hicks R., Lever A.M. HIV-1 Gag-RNA interaction occurs at a perinuclear/centrosomal site; analysis by confocal microscopy and FRET. Traffic 2005, 6:741-755.
94. Lehmann M., Milev M.P., Abrahamyan L., Yao X.J., Pante N., Mouland A.J. Intracellular transport of human immunodeficiency virus type 1 genomic RNA and viral production are dependent on dynein motor function and late endosome positioning. J. Biol. Chem. 2009, 284. 14572-14585.
95. Sossin W.S., DesGroseillers L. Intracellular trafficking of RNA in neurons. Traffic 2006, 7:1581-1589.
96. Kural C., Kim H., Syed S., Goshima G., Gelfand V.I., Selvin P.R. Kinesin and dynein move a peroxisome in vivo: A tug-of-war or coordinated movement?. Science 2005, 308:1469-1472.
97. Carson J.H., Cui H., Barbarese E. The balance of power in RNA trafficking. Curr. Opin. Neurobiol. 2001, 11:558-563.
98. Progida C., Spinosa M.R., De Luca A., Bucci C. RILP interacts with the VPS22 component of the ESCRT-II complex. Biochem. Biophys. Res. Commun. 2006, 347:1074-1079.
99. Wang T., Hong W. RILP interacts with VPS22 and VPS36 of ESCRT-II and regulates their membrane recruitment. Biochem. Biophys. Res. Commun. 2006, 350:413-423.
100. Glued, ORP1L, and the receptor βlll spectrin. J. Cell Biol. 2007, 176:459-471.
101. Short B., Preisinger C., Schaletzky J., Kopajtich R., Barr F.A. The Rab6 GTPase regulates recruitment of the dynactin complex to Golgi membranes. Curr. Biol. 2002, 12:1792-1795.
102. Sfakianos J.N., LaCasse R.A., Hunter E. The M-PMV cytoplasmic targeting-retention signal directs nascent Gag polypeptides to a pericentriolar region of the cell. Traffic 2003, 4:660-670.
103. Vlach J., Lipov J., Rumlova M., Veverka V., Lang J., Srb P., Knejzlik Z., Pichova I., Hunter E., Hrabal R., Ruml T. D-retrovirus morphogenetic switch driven by the targeting signal accessibility to Tctex-1 of dynein. Proc. Natl. Acad. Sci. USA 2008, 105:10565-10570.
104. Forgues M., Difilippantonio M.J., Linke S.P., Ried T., Nagashima K., Feden J., Valerie K., Fukasawa K., Wang X.W. Involvement of Crm1 in hepatitis B virus X protein-induced aberrant centriole replication and abnormal mitotic spindles. Mol. Cell Biol. 2003, 23:5282-5292.
105. Epie N., Ammosova T., Sapir T., Voloshin Y., Lane W.S., Turner W., Reiner O., Nekhai S. HIV-1 Tat interacts with LIS1 protein. Retrovirology 2005, 2:6.
106. Jouvenet N., Wileman T. African swine fever virus infection disrupts centrosome assembly and function. J. Gen. Virol. 2005, 86:589-594.
107. Ploubidou A., Moreau V., Ashman K., Reckmann I., Gonzalez C., Way M. Vaccinia virus infection disrupts microtubule organization and centrosome function. EMBO J. 2000, 19:3932-3944.
108. Piguet V., Sattentau Q. Dangerous liaisons at the virological synapse. J. Clin. Invest. 2004, 114:605-610.
109. Vasiliver-Shamis G., Dustin M.L., Hioe C.E. HIV-1 virological synapse is not simply a copycat of the immunological synapse. Viruses 2010, 2:1239-1260.
110. Jolly C., Sattentau Q.J. Retroviral spread by induction of virological synapses. Traffic 2004, 5:643-650.
111. Nejmeddine M., Negi V.S., Mukherjee S., Tanaka Y., Orth K., Taylor G.P., Bangham C.R. HTLV-1-Tax and ICAM-1 act on T-cell signal pathways to polarize the microtubule-organizing center at the virological synapse. Blood 2009, 114:1016-1025.
112. Quann E.J., Merino E., Furuta T., Huse M. Localized diacylglycerol drives the polarization of the microtubule-organizing center in T cells. Nat. Immunol. 2009, 10:627-635.
113. Rudnicka D., Feldmann J., Porrot F., Wietgrefe S., Guadagnini S., Prevost M.C., Estaquier J., Haase A.T., Sol-Foulon N., Schwartz O. Simultaneous cell-to-cell transmission of human immunodeficiency virus to multiple targets through polysynapses. J. Virol. 2009, 83:6234-6246.
114. Pumfery A., de la Fuente C., Kashanchi F. HTLV-1 Tax: Centrosome amplification and cancer. Retrovirology 2006, 3:50.
115. Netherton C., Moffat K., Brooks E., Wileman T. A guide to viral inclusions, membrane rearrangements, factories, and viroplasm produced during virus replication. Adv. Virus Res. 2007, 70:101-182.
116. Katsafanas G.C., Moss B. Colocalization of transcription and translation within cytoplasmic poxvirus factories coordinates viral expression and subjugates host functions. Cell Host Microbe. 2007, 2:221-228.
117. Ward B.M. Visualization and characterization of the intracellular movement of vaccinia virus intracellular mature virions. J. Virol. 2005, 79:4755-4763.
118. Remillard-Labrosse G., Mihai C., Duron J., Guay G., Lippe R. Protein kinase D-dependent trafficking of the large herpes simplex virus type 1 capsids from the TGN to plasma membrane. Traffic 2009, 10:1074-1083.
119. Leopold P.L., Pfister K.K. Viral strategies for intracellular trafficking: Motors and microtubules. Traffic 2006, 7:516-523.
120. Greber U.F., Way M. A superhighway to virus infection. Cell 2006, 124:741-754.
121. Dohner K., Nagel C.H., Sodeik B. Viral stop-and-go along microtubules: Taking a ride with dynein and kinesins. Trends Microbiol. 2005, 13:320-327.
122. Henry T., Gorvel J.P., Meresse S. Molecular motors hijacking by intracellular pathogens. Cell. Microbiol. 2006, 8:23-32.
123. Gazzola M., Burckhardt C.J., Bayati B., Engelke M., Greber U.F., Koumoutsakos P. A stochastic model for microtubule motors describes the in vivo cytoplasmic transport of human adenovirus. PLoS Comput. Biol. 2009, 5:e1000623.
124. Mabit H., Nakano M.Y., Prank U., Saam B., Dohner K., Sodeik B., Greber U.F. Intact microtubules support adenovirus and herpes simplex virus infections. J. Virol. 2002, 76:9962-9971.
125. Kannan H., Fan S., Patel D., Bossis I., Zhang Y.J. The hepatitis E virus open reading frame 3 product interacts with microtubules and interferes with their dynamics. J. Virol. 2009, 83:6375-6382.
126. Dohner K., Wolfstein A., Prank U., Echeverri C., Dujardin D., Vallee R., Sodeik B. Function of dynein and dynactin in herpes simplex virus capsid transport. Mol. Biol. Cell 2002, 13:2795-2809.
127. Sodeik B., Ebersold M.W., Helenius A. Microtubule-mediated transport of incoming herpes simplex virus 1 capsids to the nucleus. J. Cell Biol. 1997, 136:1007-1021.
128. Topp K.S., Meade L.B., LaVail J.H. Microtubule polarity in the peripheral processes of trigeminal ganglion cells: Relevance for the retrograde transport of herpes simplex virus. J. Neurosci. 1994, 14:318-325.
129. Wolfstein A., Nagel C.H., Radtke K., Dohner K., Allan V.J., Sodeik B. The inner tegument promotes herpes simplex virus capsid motility along microtubules in vitro. Traffic 2006, 7:227-237.
130. Ye G.J., Vaughan K.T., Vallee R.B., Roizman B. The herpes simplex virus 1 U(L)34 protein interacts with a cytoplasmic dynein intermediate chain and targets nuclear membrane. J. Virol. 2000, 74:1355-1363.
131. Gonzalez Duran E., del Angel R.M., Salas Benito J.S. In vitro interaction of poliovirus with cytoplasmic dynein. Intervirology 2007, 50:214-218.
132. Havecker E.R., Gao X., Voytas D.F. The Sireviruses, a plant-specific lineage of the Ty1/copia retrotransposons, interact with a family of proteins related to dynein light chain 8. Plant Physiology 2005, 139:857-868.
133. Herrero-Martinez E., Roberts K.L., Hollinshead M., Smith G.L. Vaccinia virus intracellular enveloped virions move to the cell periphery on microtubules in the absence of the A36R protein. J. Gen. Virol. 2005, 86:2961-2968.