Alzhanova, D.V., Napuli, A.J., Creamer, R. and Dolja, V.V. (2001)
Cell-to-cell movement and assembly of a plant closterovirus: roles for the
capsid proteins and Hsp70 homolog. EMBO J. 20, 6997–7007.
Aoki, K., Kragler, F., Xoconostle-Cázares, B. and Lucas, W.J. (2002) A
subclass of plant heat shock cognate 70 chaperones carries a motif that
facilitates trafficking through plasmodesmata. Proc. Natl. Acad. Sci. USA,
99, 16 342–16 347.
Aparicio, F., Thomas, C.L., Lederer, C., Niu, Y., Wang, D.W. and Maule,
A.J. (2005) Virus induction of heat shock protein 70 reflects a general
response to protein accumulation in the plant cytosol. Plant Physiol. 138,
529–536.
Aranda, M. and Maule, A. (1998) Virus-induced host gene shut off in
animals and plants. Virology, 243, 261–267.
Aranda, M.A., Escaler, M., Wang, D. and Maule, A.J. (1996) Induction
of HSP70 and polyubiquitin expression associated with plant virus
replication. Proc. Natl. Acad. Sci. USA, 93, 15 289–15 293.
von Bargen, S., Salchert, K., Paape, M., Piechulla, B. and Kellmann, J.W.
(2001) Interactions between the tomato spotted wilt virus movement
protein and plant proteins showing homologies to myosin, kinesin and
DnaJ-like chaperones. Plant Physiol. Biochem. 39, 1083–1093.
Boevink, P. and Oparka, K.J. (2005) Virus–host interactions during
movement processes. Plant Physiol. 138, 1815–1821.
Bradford, M.M. (1976) A rapid and sensitive method for the quantitation
of microgram quantities of protein utilizing the principle of protein–dye
binding. Anal. Biochem. 72, 248–254.
Broquet, A.H., Lenoir, C., Gardet, A., Sapin, C., Chwetzoff, S., Jouniaux, A-M.,
Lopez, S., Trugnan, G., Bachelet, M. and Thomas, G. (2007) Hsp70
negatively controls rotavirus protein bioavailability in Caco-2 cells
infected by the rotavirus RF strain. J. Virol. 81, 1297–1304.
Chapman, S., Kavanagh, T. and Baulcombe, D. (1992) Potato virus X as
a vector for gene expression in plants. Plant J. 2, 549–557.
Chromy, L.R., Pipas, J.M. and Garcea, R.L. (2003) Chaperone-mediated
in vitro assembly of polyomavirus capsids. Proc. Natl. Acad. Sci. USA,
100, 10 477–10 482.
Daugaard, M., Rohde, M. and Jäättelä, M. (2007) The heat shock
protein 70 family: highly homologous proteins with overlapping and
distinct functions. FEBS Lett. 581, 3702–3710.
Dufresne, P.J., Thivierge, K., Cotton, S., Beauchemin, C., Ide, C.,
Ubalijoro, E., Laliberté, J-F. and Fortin, M.G. (2008) Heat shock 70
protein interaction with Turnip mosaic virus RNA-dependent RNA polymerase
within virus-induced membrane vesicles. Virology, 374, 217–227.
Escaler, M., Aranda, M.A., Thomas, C.L. and Maule, A.J. (2000) Pea
embryonic tissues show common responses to the replication of a wide
range of viruses. Virology, 267, 318–325.
Glotzer, J.B., Saltik, M., Chiocca, S., Michou, A.I., Moseley, P. and
Cotten, M. (2000) Activation of heat-shock response by an adenovirus
is essential for virus replication. Nature, 407, 207–211.
Hartl, F.U. (1996) Molecular chaperones in cellular protein folding. Nature,
381, 571–579.
Hofius, D., Maier, A.T., Dietrich, C., Jungkunz, I., Börnke, F., Maiss, E.
and Sonnewald, U. (2007) Capsid protein-mediated recruitment of host
DnaJ-like proteins is required for Potato virus Y infection in tobacco
plants. J. Virol. 81, 11 870–11 880.
Jia, H.G., Pang, Y.Q. and Fang, R.X. (2003) Agroinoculation as a simple
way to deliver a Tobacco mosaic virus-based expression vector. Acta Bot.
Sin. 45, 770–773.
Jockusch, H., Wiegand, C., Mersch, B. and Rajes, D. (2001) Mutants of
Tobacco mosaic virus with temperature-sensitive coat proteins induce
heat shock response in tobacco leaves. Mol. Plant–Microbe Interact. 14,
914–917.
Kanzaki, H., Saitoh, H., Ito, A., Fujisawa, S., Kamoun, S., Katou, S.,
Yoshioka, H. and Terauchi, R. (2003) Cytosolic HSP90 and HSP70 are
essential components of INF1-mediated hypersensitive response and
non-host resistance to Pseudomonas cichorii in Nicotiana benthamiana.
Mol. Plant Pathol. 4, 383–391.
Koenig, R. (1981) Indirect ELISA methods for the broad specificity detection of
plant viruses. J. Gen. Virol. 55, 53–62.
Lee, J.H. and Schöffl, F. (1996) An Hsp70 antisense gene affects the
expression of HSP70/HSC70, the regulation of HSF, and the acquisition of
thermotolerance in transgenic Arabidopsis thaliana. Mol. Gen. Genet.
252, 11–19.
Maule, A.J., Escaler, M. and Aranda, M.A. (2000) Programmed
responses to virus replication in plants. Mol. Plant Pathol. 1, 9–15.
Mayer, M.P. and Bukau, B. (2005) Hsp70 chaperones: cellular functions
and molecular mechanism. Cell. Mol. Life Sci. 62, 670–684.
Medina, V., Peremyslov, V.V., Hagiwara, Y. and Dolja, V.V. (1999)
Subcellular localization of the HSP70-homolog encoded by Beet yellows
closterovirus. Virology, 260, 173–181.
Noël, L.D., Cagna, G., Stuttmann, J., Wirthmüller, L., Betsuyaku, S.,
Witte, C.-P., Bhat, R., Pochon, N., Colby, T. and Parker, J.E. (2007)
Interaction between SGT1 and cytosolic/nuclear HSC70 chaperones
regulates Arabidopsis immune responses. Plant Cell, 19, 4061–4076.
Oglesbee, M.J., Liu, Z., Kenney, H. and Brooks, C.L. (1996) The highly
inducible member of the 70 kDa family of heat shock proteins increases
canine distemper virus polymerase activity. J. Gen. Virol. 77, 2125–2135.
Peremyslov, V.V., Hagiwara, Y. and Dolja, V.V. (1999) HSP70 homolog
functions in cell-to-cell movement of a plant virus. Proc. Natl. Acad. Sci.
USA, 96, 14 771–14 776.
Prokhnevsky, A.I., Peremyslov, V.V., Napuli, A.J. and Dolja, V.V. (2002)
Interaction between long-distance transport factor and Hsp70-related
movement protein of Beet yellows virus. J. Virol. 76, 11 003–11 011.
Reyes-del Valle, J., Chávez-Salinas, S., Medina, F. and del Angel, R.M.
(2005) Heat shock protein 90 and heat shock protein 70 are components
of Dengue virus receptor complex in human cells. J. Virol. 79, 4557–4567.
Senthil, G., Liu, H., Puram, V.G., Clark, A., Stromberg, A. and Goodin,
M.M. (2005) Specific and common changes in Nicotiana benthamiana
gene expression in response to infection by enveloped viruses. J. Gen.
Virol. 86, 2615–2625.
Senthil-Kumar, M., Govind, G., Kang, L., Mysore, K.S. and Udayakumar, M.
(2007) Functional characterization of Nicotiana benthamiana homologs
of peanut water deficit-induced genes by virus-induced gene silencing.
Planta, 225, 523–539.
Serva, S. and Nagy, P.D. (2006) Proteomics analysis of the tombusvirus
replicase: Hsp70 molecular chaperone is associated with the replicase
and enhances viral RNA replication. J. Virol. 80, 2162–2169.
Su, P.H. and Li, H.M. (2008) Arabidopsis stromal 70-kD heat shock
proteins are essential for plant development and important for thermotolerance
of germinating seeds. Plant Physiol. 146, 1231–1241.
Sung, D.Y. and Guy, C.L. (2003) Physiological and molecular assessment
of altered expression of Hsc70-1 in Arabidopsis. Evidence for pleiotropic
consequences. Plant Physiol. 132, 979–987.
Sung, D.Y., Vierling, E. and Guy, C.L. (2001) Comprehensive expression
profile analysis of the Arabidopsis Hsp70 gene family. Plant Physiol. 126,
789–800.
Tomita, Y., Mizuno, T., Díez, J., Naito, S., Ahlquist, P. and Ishikawa, M.
(2003) Mutation of host dnaJ homolog inhibits Brome mosaic virus
negative-strand RNA synthesis. J. Virol. 77, 2990–2997.
Walter, M., Chaban, C., Schütze, K., Batistic, O., Weckermann, K.,
Näke, C., Blazevic, D., Grefen, C., Schumacher, K., Oecking, C.,
Harter, K. and Kudla, J. (2004) Visualization of protein interactions in
living plant cells using bimolecular fluorescence complementation. Plant
J. 40, 428–438.
Wang, W., Vinocur, B., Shoseyov, O. and Altman, A. (2004) Role of plant
heat-shock proteins and molecular chaperones in the abiotic stress
response. Trends Plant Sci. 9, 244–252.
van Wezel, R., Liu, H., Tien, P., Stanley, J. and Hong, Y. (2001) Gene C2
of the monopartite geminivirus Tomato yellow leaf curl virus-China
encodes a pathogenicity determinant that is localized in the nucleus.
Mol. Plant–Microbe Interact. 14, 1125–1128.
Whitham, S.A. and Wang, Y.Z. (2004) Roles for host factors in plant viral
pathogenicity. Curr. Opin. Plant Biol. 7, 365–371.
Whitham, S.A., Quan, S., Chang, H.S., Cooper, B., Estes, B., Zhu, T.,
Wang, X. and Hou, Y.M. (2003) Diverse RNA viruses elicit the expression
of common sets of genes in susceptible Arabidopsis thaliana plants.
Plant J. 33, 271–283.
Wroblewski, T., Tomczak, A. and Michelmore, R. (2005) Optimization
of Agrobacterium-mediated transient assays of gene expression in
lettuce, tomato and Arabidopsis. Plant Biotechnol. J. 3, 259–273.