Page:Cell-to-Cell Communication During Plant-Pathogen Interaction.pdf/10

From Wikisource
Jump to navigation Jump to search
This page has been proofread, but needs to be validated.

Peña, C. G., Snetselaar, K., McCann, M., Pérez-Martín, J., Feldbrügge, M., Basse, C. W., Steinberg, G., Ibeas, J. I., Holloman, W., Guzman, P., Farman, M., Stajich, J. E., Sentandreu, R., González-Prieto, J. M., Kennell, J. C., Molina, L., Schirawski, J., Mendoza-Mendoza, A., Greilinger, D., Münch, K., Rössel, N., Scherer, M., Vranēs, M., Ladendorf, O., Vincon, V., Fuchs, U., Sandrock, B., Meng, S., Ho, E. C. H., Cahill, M. J., Boyce, K. J., Klose, J., Klosterman, S. J., Deelstra, H. J., Ortiz-Castellanos, L., Li, W., Sanchez-Alonso, P., Schreier, P. H., Häuser-Hahn, I., Vaupel, M., Koopmann, E., Friedrich, G., Voss, H., Schlüter, T., Margolis, J., Platt, D., Swimmer, C., Gnirke, A., Chen, F., Vysotskaia, V., Mannhaupt, G., Güldener, U., Münsterkötter, M., Haase, D., Oesterheld, M., Mewes, H. W., Mauceli, E. W., DeCaprio, D., Wade, C. M., Butler, J., Young, S., Jaffe, D. B., Calvo, S., Nusbaum, C., Galagan, J., and Birren, B. W. 2006. Insights from the genome of the biotrophic fungal plant pathogen Ustilago maydis. Nature 444:97-101.

  • Kankanala, P., Czymmek, K., and Valent, B. 2007. Roles for rice membrane dynamics and plasmodesmata during biotrophic invasion by the blast fungus. Plant Cell 19:706-724.
  • Kaplan, I. B., Zhang, L., and Palukaitis, P. 1998. Characterization of cucumber mosaic virus: V. Cell-to-cell movement requires capsid protein but not virions. Virology 246:221-231.
  • Kazan, K., and Manners, J. M. 2009. Linking development to defense: Auxin in plant-pathogen interactions. Trends Plant Sci. 14:373-382.
  • Kehr, J., and Buhtz, A. 2008. Long distance transport and movement of RNA through the phloem. J. Exp. Bot. 59:85-92.
  • Khang, C. H., Berruyer, R., Giraldo, M. C., Kankanala, P., Park, S. Y., Czymmek, K., Kang, S., and Valent, B. 2010. Translocation of Magnaporthe oryzae effectors into rice cells and their subsequent cell-to-cell movement. Plant Cell 22:1388-1403.
  • Kitagawa, M., Tomoi, T., Fukushima, T., Sakata, Y., Sato, M., Toyooka, K., Fujita, T., and Sakakibara, H. 2019. Abscisic acid acts as a regulator of molecular trafficking through plasmodesmata in the moss Physcomitrella patens. Plant Cell Physiol. 60:738-751.
  • Kunze, G., Zipfel, C., Robatzek, S., Niehaus, K., Boller, T., and Felix, G. 2004. The N terminus of bacterial elongation factor Tu elicits innate immunity in Arabidopsis plants. Plant Cell 16:3496-3507.
  • Kwiatkowska, M. 1991. Autoradiographic studies on the role of plasmodesmata in the transport of gibberellin. Planta 183:294-299.
  • Lee, J. Y., and Frank, M. 2018. Plasmodesmata in phloem: Different gateways for different cargoes. Curr. Opin. Plant Biol. 43:119-124.
  • Lee, J.-Y., and Lu, H. 2011. Plasmodesmata: The battleground against intruders. Trends Plant Sci. 16:201-210.
  • Lee, J. Y., Wang, X., Cui, W., Sager, R., Modla, S., Czymmek, K., Zybaliov, B., Van Wijk, K., Zhang, C., Lu, H., and Lakshmanana, V. 2011. A plasmodesmata-localized protein mediates crosstalk between cell-to-cell communication and innate immunity in Arabidopsis. Plant Cell 23:3353-3373.
  • Lee, M. W., Jelenska, J., and Greenberg, J. T. 2008. Arabidopsis proteins important for modulating defense responses to Pseudomonas syringae that secrete HopW1-1. Plant J. 54:452-465.
  • Lewis, J. D., Guttman, D. S., and Desveaux, D. 2009. The targeting of plant cellular systems by injected type III effector proteins. Semin. Cell Dev. Biol. 20:1055-1063.
  • Li, Q., Zheng, J., Li, S., Huang, G., Skilling, S. J., Wang, L., Li, L., Li, M., Yuan, L., and Liu, P. 2017. Transporter-mediated nuclear entry of jasmonoyl-isoleucine is essential for jasmonate signaling. Mol. Plant 10:695-708.
  • Li, T., Lei, W., He, R., Tang, X., Han, J., Zou, L., Yin, Y., Lin, H., and Zhang, D. 2020. Brassinosteroids regulate root meristem development by mediating BIN2-UPB1 module in Arabidopsis. PLoS Genet. 16:e1008883.
  • Li, Z., Variz, H., Chen, Y., Liu, S.-L., and Aung, K. 2021. Plasmodesmata-dependent intercellular movement of bacterial effectors. Front. Plant Sci. 12:464.
  • Lim, G. H., Liu, H., Yu, K., Liu, R., Shine, M. B., Fernandez, J., Burch-Smith, T., Mobley, J. K., McLetchie, N., Kachroo, A., and Kachroo, P. 2020. The plant cuticle regulates apoplastic transport of salicylic acid during systemic acquired resistance. Sci. Adv. 6:eaaz0478.
  • Lim, G. H., Shine, M. B., De Lorenzo, L., Yu, K., Cui, W., Navarre, D., Hunt, A. G., Lee, J. Y., Kachroo, A., and Kachroo, P. 2016. Plasmodesmata localizing proteins regulate transport and signaling during systemic acquired immunity in plants. Cell Host Microbe 19:541-549.
  • Liu, S. R., Zhou, J. J., Hu, C. G., Wei, C. L., and Zhang, J. Z. 2017. MicroRNA-mediated gene silencing in plant defense and viral counter-defense. Front. Microbiol. 8:1801.
  • Lucas, W. J., and Lee, J. Y. 2004. Plasmodesmata as a supracellular control network in plants. Nat. Rev. Mol. Cell Biol. 5:712-726.
  • Mao, G., Meng, X., Liu, Y., Zheng, Z., Chen, Z., and Zhang, S. 2011. Phosphorylation of a WRKY transcription factor by two pathogen-responsive MAPKs drives phytoalexin biosynthesis in Arabidopsis. Plant Cell 23:1639-1653.
  • Meng, L., Wong, J. H., Feldman, L. J., Lemaux, P. G., and Buchanan, B. B. 2010. A membrane-associated thioredoxin required for plant growth moves from cell to cell, suggestive of a role in intercellular communication. Proc. Natl. Acad. Sci. U.S.A. 107:3900-3905.
  • Miedes, E., Vanholme, R., Boerjan, W., and Molina, A. 2014. The role of the secondary cell wall in plant resistance to pathogens. Front. Plant Sci. 5:358.
  • Mielke, K., Forner, S., Kramell, R., Conrad, U., and Hause, B. 2011. Cell-specific visualization of jasmonates in wounded tomato and Arabidopsis leaves using jasmonate-specific antibodies. New Phytol. 190:1069-1080.
  • Mine, A., Berens, M. L., Nobori, T., Anver, S., Fukumoto, K., Winkelmüller, T. M., Takeda, A., Becker, D., and Tsuda, K. 2017. Pathogen exploitation of an abscisic acid- and jasmonate-inducible MAPK phosphatase and its interception by Arabidopsis immunity. Proc. Natl. Acad. Sci. U.S.A. 114:7456-7461.
  • Mittag, T., and Strader, L. C. 2020. I will survive: How NPR1 condensation promotes plant cell survival. Cell 182:1072-1074.
  • Morozov, S. Y., and Solovyev, A. G. 2003. Triple gene block: Modular design of a multifunctional machine for plant virus movement. J. Gen. Virol. 84:1351-1366.
  • Muhammad, T., Zhang, F., Zhang, Y., and Liang, Y. 2019. RNA interference: A natural immune system of plants to counteract biotic stressors. Cells 8:38.
  • Murillo, I., Cavallarin, L., and San Segundo, B. 1997. The maize pathogenesis-related PRms protein localizes to plasmodesmata in maize radicles. Plant Cell 9:145-156.
  • Nakajima, K., Sena, G., Nawy, T., and Benfey, P. N. 2001. Intercellular movement of the putative transcription factor SHR in root patterning. Nature 413:307-311.
  • Nakano, M., and Mukaihara, T. 2019. Comprehensive identification of PTI suppressors in type III effector repertoire reveals that Ralstonia solanacearum activates jasmonate signaling at two different steps. Int. J. Mol. Sci. 20:5992.
  • Naseem, M., Kaltdorf, M., and Dandekar, T. 2015. The nexus between growth and defence signalling: Auxin and cytokinin modulate plant immune response pathways. J. Exp. Bot. 66:4885-4896.
  • Navarro, L., Bari, R., Achard, P., Lisón, P., Nemri, A., Harberd, N. P., and Jones, J. D. G. 2008. DELLAs control plant immune responses by modulating the balance of jasmonic acid and salicylic acid signaling. Curr. Biol. 18:650-655.
  • Ngou, B. P. M., Ahn, H. K., Ding, P., and Jones, J. D. G. 2020. Mutual potentiation of plant immunity by cell-surface and intracellular receptors. bioRxiv 10.034173.
  • Nomura, K., Mecey, C., Lee, Y. N., Imboden, L. A., Chang, J. H., and He, S. Y. 2011. Effector-triggered immunity blocks pathogen degradation of an immunity-associated vesicle traffic regulator in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 108:10774-10779.
  • O’Brien, J. A., Daudi, A., Butt, V. S., and Bolwell, G. P. 2012. Reactive oxygen species and their role in plant defence and cell wall metabolism. Planta 236:765-779.
  • Ormenese, S., Bernier, G., and Périlleux, C. 2006. Cytokinin application to the shoot apical meristem of Sinapis alba enhances secondary plasmodesmata formation. Planta 224:1481-1484.
  • Osbourn, A. E. 1996. Preformed antimicrobial compounds and plant defense against fungal attack. Plant Cell 8:1821-1831.
  • Pike, S. M., Zhang, X. C., and Gassmann, W. 2005. Electrophysiological characterization of the Arabidopsis avrRpt2-specific hypersensitive response in the absence of other bacterial signals. Plant Physiol. 138:1009-1017.
  • Qi, J., Wang, J., Gong, Z., and Zhou, J. M. 2017. Apoplastic ROS signaling in plant immunity. Curr. Opin. Plant Biol. 38:92-100.
  • Qi, L., Yan, J., Li, Y., Jiang, H., Sun, J., Chen, Q., Li, H., Chu, J., Yan, C., Sun, X., Yu, Y., Li, C., and Li, C. 2012. Arabidopsis thaliana plants differentially modulate auxin biosynthesis and transport during defense responses to the necrotrophic pathogen Alternaria brassicicola. New Phytol. 195:872-882.
  • Ranathunge, K., Steudle, E., and Lafitte, R. 2005. Blockage of apoplastic bypass-flow of water in rice roots by insoluble salt precipitates analogous to a Pfeffer cell. Plant Cell Environ. 28:121-133.
  • Rinne, P. L. H., Kaikuranta, P. M., and Der Van Schoot, C. 2001. The shoot apical meristem restores its symplasmic organization during chilling-induced release from dormancy. Plant J. 26:249-264.
Vol. 35, No. 2, 2022 / 107