Cytoskeleton in the Parasitic Plant Cuscuta During Germination and Prehaustorium Formation
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
29971075
PubMed Central
PMC6018488
DOI
10.3389/fpls.2018.00794
Knihovny.cz E-zdroje
- Klíčová slova
- Cuscuta, actin filaments, dodder, microtubules, parasitic weeds, prehaustorium, root-like structure, shoot apical meristem,
- Publikační typ
- časopisecké články MeSH
Although cytoskeleton is a driving force for cell division and growth in higher plants, there is little evidence about its components in parasitic angiosperms. Microtubules and actin filaments in cells of shoot apical meristem and root-like structure of stem holoparasites European (C. europaea L.) and Eastern (C. monogyna Vahl.) dodders, as well as in prehaustorium, the specific organ adapted to parasitism, were visualized for the first time by immunolabeling and fluorescence microscopy. The significance of cytoskeletal elements during germination and prehaustorium formation was addressed by treatments with taxol, oryzalin, latrunculin B, cytochalasin B/D, jasplakinolide, and 2,3-butanedione monoxime. In shoot apical meristem many dividing cells were observed, in contrast to root-like structure, devoid of cell divisions. Cortical microtubules were oriented transversely and/or obliquely, while actin filaments were randomly distributed in cells of both organs. Furthermore, longitudinal cortical microtubules were present in digitate cells of prehaustorium, and transverse arrays were found in its file cells. Long and short random actin filaments were also observed in prehaustorium cells. Thus, it was shown that the cytoskeleton in dodder shoot cells is organized in a similar way to non-parasitic dicots, while cytoskeletal organization has some peculiarities in quickly senescing root-like structure and prehaustorium.
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Alakonya A., Kumar R., Koenig D., Kimura S., Townsley B., Runo S., et al. (2012). Interspecific RNA interference of PubMed DOI PMC
Baluška F., Jasik J., Edelmann H. G., Salajová T., Volkmann D. (2001). Latrunculin B-induced plant dwarfism: plant cell elongation is F-actin-dependent. PubMed DOI
Baluška F., Šamaj J., Volkmann D., Barlow P. W. (1997). Impact of taxol-mediated stabilization of microtubules on nuclear morphology, ploidy levels and cell growth in maize roots. PubMed DOI
Bartels P. G., Hilton J. L. (1973). Comparison of trifluralin, oryzalin, pronamide, propham, and colchicine treatments on microtubules. DOI
Bibikova T. N., Blancaflor E. B., Gilroy S. (1999). Microtubules regulate tip growth and orientation in root hairs of PubMed DOI
Cai C., Henty-Ridilla J. L., Szymanski D. B., Staiger C. J. (2014). Arabidopsis myosin XI: a motor rules the tracks. PubMed DOI PMC
Costea M., García M. A., Stefanović S. (2015). A phylogenetically based infrageneric classification of the parasitic plant genus DOI
Coué M., Brenner S. L., Spector I., Korn E. D. (1987). Inhibition of actin polymerization by latrunculin A. PubMed DOI
Dawson J. H., Musselman L. J., Wolswinkel P., Dörr I. (1994). Biology and control of
Dolan L., Janmaat K., Willemsen V., Linstead P., Poethig S., Roberts K., et al. (1993). Cellular organisation of the PubMed
de Almeida Engler J., Rodiuc N., Smertenko A., Abad P. (2010). Plant actin cytoskeleton remodeling by plant parasitic nematodes. PubMed DOI PMC
Estabrook E. M., Yoder J. I. (1998). Plant-plant communications: rhizosphere signaling between parasitic angiosperms and their hosts. DOI
Florea C. S., Timko M. P. (1997). Actin genes with unusual organization in the parasitic angiosperm PubMed DOI
Fukuda H., Kobayashi H. (1989). Dynamic organization of the cytoskeleton during tracheary-element differentiation. PubMed DOI
Galatis B., Apostolakos P. (2004). The role of the cytoskeleton in the morphogenesis and function of stomatal complexes. PubMed DOI
García M. A., Costea M., Kuzmina M., Stefanović S. (2014). Phylogeny, character evolution, and biogeography of PubMed DOI
Gibbon B. C., Kovar D. R., Staiger C. J. (1999). Latrunculin B has different effects on pollen germination and tube growth. PubMed DOI PMC
Gutierrez R., Lindeboom J. J., Paredez A. R., Emons A. M. C., Ehrhardt D. W. (2009). PubMed DOI
Henty-Ridilla J. L., Li J., Blanchoin L., Staiger C. J. (2013). Actin dynamics in the cortical array of plant cells. PubMed DOI
Hoffman J. C., Vaughn K. C. (1994). Mitotic disrupter herbicides act by a single mechanism but vary in efficacy. DOI
Hoffmann A., Nebenführ A. (2004). Dynamic rearrangements of transvacuolar strands in BY-2 cells imply a role of myosin in remodeling the plant actin cytoskeleton. PubMed DOI
Holzinger A., Blaas K. (2016). Actin-dynamics in plant cells: the function of actin perturbing substances jasplakinolide, chondramides, phalloidin, cytochalasins, and latrunculins. PubMed DOI PMC
Kaštier P., Martinčová M., Fiala R., Blehová A. (2017). Transient expression of green fluorescent protein in parasitic dodder as a tool for studying of cytoskeleton. DOI
Khatau S. B., Hale C. M., Stewart-Hutchinson P. J., Patel M. S., Stewart C. L., Searson P. C., et al. (2009). A perinuclear actin cap regulates nuclear shape. PubMed DOI PMC
Kim G., Westwood J. H. (2015). Macromolecule exchange in PubMed DOI
Kost B., Bao Y.-Q., Chua N.-H. (2002). Cytoskeleton and plant organogenesis. PubMed DOI PMC
Kuijt J., Toth R. (1976). Ultrastructure of angiosperm haustoria—a review. DOI
Lapin D., Van den Ackerveken G. (2013). Susceptibility to plant disease: more than a failure of host immunity. PubMed DOI
Lee K. B. (2007). Structure and development of the upper haustorium in the parasitic flowering plant PubMed DOI
Lee K. B., Park J.-B., Lee S. (2000). Morphology and anatomy of mature embryos and seedlings in parasitic angiosperm DOI
Lee R. Q., Lee K. F. (1989). Parasitic Size and superstrate effects on electromagnetic coupled patch antennas. DOI
Lyshede O. B. (1985). Morphological and anatomical features of DOI
Lyshede O. B. (1986). Fine-structural features of the tuberous radicular end of the seedling of DOI
Mao G., Buschmann H., Doonan J. H., Lloyd C. W. (2006). The role of MAP65-1 in microtubule bundling during PubMed DOI
Mathur J., Chua N. H. (2000). Microtubule stabilization leads to growth reorientation in Arabidopsis trichomes. PubMed DOI PMC
Mathur J., Hülskamp M. (2002). Microtubules and microfilaments in cell morphogenesis in higher plants. PubMed DOI
Morejohn L. C., Bureau T. E., Molè-Bajer J., Bajer A. S., Fosket D. E. (1987). Oryzalin, a dinitroaniline herbicide, binds to plant tubulin and inhibits microtubule polymerization PubMed DOI
Murashige T., Skoog F. (1962). A Revised medium for rapid growth and bio assays with tobacco tissue cultures. DOI
Oda Y., Mimura T., Hasezawa S. (2005). Regulation of secondary cell wall development by cortical microtubules during tracheary element differentiation in Arabidopsis cell suspensions. PubMed DOI PMC
Panteris E., Apostolakos P., Galatis B. (2006). Cytoskeletal asymmetry in PubMed DOI
Pesquet E., Korolev A. V., Calder G., Lloyd C. W. (2010). The microtubule-associated protein AtMAP70-5 regulates secondary wall patterning in PubMed DOI
Šamaj J., Ovecka M., Hlavacka A., Lecourieux F., Meskiene I., Lichtscheidl I., et al. (2002). Involvement of the mitogen-activated protein kinase SIMK in regulation of root hair tip growth. PubMed DOI PMC
Šamaj J., Peters M., Volkmann D., Baluška F. (2000). Effects of myosin ATPase inhibitor 2,3-butanedione 2-monoxime on distributions of myosins, F-actin, microtubules, and cortical endoplasmic reticulum in maize root apices. PubMed DOI
Šamajová O., Komis G., Šamaj J. (2014). PubMed DOI
Saric-Krsmanovic M. M., Bozic D. M., Radivojevic L. M., Umiljendic J. S. G., Vrbnicanin S. P. (2017). Effect of PubMed DOI
Sasaki T., Fukuda H., Oda Y. (2017). CORTICAL MICROTUBULE DISORDERING1 is required for secondary cell wall patterning in xylem vessels. PubMed DOI PMC
Schmidt S. M., Panstruga R. (2007). Cytoskeleton functions in plant–microbe interactions. DOI
Sherman T. D., Bowling A. J., Barger T. W., Vaughn K. C. (2008). The vestigial root of dodder ( DOI
Smertenko A., Assaad F., Baluška F., Bezanilla M., Buschmann H., Drakakaki G., et al. (2017). Plant cytokinesis: terminology for structures and processes. PubMed DOI
Spector I., Braet F., Shochet N. R., Bubb M. R. (1999). New anti-actin drugs in the study of the organization and function of the actin cytoskeleton. PubMed DOI
Srivastava S., Nighojkar A., Kumar A. (1994). Multiple forms of pectin methylesterase from DOI
Svubova R., Lukacova Z., Kastier P., Blehova A. (2017). New aspects of dodder–tobacco interactions during haustorium development. DOI
Takemoto D., Hardham A. R. (2004). The cytoskeleton as a regulator and target of biotic interactions in plants. PubMed DOI PMC
Těšitel J. (2016). Functional biology of parasitic plants: a review. DOI
Tian J., Han L., Feng Z., Wang G., Liu W., Ma Y., et al. (2015). Orchestration of microtubules and the actin cytoskeleton in trichome cell shape determination by a plant-unique kinesin. PubMed DOI PMC
Toma C., Andronache A., Toma I. (2005). Histo-anatomical investigations on some
van der Kooij T. A., Krause K., Dörr I., Krupinska K. (2000). Molecular, functional and ultrastructural characterisation of plastids from six species of the parasitic flowering plant genus PubMed DOI
Vaughn K. C. (2002). Attachment of the parasitic weed dodder to the host. PubMed DOI
Vaughn K. C. (2003). Dodder hyphae invade the host: a structural and immunocytochemical characterization. PubMed DOI
Vaughn K. C. (2006). Conversion of the searching hyphae of dodder into xylic and phloic hyphae: a cytochemical and immunocytochemical investigation. DOI
Vitha S., Baluška F., Jasik J., Volkmann D., Barlow P. W. (2000). DOI
Wani M. C., Horwitz S. B. (2014). Nature as a remarkable chemist: a personal story of the discovery and development of Taxol. PubMed DOI PMC
Wasteneys G. O., Ambrose J. C. (2009). Spatial organization of plant cortical microtubules: close encounters of the 2D kind. PubMed DOI
Weed Seeds Order (2016).
Yoder J. I., Scholes J. D. (2010). Host plant resistance to parasitic weeds; recent progress and bottlenecks. PubMed DOI
Yoshida S., Cui S., Ichihashi Y., Shirasu K. (2016). The haustorium, a specialized invasive organ in parasitic plants. PubMed DOI