Epigenetic Memory as a Basis for Intelligent Behavior in Clonal Plants

. 2016 ; 7 () : 1354. [epub] 20160831

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid27630664

Environmentally induced epigenetic change enables plants to remember past environmental interactions. If this memory capability is exploited to prepare plants for future challenges, it can provide a basis for highly sophisticated behavior, considered intelligent by some. Against the backdrop of an overview of plant intelligence, we hypothesize: (1) that the capability of plants to engage in such intelligent behavior increases with the additional level of complexity afforded by clonality, and; (2) that more faithful inheritance of epigenetic information in clonal plants, in conjunction with information exchange and coordination between connected ramets, is likely to enable especially advanced intelligent behavior in this group. We therefore further hypothesize that this behavior provides ecological and evolutionary advantages to clonal plants, possibly explaining, at least in part, their widespread success. Finally, we suggest avenues of inquiry to enable assessing intelligent behavior and the role of epigenetic memory in clonal species.

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Addicott F. T. (1982).

Alpert P., Stuefer J. F. (1997). “Division of labour in clonal plants,” in

Alvarez M. E., Nota F., Cambiagno D. A. (2010). Epigenetic control of plant immunity. PubMed DOI PMC

Bell A. D. (1984). “Dynamic morphology: a contribution to plant population ecology,” in

Bilichak A., Ilnystkyy Y., Hollunder J., Kovalchuk I. (2012). The progeny of PubMed DOI PMC

Bird A. (2007). Perceptions of epigenetics. PubMed DOI

Bonabeau E., Dorigo M., Theraulaz G. (1999).

Boyko A., Blevins T., Yao Y., Golubov A., Bilichak A., Ilnytskyy Y., et al. (2010). Transgenerational adaptation of PubMed DOI PMC

Bruce T. J. A., Matthes M. C., Napier J. A., Pickett J. A. (2007). Stressful ‘memories’ of plants: evidence and possible mechanisms. DOI

Chaves M. M., Maroco J. P., Pereira J. S. (2003). Understanding plant responses to drought—from genes to the whole plant. PubMed DOI

Chinnusamy V., Zhu J. K. (2009). Epigenetic regulation of stress responses in plants. PubMed DOI PMC

Cortijo S., Wardenaar R., Colomé-Tatché M., Gilly A., Etcheverry M., Labadie K., et al. (2014). Mapping the epigenetic basis of complex traits. PubMed DOI

Darwin C. (1880).

Ding Y., Fromm M., Avramova Z. (2012). Multiple exposures to drought “train” transcriptional responses in PubMed DOI

Falik O., Mordoch Y., Quansah L., Fait A., Novoplansky A. (2011). Rumor has it…: relay communication of stress cues in plants. PubMed DOI PMC

Firn R. (2004). Plant intelligence: an alternative point of view. PubMed DOI PMC

Fischer M., Stöcklin J. (1997). Local extinctions of plants in remnants of extensively used calcareous grasslands 1950–1985. DOI

Gagliano M., Renton M., Depczynski M., Mancuso M. (2014). Experience teaches plants to learn faster and forget slower in environments where it matters. PubMed DOI

Galloway L. F., Etterson J. R. (2007). Transgenerational plasticity is adaptive in the wild. PubMed DOI

Ginsburg S., Jablonka E. (2009). Epigenetic learning in non-neural organisms. PubMed DOI

Gómez S., Latzel V., Verhulst Y., Stuefer J. F. (2007). Costs and benefits of induced resistance in a clonal plant network. PubMed DOI PMC

Griffiths M., McIntyre H. C. H. (1993). The interrelationship of growth and frost tolerance in winter rye. DOI

Ishikawa H., Hasenstein K. H., Evans M. L. (1991). Computer-based video digitizer analysis of surface extension in maize roots. PubMed DOI

Jablonka E., Lamb M. J. (1995).

Jablonka E., Lamb M. J. (2005).

Johannes F., Porcher E., Teixeira F. K., Saliba-Colombani V., Simon M., Agier N., et al. (2009). Assessing the impact of transgenerational epigenetic variation on complex traits. PubMed DOI PMC

Karpinski S., Szechynska-Hebda M. (2010). Secret life of plants: from memory to intelligence. PubMed DOI PMC

Kemperman J. A., Barnes B. V. (1976). Clone size in American aspens. DOI

Klimeš L., Klimešová J., Hendriks R., van Groenendael J. (1997). “Clonal plant architecture: a comparative analysis of form and function,” in

Kou H., Li Y., Song X., Ou X., Xing S., Ma J., et al. (2011). Heritable alteration in DNA methylation induced by nitrogen-deficiency stress accompanies enhanced tolerance by progenies to the stress in rice ( PubMed DOI

Kozlowski T. T., Pallardy S. G. (2002). Acclimation and adaptive responses of woody plants to environmental stresses. DOI

Latzel V., Janeček Š., Doležal J., Klimešová J., Bossdorf O. (2014). Adaptive transgenerational plasticity in the perennial

Latzel V., Klimešová J. (2010). Transgenerational plasticity in clonal plants. DOI

Latzel V., Klimešová J., Hájek T., Gómez S., Šmilauer P. (2010). Maternal effects alter progeny’s response to disturbance and nutrients in two DOI

Latzel V., Zhang Y. Y., Moritz K. K., Fischer M., Bossdorf O. (2012). Epigenetic variation in plant responses to defence hormones. PubMed DOI PMC

Liu B., Wendel J. F. (2003). Epigenetic phenomena and the evolution of plant allopolyploids. PubMed DOI

Louapre P., Bittebiere A., Clément B., Pierre J., Mony C. (2012). How past and present influence the foraging of clonal plants? PubMed DOI PMC

Molinier J., Ries G., Zipfel C., Hohn B. (2006). Transgeneration memory of stress in plants. PubMed DOI

Müller-Xing R., Xing Q., Goodrich J. (2014). Footprints of the sun: memory of UV and light stress in plants. PubMed DOI PMC

Novoplansky A. (2016). “Future perception in plants,” in DOI

Paszkowski J., Grossniklaus U. (2011). Selected aspects of transgenerational epigenetic inheritance and resetting in plants. PubMed DOI

Raj S., Bräutigam K., Hamanishi E. T., Wilkins O., Thomas B. R., Schroeder W., et al. (2011). Clone history shapes PubMed DOI PMC

Rendina González A. P., Chrtek J., Dobrev P. I., Dumalasová V., Fehrer J., Mráz P.et al. (in press). Stress-induced memory alters growth of clonal offspring of white clover ( PubMed DOI

Richards C. L., Schrey A. W., Pigliucci M. (2012). Invasion of diverse habitats by few Japanese knotweed genotypes is correlated with epigenetic differentiation. PubMed DOI

Shemesh H., Ovadia O., Novoplansky O. (2010). Anticipating future conditions via trajectory sensitivity. PubMed DOI PMC

Shen-Miller J. (1973). Rhythmic differences in the basipetal movement of indole-acetic acid between separated upper and lower halves of geotropically stimulated corn coleoptiles. PubMed DOI PMC

Stenhouse D. (1974).

Stuefer J. F., Gómez S., Van Mölken T. (2004). Clonal integration beyond resource sharing: implications for defence signalling and disease transmission in clonal plant networks. DOI

Stuefer J. F., Hutchings M. J. (1994). Environmental heterogeneity and clonal growth: a study of the capacity for reciprocal translocation in PubMed DOI

Sultan S. E., Barton K., Wilczek A. M. (2009). Contrasting patterns of transgenerational plasticity in ecologically distinct congeners. PubMed DOI

Szechynska-Hebda M., Kruk J., Gorecka M., Karpinska B., Karpinski S. (2010). Evidence for light wavelength-specific systemic photoelectrophysiological signaling and cellular light memory of excess light episode in PubMed DOI PMC

Takayama S., Sakagami Y. (2002). Peptide signaling in plants. PubMed DOI

Tatra G. S., Miranda J., Chinnappa C. C., Reid D. M. (2000). Effect of light quality and 5-azacytidine on genomic methylation and stem elongation in two ecotypes of DOI

Thellier M., Lüttge U. (2013). Plant memory: a tentative model. PubMed DOI

Trewavas A. (2003). Aspects of plant intelligence. PubMed DOI PMC

Trewavas A. (2004). Aspects of plant intelligence: an answer to Firn. PubMed DOI PMC

Trewavas A. (2005). Plant intelligence. PubMed DOI

Trewavas A. (2014).

Verhoeven K. J. F., Jansen J. J., van Dijk P. J., Biere A. (2010). Stress-induced DNA methylation changes and their heritability in asexual dandelions. PubMed DOI

Verhoeven K. J. F., Preite V. (2014). Epigenetic variation in asexually reproducing organisms. PubMed DOI

Waters E. M., Watson M. A. (2015). Live substrate positively affects root growth and stolon direction in the woodland strawberry, PubMed DOI PMC

Whittle C. A., Otto S. P., Johnston M. O., Krochko J. E. (2009). Adaptive epigenetic memory of ancestral temperature regime in DOI

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