Epigenetic Memory as a Basis for Intelligent Behavior in Clonal Plants
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
27630664
PubMed Central
PMC5006084
DOI
10.3389/fpls.2016.01354
Knihovny.cz E-zdroje
- Klíčová slova
- 5-azacytidine, DNA methylation, asexual reproduction, between ramets communication, plant memory, zebularine,
- Publikační typ
- časopisecké články MeSH
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.
Ecological Research Institute Kingston NY USA
Institute of Botany of Czech Academy of Sciences Průhonice Czech Republic
Zobrazit více v PubMed
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
The evolutionary consequences of interactions between the epigenome, the genome and the environment
Exploring the crop epigenome: a comparison of DNA methylation profiling techniques
Deciphering the Epigenetic Alphabet Involved in Transgenerational Stress Memory in Crops
Anticipatory Behavior of the Clonal Plant Fragaria vesca
Transgenerational Effects and Epigenetic Memory in the Clonal Plant Trifolium repens