Abstract:The importance of tree genetic variability in the ability of forests to respond and adapt to environmental changes is crucial in forest management and conservation. Along with genetics, recent advances have highlighted “epigenetics” as an emerging and promising field of research for the understanding of tree phenotypic plasticity and adaptive responses. In this paper, we review recent advances in this emerging field and their potential applications for tree researchers and breeders, as well as for forest manag… Show more
“…During the annual cycle, for example, different developmental transitions like bud set in autumn and bud burst in spring are governed by changes in DNA methylation patterns [ 29 ]. Moreover, these epigenetic alterations and the establishment of epigenetic marks strongly contribute to the development of phenotypic plasticity and environmental stress memory through the differential expression of specific genes and the regulation of transposable elements mobility [ 5 ]. Despite this fact, only limited studies have been implemented with trees and we still lack information about the multiple regulatory layers connecting epigenetic variations, gene expression, and phenotypic traits in trees.…”
Section: Discussionmentioning
confidence: 99%
“…DNA methylation is the most studied epigenetic mark due to its occurrence in plants and mammals, its stability, and its role in gene regulation and genome structure maintenance through transposon silencing [ 5 ]. Methylation is site specific and usually occurs in the fifth carbon position of cytosines in the following sequences: CG, CHG, and CHH (where H = A, T or C) [ 6 ].…”
Based on the hypothesis that embryo development is a crucial stage for the formation of stable epigenetic marks that could modulate the behaviour of the resulting plants, in this study, radiata pine somatic embryogenesis was induced at high temperatures (23 °C, eight weeks, control; 40 °C, 4 h; 60 °C, 5 min) and the global methylation and hydroxymethylation levels of emerging embryonal masses and somatic plants were analysed using LC-ESI-MS/ MS-MRM. In this context, the expression pattern of six genes previously described as stress-mediators was studied throughout the embryogenic process until plant level to assess whether the observed epigenetic changes could have provoked a sustained alteration of the transcriptome. Results indicated that the highest temperatures led to hypomethylation of both embryonal masses and somatic plants. Moreover, we detected for the first time in a pine species the presence of 5-hydroxymethylcytosine, and revealed its tissue specificity and potential involvement in heat-stress responses. Additionally, a heat shock protein-coding gene showed a down-regulation tendency along the process, with a special emphasis given to embryonal masses at first subculture and ex vitro somatic plants. Likewise, the transcripts of several proteins related with translation, oxidative stress response, and drought resilience were differentially expressed.
“…During the annual cycle, for example, different developmental transitions like bud set in autumn and bud burst in spring are governed by changes in DNA methylation patterns [ 29 ]. Moreover, these epigenetic alterations and the establishment of epigenetic marks strongly contribute to the development of phenotypic plasticity and environmental stress memory through the differential expression of specific genes and the regulation of transposable elements mobility [ 5 ]. Despite this fact, only limited studies have been implemented with trees and we still lack information about the multiple regulatory layers connecting epigenetic variations, gene expression, and phenotypic traits in trees.…”
Section: Discussionmentioning
confidence: 99%
“…DNA methylation is the most studied epigenetic mark due to its occurrence in plants and mammals, its stability, and its role in gene regulation and genome structure maintenance through transposon silencing [ 5 ]. Methylation is site specific and usually occurs in the fifth carbon position of cytosines in the following sequences: CG, CHG, and CHH (where H = A, T or C) [ 6 ].…”
Based on the hypothesis that embryo development is a crucial stage for the formation of stable epigenetic marks that could modulate the behaviour of the resulting plants, in this study, radiata pine somatic embryogenesis was induced at high temperatures (23 °C, eight weeks, control; 40 °C, 4 h; 60 °C, 5 min) and the global methylation and hydroxymethylation levels of emerging embryonal masses and somatic plants were analysed using LC-ESI-MS/ MS-MRM. In this context, the expression pattern of six genes previously described as stress-mediators was studied throughout the embryogenic process until plant level to assess whether the observed epigenetic changes could have provoked a sustained alteration of the transcriptome. Results indicated that the highest temperatures led to hypomethylation of both embryonal masses and somatic plants. Moreover, we detected for the first time in a pine species the presence of 5-hydroxymethylcytosine, and revealed its tissue specificity and potential involvement in heat-stress responses. Additionally, a heat shock protein-coding gene showed a down-regulation tendency along the process, with a special emphasis given to embryonal masses at first subculture and ex vitro somatic plants. Likewise, the transcripts of several proteins related with translation, oxidative stress response, and drought resilience were differentially expressed.
“…For trans-generational memory the repetition of the stress in successive generations is key for keeping the transcriptional state associated with the primed response [ 46 , 190 , 191 ] and a stress recovery phase of the mother plants may be crucial [ 191 ]. Although priming has been well-studied in annual plants, such as Arabidopsis [ 179 ] or the model crops maize and rice [ 172 , 192 , 193 ], the molecular memory induced by stress may indeed be particularly relevant for perennial species, among them economically important crops such as poplar [ 65 , 66 , 194 ], and clonally propagated plants, for instance grapevine [ 195 ]. In addition, maintaining the primed state required to surpass the energetic costs, otherwise resetting the memory, may be more advantageous for the plant [ 181 , 187 , 191 ].…”
Section: Epigenetic Advances In Crop Improvement: Exploiting Epigenetic Diversitymentioning
confidence: 99%
“…The authors proposed (i) “concurrent analysis of epigenetic variation and phenotypic trait variation, including plant fitness between individuals exposed to contrasted biotic interactions” and (ii) “analysis of specific loci and physiological pathways to clarify the epigenetic contribution to the stabilisation of environmentally induced phenotypes (priming) or across generations’’ to gain insights into functional relationships. In addition to these recommendations, Amaral [ 194 ] proposed a complementary methodological plan for tree breeding that can be easily extended to crops, including (i) use of both forward and reverse (epi)genetic approaches and development of population epigenomics; (ii) assessment of the effects of multiple, potentially interacting, stressful conditions (intensity, duration, frequency, interaction); (iii) favour of field experimental designs; (iv) use of kinetics approaches by sampling biological material along a developmental gradient for a better understanding of the molecular chain acting from short to long term during development and environment interactions; (v) taking into account crop features (species, genotype or variety, physiological and chronological ages, organs, tissues), but also the geographic origin, clone or seed history, clonal propagation vs. sexual reproduction, and all features of breeding, management of genetic resources and culture; and (vi) development of trans-omics approach to overcome the lack of comprehensive understanding and the information gap regarding interaction across multiple -omic layers to move from correlative to causal inference and predictions.…”
Section: Gaps In Knowledge and Future Challengesmentioning
confidence: 99%
“…Increasing evidence indicates that together with hormones, epigenetic mechanisms play an important role in somatic embryogenesis induction and progression [ 275 , 279 , 280 ]. This data opens the door for targeting epigenetics as a potential biotech strategy to improve and accelerate crop plant regeneration and breeding [ 66 , 194 ]. For these studies, methodologies to monitor changes in global DNA methylation levels and nuclear patterns have been very useful [ 281 , 282 ].…”
Section: Gaps In Knowledge and Future Challengesmentioning
Epigenetics has emerged as an important research field for crop improvement under the on-going climatic changes. Heritable epigenetic changes can arise independently of DNA sequence alterations and have been associated with altered gene expression and transmitted phenotypic variation. By modulating plant development and physiological responses to environmental conditions, epigenetic diversity—naturally, genetically, chemically, or environmentally induced—can help optimise crop traits in an era challenged by global climate change. Beyond DNA sequence variation, the epigenetic modifications may contribute to breeding by providing useful markers and allowing the use of epigenome diversity to predict plant performance and increase final crop production. Given the difficulties in transferring the knowledge of the epigenetic mechanisms from model plants to crops, various strategies have emerged. Among those strategies are modelling frameworks dedicated to predicting epigenetically controlled-adaptive traits, the use of epigenetics for in vitro regeneration to accelerate crop breeding, and changes of specific epigenetic marks that modulate gene expression of traits of interest. The key challenge that agriculture faces in the 21st century is to increase crop production by speeding up the breeding of resilient crop species. Therefore, epigenetics provides fundamental molecular information with potential direct applications in crop enhancement, tolerance, and adaptation within the context of climate change.
An increase in the frequency and magnitude of drought events threatens the health of forests and the economic, ecological, and societal services they provide. It has been widely demonstrated that trees undergoing a succession of stresses may accumulate lesions that in turn lead to a decrease in their vigor and eventually to death. However, recent studies have shown that a nonlethal stress should also initiate a stress memory, which triggers a faster and stronger plant defensive response when a new stress occurs. Although this mechanism is well understood in many herbaceous plants, a better understanding in trees is needed. The aim of our study was to explore the capacity of two forest tree species to develop a stress memory. A greenhouse experiment was conducted to evaluate the tree seedlings' vigor after one or two consecutive droughts separate from a rehydration period during the same growing season. No stress memory pattern was observed for the two tree species as, on the contrary, we even observed a stress accumulation pattern in sugar maple. It remains possible that some individuals in our study developed stress memory, but that we were not able to detect it. The fine‐tuning of experimental parameters and the conducting of longitudinal studies would be helpful to detect individual capacity in stress memory activation.
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