Abstract:The mechanisms of biological evolution have always been, and still are, the subject of intense debate and modeling. One of the main problems is how the genetic variability is produced and maintained in order to make the organisms adaptable to environmental changes and therefore capable of evolving. In recent years, it has been reported that, in flies and plants, mutations in Hsp90 gene are capable to induce, with a low frequency, many different developmental abnormalities depending on the genetic backgrounds. … Show more
“…Barbara McClintock [1984] formerly suggested that the activity of mobile elements in the genome represented a reaction to environmental stressors. This hypothesis was supported by several other authors [Capy et al, 2000;Kidwell, 2002;Chénais et al, 2012;Piacentini et al, 2014], and numerous cases of transposon activation due to environmental stress conditions have been observed in plants, where one of the most influential environmental factors is represented by temperature [Vitte and Panaud, 2005;Kelly and Leitch, 2011;Chénais et al, 2012;Ito, 2013;Wheeler, 2013;Ishiguru et al, 2014;Kim et al, 2014]. Examples of correlations between environmental stressors and transposon activity are rarer in the animal kingdom.…”
Section: Mechanisms and Causessupporting
confidence: 62%
“…Examples of correlations between environmental stressors and transposon activity are rarer in the animal kingdom. However, similar connections were noted in Drosophila melanogaster , where differences in the rate of transposition were related to the development of temperature [Capy et al, 2000;Kim et al, 2014;Piacentini et al, 2014] and to the development of a resistance to pesticides [Chénais et al, 2012]. In human cells a reorganization of the transcriptome after thermal shock was described, putatively involving SINE transposon sequences [Wheeler, 2013].…”
Section: Mechanisms and Causesmentioning
confidence: 86%
“…Therefore, it represents an effective adaptive response to drastic environmental changes [Piacentini et al, 2014].…”
Section: Stimulation Of Transposon Activitymentioning
The relationship between genome size and the percentage of transposons in 161 animal species evidenced that variations in genome size are linked to the amplification or the contraction of transposable elements. The activity of transposable elements could represent a response to environmental stressors. Indeed, although with different trends in protostomes and deuterostomes, comprehensive changes in genome size were recorded in concomitance with particular periods of evolutionary history or adaptations to specific environments. During evolution, genome size and the presence of transposable elements have influenced structural and functional parameters of genomes and cells. Changes of these parameters have had an impact on morphological and functional characteristics of the organism on which natural selection directly acts. Therefore, the current situation represents a balance between insertion and amplification of transposons and the mechanisms responsible for their deletion or for decreasing their activity. Among the latter, methylation and the silencing action of small RNAs likely represent the most frequent mechanisms.
“…Barbara McClintock [1984] formerly suggested that the activity of mobile elements in the genome represented a reaction to environmental stressors. This hypothesis was supported by several other authors [Capy et al, 2000;Kidwell, 2002;Chénais et al, 2012;Piacentini et al, 2014], and numerous cases of transposon activation due to environmental stress conditions have been observed in plants, where one of the most influential environmental factors is represented by temperature [Vitte and Panaud, 2005;Kelly and Leitch, 2011;Chénais et al, 2012;Ito, 2013;Wheeler, 2013;Ishiguru et al, 2014;Kim et al, 2014]. Examples of correlations between environmental stressors and transposon activity are rarer in the animal kingdom.…”
Section: Mechanisms and Causessupporting
confidence: 62%
“…Examples of correlations between environmental stressors and transposon activity are rarer in the animal kingdom. However, similar connections were noted in Drosophila melanogaster , where differences in the rate of transposition were related to the development of temperature [Capy et al, 2000;Kim et al, 2014;Piacentini et al, 2014] and to the development of a resistance to pesticides [Chénais et al, 2012]. In human cells a reorganization of the transcriptome after thermal shock was described, putatively involving SINE transposon sequences [Wheeler, 2013].…”
Section: Mechanisms and Causesmentioning
confidence: 86%
“…Therefore, it represents an effective adaptive response to drastic environmental changes [Piacentini et al, 2014].…”
Section: Stimulation Of Transposon Activitymentioning
The relationship between genome size and the percentage of transposons in 161 animal species evidenced that variations in genome size are linked to the amplification or the contraction of transposable elements. The activity of transposable elements could represent a response to environmental stressors. Indeed, although with different trends in protostomes and deuterostomes, comprehensive changes in genome size were recorded in concomitance with particular periods of evolutionary history or adaptations to specific environments. During evolution, genome size and the presence of transposable elements have influenced structural and functional parameters of genomes and cells. Changes of these parameters have had an impact on morphological and functional characteristics of the organism on which natural selection directly acts. Therefore, the current situation represents a balance between insertion and amplification of transposons and the mechanisms responsible for their deletion or for decreasing their activity. Among the latter, methylation and the silencing action of small RNAs likely represent the most frequent mechanisms.
“…Instead, careful (and laborious) work, such as that done by some (Brink 1956;Clark and Carbon 1985;Steiner and Clarke 1994;De Vanssay et al 2012) showing frequent switching, should be considered strong evidence in the place of exhaustive sequencing. We must, however, always be concerned with the possibility of efficient inducible changes masquerading as "epigenetic" cases, e.g., mating type switching in yeasts (Haber 1998), VDJ recombination (Blackwell and Alt 1989), repeat-sequence instability (Hawley and Marcus 1989), and induced mutation (McClintock 1983;Piacentini et al 2014); after all, they do bear all of the hallmarks of epigenetic changes save one: we happen to know their mechanism. For that reason, it is critical to refrain from negative claims (that is, assertions of "no difference") as implied in "genetically identical chromosomes," when chromosomes have not been sequenced.…”
Interest in the field of epigenetics has increased rapidly over the last decade, with the term becoming more identifiable in biomedical research, scientific fields outside of the molecular sciences, such as ecology and physiology, and even mainstream culture. It has become increasingly clear, however, that different investigators ascribe different definitions to the term. Some employ epigenetics to explain changes in gene expression, others use it to refer to transgenerational effects and/or inherited expression states. This disagreement on a clear definition has made communication difficult, synthesis of epigenetic research across fields nearly impossible, and has in many ways biased methodologies and interpretations. This article discusses the history behind the multitude of definitions that have been employed since the conception of epigenetics, analyzes the components of these definitions, and offers solutions for clarifying the field and mitigating the problems that have arisen due to these definitional ambiguities.
“…Some of them may lead to genetically determined phenotypic variability. One of the mech− anisms responsible for the formation of genetic variability is associated with the presence of transposable elements (TE) (Kalendar et al 2000;Piacentini et al 2014). These mobile genetic elements have a significant impact on the organiza− tion, plasticity and evolution of genomes (Frost et al 2005).…”
Antarctic pearlwort (Colobanthus quitensis) is one of the flowering plant species considered native to maritime Antarctica. Although the species was intensively analyzed towards its morphological, anatomical and physiological adaptation to local environment, its genetic variability is still poorly studied. In the presented study, a recently developed retrotransposon−based DNA marker system (inter Primer Binding Site -iPBS) was applied to assess the genetic diversity and differentiation of C. quitensis populations from King George Island (South Shetland Islands, West Antarctic). A total of 143 scoreable bands were detected using 7 iPBS primers among 122 plant specimens representing 8 populations. 55 (38.5%) bands were found polymorphic, with an average of 14.3% polymorphic frag− ments per primer. Nine of all observed fragments were represented as a private bands de− ployed unevenly among populations. Low genetic diversity (on average H e = 0.040 and I = 0.061) and moderate population differentiation (F ST = 0.164) characterize the analyzed material. Clustering based on PCoA revealed, that the populations located on the edges of the study area diverge from the central populations. The pattern of population differentia− tion corresponds well with their geographic location and the characteristics of the sampling sites. Due to the character of iPBS markers, the observed genetic variability of populations may be explained by the genome rearrangements caused by mobilization of mobile genetic elements in the response to various stress factors. Additionally, this study demonstrates the usefulness of iPBS markers for genetic diversity studies in wild species.
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