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Cladogram showing the relationships between Ty1-copia and Ty3-gypsy retrotransposable element superfamilies identified in the transcriptome of B. decumbens within contigs/unigenes (black names) or as characteristic domains (red). Arrows indicate the gypsy LTR-RTs sequences used to design primers for in situ hybridization (Table 1)

Cladogram showing the relationships between Ty1-copia and Ty3-gypsy retrotransposable element superfamilies identified in the transcriptome of B. decumbens within contigs/unigenes (black names) or as characteristic domains (red). Arrows indicate the gypsy LTR-RTs sequences used to design primers for in situ hybridization (Table 1)

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Like other eukaryotes, the nuclear genome of plants consists of DNA with a small proportion of low- copy DNA (genes and regulatory sequences) and very abundant DNA sequence motifs that are repeated thou- sands up to millions of times in the genomes including transposable elements (TEs) and satellite DNA. Retrotransposons, one class of TEs, are sequ...

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... Additionally, differences in the ratio between Gypsy and Copia have been observed in different groups. Gypsy was the most abundant retrotransposon in Helianthus and Brachiaria [37,38], whereas Copia was the most abundant in Rhynchospora [39]. ...
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... In this study, we used both specific probes developed using graph-based sequence clustering compared with "universal" conserved regions of Ty1-copia and Ty3-gypsy retroelements. Similar to Urochloa tropical forage grasses, where genomic DNA and retroelements used as probes showed no substantial differences between the genomes (Santos et al., 2015;Tomaszewska et al., 2021b), parallel universal retroelement repeats used in this study were relatively equally abundant over the whole Cenchrus ciliaris genome (see Supplementary Figure 1). The Gy105 probe (see Figure 1D) labeled some chromosomes as more weaker. ...
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Cenchrus ciliaris is an apomictic, allotetraploid pasture grass widely distributed in the tropical and subtropical regions of Africa and Asia. In this study, we aimed to investigate the genomic organization and characterize some of the repetitive DNA sequences in this species. Due to the apomictic propagation, various aneuploid genotypes are found, and here, we analyzed a 2n = 4x + 3 = 39 accession. The physical mapping of Ty1-copia and Ty3-gypsy retroelements through fluorescence in situ hybridization with a global assessment of 5-methylcytosine DNA methylation through immunostaining revealed the genome-wide distribution pattern of retroelements and their association with DNA methylation. Approximately one-third of Ty1-copia sites overlapped or spanned centromeric DAPI-positive heterochromatin, while the centromeric regions and arms of some chromosomes were labeled with Ty3-gypsy. Most of the retroelement sites overlapped with 5-methylcytosine signals, except for some Ty3-gypsy on the arms of chromosomes, which did not overlap with anti-5-mC signals. Universal retrotransposon probes did not distinguish genomes of C. ciliaris showing signals in pericentromeric regions of all 39 chromosomes, unlike highly abundant repetitive DNA motifs found in survey genome sequences of C. ciliaris using graph-based clustering. The probes developed from RepeatExplorer clusters gave strong in situ hybridization signals, mostly in pericentromeric regions of about half of the chromosomes, and we suggested that they differentiate the two ancestral genomes in the allotetraploid C. ciliaris, likely having different repeat sequence variants amplified before the genomes came together in the tetraploid.
... The karyotype organization that has been observed suggests an allopolyploid origin for U. brizantha, corroborating the results from a study of the physical mapping of rDNA genes in this species (Nielen et al., 2009). In another study, the occurrence, mapping, and distribution of gypsy retrotransposons in U. decumbens, U. brizantha, U. ruziziensis and U. humidicola showed that mobile elements, in addition to the chromosome number variation, contributed to karyotype evolution (Santos et al., 2015b;Worthington et al., 2021). ...
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... The karyotype organization that has been observed suggests an allopolyploid origin for U. brizantha, corroborating the results from a study of the physical mapping of rDNA genes in this species (Nielen et al., 2009). In another study, the occurrence, mapping, and distribution of gypsy retrotransposons in U. decumbens, U. brizantha, U. ruziziensis and U. humidicola showed that mobile elements, in addition to the chromosome number variation, contributed to karyotype evolution (Santos et al., 2015b;Worthington et al., 2021). ...
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Background LTR retrotransposons play a significant role in plant growth, genome evolution, and environmental stress response, but their regulatory response to heat stress remains unclear. We have investigated the activities of two LTR retrotransposons, PHRE1 and PHRE2, of moso bamboo (Phyllostachys edulis) in response to heat stress. Results The differential overexpression of PHRE1 and PHRE2 with or without CaMV35s promoter showed enhanced expression under heat stress in transgenic plants. The transcriptional activity studies showed an increase in transposition activity and copy number among moso bamboo wild type and Arabidopsis transgenic plants under heat stress. Comparison of promoter activity in transgenic plants indicated that 5’LTR promoter activity was higher than CaMV35s promoter. Additionally, yeast one-hybrid (Y1H) system and in planta biomolecular fluorescence complementation (BiFC) assay revealed interactions of heat-dependent transcription factors (TFs) with 5’LTR sequence and direct interactions of TFs with pol and gag. Conclusions Our results conclude that the 5’LTR acts as a promoter and could regulate the LTR retrotransposons in moso bamboo under heat stress.
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... Physical mapping of 5S and 18S-5.8S-25S rDNA locations provides a chromosome marker, but the mostly similar patterns in the 'brizantha' complex did not assist in identification of genome composition (see Fig. 2; Akiyama et al., 2010;Nielen et al., 2010;Santos et al., 2015;Nani et al., 2018). In the three accessions with desirable agronomic characteristics that could not be assigned to species based on morphology, the number of rDNA sites did not correspond to ploidy, with only one pair of 45S rDNA sites in the two tetraploids (two pairs of sites expected), and four 45S sites in a pentaploid (expectation five), suggesting a more complex origin involving processes such as karyotype reorganization, aneuploidy or segmental allopolyploidy and introgression. ...
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... Previous studies reported variation in the richness and predominant lineages of TEs within the Poaceae family (Křivánková et al., 2017). Other grasses, such as Brachiaria decumbens Stapf, present a genome Ty3-Gypsy profile similar to that of D. antarctica (Santos et al., 2015). However, in other cases, as in the F. pratensis genome, the most abundant retroelement observed belongs to the Athila family (Křivánková et al., 2017). ...
... The results obtained for Ty3-Gypsy families, Tekay and TatV, showed their distribution throughout all the chromosomes in both localities, presenting an increase of hybridization signals in the proximal and centromeric regions. This observation agrees with the general distribution of retrotransposon sequences of the order LTR belonging to the Ty3-Gypsy superfamily in most grasses, such as Brachiaria (Santos et al., 2015), Triticeae (Belyayev et al., 2005), F. pratensis (Křivánková et al., 2017), Oryza, and Z. mays (Li et al., 2017) and in other groups, such as Arabidopsis thaliana (L.) Heynh. (Li et al., 2017). ...
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... Several studies (reviewed in Vicient and Casacuberta, 2017) have reported transcriptional reactivation of some TE lineages in hybrids and allopolyploids or new insertions as found in tobacco, sunflower, wheat, or Brachiaria sp. (Ungerer et al., 2006;Petit et al., 2010;Yaakov and Kashkush, 2012;Santos et al., 2015). As TE expression is controlled by epigenetic regulation (e.g., DNA hypermethylation and siRNAs), new TE regulation following polyploid speciation may result in altered neighbor gene expression including gene silencing and novel gene expression patterns (Kashkush et al., 2003;Hollister and Gaut, 2009;Parisod et al., 2010a;Zhang et al., 2015;Lerat et al., 2019). ...
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... possesses various polyploid species with different basic chromosome number (× = 6 to × = 9). The occurence, mapping and distribution of gypsy retrotransposons in the karyotype of Brachiaria decumbens (Mez) Davidse, B. brizantha (Mez) Davidse, B. ruziziensis (Mez) Davidse and B. humidicola (Mez) Davidse evidenced that, besides the chromosome number variation, mobile elements also contributed to karyotype evolution [68]. In addition, genetic variation was showed in polyploid Paspalum species from SSR markers developed for this genus. ...
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Polyploidy means having more than two basic sets of chromosomes. Polyploid plants may be artificially obtained through chemical, physical and biological (2n gametes) methods. This approach allows an increased gene scope and expression, thus resulting in phenotypic changes such as yield and product quality. Nonetheless, breeding new cultivars through induced polyploidy should overcome deleterious effects that are partly contributed by genome and epigenome instability after polyploidization. Furthermore, shortening the time required from early chromosome set doubling to the final selection of high yielding superior polyploids is a must. Despite these hurdles, plant breeders have successfully obtained polyploid bred-germplasm in broad range of forages after optimizing methods, concentration and time, particularly when using colchicine. These experimental polyploids are a valuable tool for understanding gene expression, which seems to be driven by dosage dependent gene expression, altered gene regulation and epigenetic changes. Isozymes and DNA-based markers facilitated the identification of rare alleles for particular loci when compared with diploids, and also explained their heterozygosity, phenotypic plasticity and adaptability to diverse environments. Experimentally induced polyploid germplasm could enhance fresh herb-age yield and quality, e.g., leaf protein content, leaf total soluble solids, water soluble carbohydrates and sucrose content. Offspring of experimentally obtained hybrids should undergo selection for several generations to improve their performance and stability.
... The occurence, mapping and distribution of gypsy retrotransposons in the karyotype of Brachiaria decumbens, B. brizantha, B. ruziziensis and B. humidicola evidenced that, besides the chromosome number variation, mobile elements also contributed to karyotype evolution [56]. In addition, genetic variation was showed in polyploid Paspalum species from SSR markers developed for this genus. ...
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Full-text available
Polyploidy means having more than two basic sets of chromosomes. Polyploid plants may be artificially obtained through chemical, physical and biological (2n gametes) methods. This approach allows an increased gene scope and expression, thus resulting in phenotypic changes such as yield and product quality. Nonetheless, breeding new cultivars through induced polyploidy should overcome deleterious effects that are partly contributed by genome and epigenome instability after polyploidization. Furthermore, shortening the time required from early chromosome set doubling to the final selection of high yielding superior polyploids is a must. Despite these hurdles, plant breeders have successfully obtained polyploid bred-germplasm in broad range of forages after optimizing methods, concentration and time, particularly when using colchicine. These experimental polyploids are a valuable tool for understanding gene expression, which seems to be driven by dosage dependent gene expression, altered gene regulation and epigenetic changes. Isozymes and DNA-based markers facilitated the identification of rare alleles for particular loci when compared with diploids, and also explained their heterozygosity, phenotypic plasticity and adaptability to diverse environments. Experimentally induced polyploid germplasm could enhance fresh herbage yield and quality, e.g. leaf protein content, leaf total soluble solids, water soluble carbohydrates and sucrose content. Offspring of experimentally obtained hybrids should undergo selection for several generations to improve their performance and stability.