2022
DOI: 10.1007/s12892-022-00172-2
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Evaluation of ethyl methanesulfonate-induced in vitro mutagenesis, polymorphism and genomic instability in wheat (Triticum aestivum L.)

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Cited by 8 publications
(6 citation statements)
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“…The study by Temel et al [ 50 ] propounds that DNA methylation is optimally elucidated within tissue culture research through the prism of the CRED methodology. The amalgamation of iPBS and CRED methodologies [ 14 , 15 , 16 , 17 , 18 ] constitutes a boon for tissue culture investigations, empowering the delineation of both genetic and epigenetic transformations. In the current research, the synergy of iPBS and CRED was harnessed to unravel the polyamine-induced perturbations in the genetic and epigenetic landscapes of wheat.…”
Section: Discussionmentioning
confidence: 99%
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“…The study by Temel et al [ 50 ] propounds that DNA methylation is optimally elucidated within tissue culture research through the prism of the CRED methodology. The amalgamation of iPBS and CRED methodologies [ 14 , 15 , 16 , 17 , 18 ] constitutes a boon for tissue culture investigations, empowering the delineation of both genetic and epigenetic transformations. In the current research, the synergy of iPBS and CRED was harnessed to unravel the polyamine-induced perturbations in the genetic and epigenetic landscapes of wheat.…”
Section: Discussionmentioning
confidence: 99%
“…In the realm of plant biology, the spectrum of epigenetic variations encompasses diverse phenomena, such as point mutations, deletions, transposable element activations, rearrangements, and changes in ploidy [ 9 , 10 ], as well as alterations to the DNA structure itself [ 11 ]. Various molecular markers, including single nucleotide polymorphisms (SNPs), microsatellites (SSRs), simple sequence repeat polymorphisms (ISSRs), fragment length polymorphisms (RFLPs), and random amplified polymorphic DNA (RAPD) markers [ 12 ], alongside the inter-primer binding site (iPBS) retrotransposon [ 13 , 14 ], are currently harnessed for detecting polymorphic states and DNA methylation patterns [ 15 , 16 , 17 , 18 ]. Within the context of epigenetic modulation, DNA methylation emerges as a pivotal process, universally governing gene expression and the repression of transposable elements.…”
Section: Introductionmentioning
confidence: 99%
“…When compared to the control, the RAPD profiles revealed polymorphism when a band that was predicted to be present did not exist and a novel band did appear. Changes in the average polymorphism were calculated for each treatment group (changing concentrations of AgNO 3 and Ag-NPs), and the results were reported as a percentage in comparison to the value obtained from the control (which was set to 100%) [ 45 , 46 , 104 , 105 ]. A quantitative metric known as genomic template stability (GTS%) was estimated for RAPD using the formula GTS = (1 − a/n) × 100.…”
Section: Methodsmentioning
confidence: 99%
“…In this calculation, a represents the mean number of polymorphic bands in each treated template, and n represents the total number of bands in the control [ 38 , 103 ]. With the use of the formula Polymorphism = a/n × 100 [ 45 , 46 , 104 , 105 ], we were able to calculate the average polymorphism values (in percent) for each concentration.…”
Section: Methodsmentioning
confidence: 99%
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