Methylation Sensitive Amplification Polymorphism (MSAP) is a method for assessing DNA methylation changes in organisms. After restriction digestion, the method involves electrophoresis based visualization of PCR fragments from selectively amplified DNA and analysis of differences between sample specific methylation profiles. The method can be used for quality assurance of in vitro cultures where changes also need to be monitored at the epigenetic level and not only at the genetic level. In this master’s thesis, we present our approach to perform MSAP analyzes on in vivo and in vitro cultures of C. sativa L. We compared methylation profiles of C. sativa samples with the aim of evaluating their epigenetic stability during in vivo clonal propagation from stem cuttings and during successive in vitro subcultures based on shoot organogenesis from nodal explants. When analyzing the in vivo plants, we observed significant differences between methylation profiles of C. sativa clones. Regarding in vitro analysis there was an expected significant difference between methylation profiles of donor plants grown in vivo and subsequent in vitro cultures, due to different environmental conditions and plant developmental stages, while we did not detect significant differences in methylation profiles between plantlets from the 1st and the 5th subculture. These results indicate that C. sativa maintains its epigenetic integrity throughout micropropagation cycles.
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