AI Article Synopsis

  • Long-term cultivation of cell lines affects the synthesis of biologically active substances in traditional medicine, with a focus on the rDNA cluster variations in Oriental ginseng.
  • Analysis of cell lines cultivated for 6 and 24 years revealed mutations in 18S rDNA sequences, correlating with increased nucleoli and chromosome numbers.
  • The study indicates that these changes are linked to somaclonal variation and may alter gene expression regulation through heterogeneous ribosomes, highlighting the importance of specific culture conditions on genetic stability.

Article Abstract

Long-term cultivation of cell lines leads to a decreasing synthesis of the biologically active substances used in traditional medicine. To gain insight into the cellular mechanisms which may influence this process, we analyzed variations within the rDNA cluster of the Oriental ginseng cell lines. The cell lines were cultivated for 6 and 24 years; the number of nucleoli and chromosomes was analyzed. The complete 18S rDNA sequences were cloned and sequenced. The nucleotide polymorphism and phylogenetic relations of the sequences were analyzed, and the secondary structures for separate 18S rRNA regions were modeled. The 18S rDNA accumulated mutations during cell cultivation that correlate well with an increase in the number of chromosomes and nucleoli. The patterns of nucleotide diversity are culture-specific and the increasing polymorphism associates with cytosine methylation sites. The secondary structures of some 18S rRNA regions and their interaction can alter during cultivation. The phylogenetic tree topologies are particular for each cell line.The observed alterations in rDNA clusters are associated with a somaclonal variation, leading to changes in the pattern of intracellular synthesis during cell cultivation. The identified divergent rRNAs could provide additional gene expression regulation in cells by forming heterogeneous ribosomes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7599642PMC
http://dx.doi.org/10.3390/biom10101410DOI Listing

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