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Mitochondrial DNA is a main source of this extrachromosomal DNA in eukaryotes. [5] The fact that this organelle contains its own DNA supports the hypothesis that mitochondria originated as bacterial cells engulfed by ancestral eukaryotic cells. [6] Extrachromosomal DNA is often used in research into replication because it is easy to identify ...
Extrachromosomal circular DNA (eccDNA) is a type of double-stranded circular DNA structure that was first discovered in 1964 by Alix Bassel and Yasuo Hotta. [1] In contrast to previously identified circular DNA structures (e.g., bacterial plasmids, mitochondrial DNA, circular bacterial chromosomes, or chloroplast DNA), eccDNA are circular DNA found in the eukaryotic nuclei of plant and animal ...
A plasmid is a small, extrachromosomal DNA molecule within a cell that is physically separated from chromosomal DNA and can replicate independently. They are most commonly found as small circular, double-stranded DNA molecules in bacteria; however, plasmids are sometimes present in archaea and eukaryotic organisms.
CpG-islands characteristic in microDNA compared to a single C-G bp. [1] MicroDNA is the most abundant subtype of Extrachromosomal Circular DNA (eccDNA) in humans, typically ranging from 200-400 base pairs in length and enriched in non-repetitive genomic sequences with a high density of exons.
DNA transposons, LTR retrotransposons, SINEs, and LINEs make up a majority of the human genome. Mobile genetic elements (MGEs), sometimes called selfish genetic elements, [1] are a type of genetic material that can move around within a genome, or that can be transferred from one species or replicon to another. MGEs are found in all organisms.
Circular extrachromosomal DNA are not only found in yeast but other eukaryotic organisms. [15] [16] A regulated formation of eccDNA in preblastua Xenopus embryos has been developed. The population of circular rDNA is decreased in embryos, indicative of the circular rDNA migrating to linear DNA, as was shown in their analysis on 2D gel ...
An extrachromosomal array is a method for mosaic analysis in genetics. It is a cosmid, and contains two functioning closely linked genes: a gene of interest and a mosaic marker. Such an array is injected into germ line cells, which already contain mutant (specifically, loss of function) alleles of all three genes in their chromosomal DNA.
With the onset of these discoveries, several approaches in classifying different components of multipartite genomes were proposed. Various terms have been used to describe large replicons other than the main chromosome, including simply designating them as additional chromosomes, or "minichromosomes", "megaplasmids", or "secondary chromosomes".