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DNA, double stranded macromolecule that carries the hereditary information of the cell [2] and found in all living cells; [3] each cell carries chromosome(s) having a distinctive DNA sequence. [4] Examples include macromolecules such as proteins and nucleic acids, biomolecular complexes such as a ribosome, and structures such as membranes, and ...
DNA methylation is a major form of epigenetic control over gene expression and one of the most highly studied topics in epigenetics. During development, the human DNA methylation profile experiences dramatic changes. In early germ line cells, the genome has very low methylation levels. These low levels generally describe active genes.
Gene structure is the organisation of specialised sequence elements within a gene.Genes contain most of the information necessary for living cells to survive and reproduce. [1] [2] In most organisms, genes are made of DNA, where the particular DNA sequence determines the function of the gene.
For example, fruit flies share 61 percent of disease-causing genes with humans, which was important when NASA studied the bugs to learn more about what space travel might do to your genes.
Examples of mobile genetic elements in the cell (left) and the ways they can be acquired (right) Transposition of target sequence into recombination site in DNA by Transposase. Replication of the transposable sequence starts to occur when transposase cuts single strands on opposite sides of the dsDNA.
For example, the RNA component of the human telomerase contains a pseudoknot that is critical for its activity. [7] The hepatitis delta virus ribozyme is a well known example of a catalytic RNA with a pseudoknot in its active site. [10] [11] Though DNA can also form pseudoknots, they are generally not present in standard physiological conditions.
The process of semiconservative replication for the site of DNA replication is a fork-like DNA structure, the replication fork, where the DNA helix is open, or unwound, exposing unpaired DNA nucleotides for recognition and base pairing for the incorporation of free nucleotides into double-stranded DNA.
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