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The expression of genes encoded in DNA begins by transcribing the gene into RNA, a second type of nucleic acid that is very similar to DNA, but whose monomers contain the sugar ribose rather than deoxyribose. RNA also contains the base uracil in place of thymine. RNA molecules are less stable than DNA and are typically single-stranded.
The genetic code is the set of rules used by living cells to translate information encoded within genetic material (DNA or RNA sequences of nucleotide triplets or codons) into proteins. Translation is accomplished by the ribosome , which links proteinogenic amino acids in an order specified by messenger RNA (mRNA), using transfer RNA (tRNA ...
Knowing the sequence of the protein encoded by a gene can allow researchers to apply methods that find similarities among protein sequences that provide more information than similarities or differences among DNA sequences. If the genes of a gene family encode proteins, the term protein family is often used in an analogous manner to gene family.
Gene duplication is a major mechanism through which new genetic material is generated during molecular evolution. For example, the olfactory receptor gene family is one of the best-documented examples of pseudogenes in the human genome. More than 60 percent of the genes in this family are non-functional pseudogenes in humans.
For example, leuA is one of the genes of the leucine biosynthetic pathway, and leuA273 is a particular allele of this gene. Where the actual protein coded by the gene is known then it may become part of the basis of the mnemonic, thus: rpoA encodes the α-subunit of RNA polymerase; rpoB encodes the β-subunit of RNA polymerase; polA encodes DNA ...
Repetitive regions may produce performance issues if they are not masked, and may even produce false evidence for gene annotation (for example, treating an open reading frame (ORF) in a transposon as an exon) [24] Depending on the letters used for replacement, masking can be classified as soft or hard: in soft masking, repetitive regions are ...
These statistics are interesting, even if they represent a substantial oversimplification of what is really going on. Here is an example. Suppose there are 10,000 genes in an experiment, only 50 (0.5%) of which play a known role in making cholesterol. The experiment identifies 200 regulated genes.
Non-functional DNA elements such as pseudogenes and repetitive DNA, both of which are types of junk DNA, can also be found in intergenic regions—although they may also be located within genes in introns. [2] It is possible that these regions contain as of yet unidentified functional elements, such as non-coding genes or regulatory sequences. [3]