Nucleic acids
A
nucleic acid
is a macromolecule composed of chains of monomeric nucleotides. In biochemistry thesemolecules carry genetic information or form structures within cells. The most common nucleic acids are
deoxyribonucleic acid
(DNA) and
ribonucleic acid
(RNA). Nucleic acids are universal in living things, as theyare found in all cells and viruses. Nucleic acids were first discovered by Friedrich Miescher.Artificial nucleic acids include
peptide nucleic acid
(PNA),
Morpholino
and
locked nucleic acid
(LNA),as well as
glycol nucleic acid
(GNA) and
threose nucleic acid
(TNA). Each of these is distinguished fromnaturally-occurring DNA or RNA by changes to the backbone of the moleculeThe term "nucleic acid" is the generic name for a family of biopolymers, named for their role in the cellnucleus. The monomers from which nucleic acids are constructed are called nucleotides.Each nucleotide consists of three components: a nitrogenous heterocyclicbase, which is either a purine or a pyrimidine; a pentosesugar; and a phosphate group. Nucleic acid types differ in the structure of the sugar in their nucleotides - DNA contains 2-deoxyriboses while RNA contains ribose (where the only difference is the presenceof a hydroxyl group). Also, the nitrogenous bases found in the two nucleic acid types are different: adenine,cytosine, and guanine are found in both RNA and DNA, while thymine only occurs in DNA and uracil only occursin RNA. Other rare nucleic acid bases can occur, for example inosine in strands of mature transfer RNA. Nucleic acids are usually either single-stranded or double-stranded, though structures with three or morestrands can form. A double-stranded nucleic acid consists of two single-stranded nucleic acids held together byhydrogen bonds, such as in the DNA double helix. In contrast, RNA is usually single-stranded, but any givenstrand may fold back upon itself to form secondary structure as in tRNA and rRNA. Within cells, DNA is usuallydouble-stranded, though some viruses have single-stranded DNA as their genome. Retroviruses have single-stranded RNA as their genome.The sugars and phosphates in nucleic acids are connected to each other in an alternating chain, linked byshared oxygens, forming a phosphodiester bond. In conventional nomenclature, the carbons to which the phosphategroups attach are the 3' end and the 5' end carbons of the sugar. This gives nucleic acids polarity. The bases extendfrom a glycosidic linkage to the 1' carbon of the pentose sugar ring. Bases are joined through N-1 of pyrimidinesand N-9 of purines to 1' carbon of ribose through N-
β glycosyl bond.
Nucleosides
are glycosylamines consisting of a nucleobase (often referred to simply
base
) bound to aribose or deoxyribosesugar. Examples of these include cytidine, uridine, adenosine, guanosine, thymidine andinosine. Nucleosides can be phosphorylated by specific kinases in the cell on the sugar's primary alcohol group (-CH
2
−
OH), producing nucleotides, which are the molecular building blocks of DNA and RNA. Nucleosides can be produced by de novo synthesis pathways, particularly in the liver; but they are more abundantlysupplied via ingestion and digestion of nucleic acids in the diet, whereby nucleotidases break down
nucleotides
(such as the thymine nucleotide) into
nucleosides
(such as thymidine) and phosphate. The nucleosides, in turn, aresubsequently broken down:
in the lumen of the digestive system by nucleosidases into nucleobases and ribose deoxyribose)
inside the cell by nucleoside phosphorylases into nitrogenous bases, and ribose-1-phosphate or deoxyribose-1-phosphate.In medicine several nucleoside analogues are used as antiviral or anticancer agents. The viral polymeraseincorporates these compounds with non-canon bases. These compounds are activated in the cells by beingconverted into nucleotides, they are administered as nuclosides since charged nucleotides cannot easily cross cellmembranes.
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