definição e significado de Nucleobase

Base pairing in RNA. Nucleobases in blue. Hydrogen bonds in red.

Nucleobases are a group of nitrogen-based molecules that are required to form nucleotides, the basic building blocks of DNA and RNA. Nucleobases provide the molecular structure necessary for the hydrogen bonding of complementary DNA and RNA strands, and are key components in the formation of stable DNA and RNA molecules.

Nucleobases (or nucleotide bases/nitrogenous bases/aglycones) provide the nucleotide structure necessary to form base pairs. The primary nucleobases are cytosine, guanine, adenine (DNA and RNA), thymine (DNA) and uracil (RNA), abbreviated as C, G, A, T, and U, respectively. They are usually simply called bases in genetics. Because A, G, C, and T appear in the DNA, these molecules are called DNA-bases; A, G, C, and U are called RNA-bases.

Uracil replaces thymine in RNA. These two bases are identical except that uracil lacks the 5' methyl group. Adenine and guanine belong to the double-ringed class of molecules called purines (abbreviated as R). Cytosine, thymine, and uracil are all pyrimidines (abbreviated as Y).

In normal spiral DNA the bases form pairs between the two strands: A with T and C with G. Purines pair with pyrimidines mainly for dimensional reasons - only this combination fits the constant width geometry of the DNA spiral. The A-T and C-G pairings are required to match the hydrogen bonds between the amine and carbonyl groups on the complementary bases.

The compound formed when a nucleobase forms a glycosidic bond with the 1' anomeric carbon of a ribose or deoxyribose is called a nucleoside, and a nucleoside with one or more phosphate groups attached at the 5' carbon is called a nucleotide.

Apart from adenine (A), cytosine (C), guanine (G), thymine (T) and uracil (U), DNA and RNA also contain bases that have been modified after the nucleic acid chain has been formed. In DNA, the most common modified base is 5-methylcytosine (m⁵C). In RNA, there are many modified bases, including those contained in the nucleosides pseudouridine (Ψ), dihydrouridine (D), inosine (I), and 7-methylguanosine (m⁷G).^[1]^[2]

Hypoxanthine and xanthine are two of the many bases created through mutagen presence, both of them through deamination (replacement of the amine-group with a carbonyl-group). Hypoxanthine is produced from adenine, xanthine from guanine.^[3] In similar manner, deamination of cytosine results in uracil.

In August 2011, a report, based on NASA studies with meteorites found on Earth, was published suggesting nucleobases (such as adenine, guanine, xanthine, hypoxanthine, purine, 2,6-diaminopurine, and 6,8-diaminopurine) may have been formed extraterrestrially in outer space.^[4]^[5]^[6]

1 Structure
2 Novel bases
3 See also
4 References
5 External links

Structure

The "skeleton" of adenine and guanine is purine, hence the name purine-bases.
The "skeleton" of cytosine, uracil, and thymine is pyrimidine, hence pyrimidine-bases.

Primary bases

These are incorporated into the growing chain during RNA and/or DNA synthesis.

Nucleobase	Adenine	Guanine	Thymine	Cytosine	Uracil
Nucleoside	Adenosine A	Guanosine G	Thymidine T	Cytidine C	Uridine U

Modified purine bases

These are examples of modified adenosine or guanosine.

Nucleobase	Hypoxanthine	Xanthine	7-Methylguanine
Nucleoside	Inosine I	Xanthosine X	7-Methylguanosine m⁷G

Modified pyrimidine bases

These are examples of modified cytidine, thymidine or uridine.

Nucleobase	5,6-Dihydrouracil	5-Methylcytosine
Nucleoside	Dihydrouridine D	5-Methylcytidine m⁵C

Novel bases

Main article: Nucleic acid analogues

A vast number of nucleobase analogues exist. The most common applications are used as fluorescent probes, either directly or indirectly, such as aminoallyl nucleotide, which are used to label cRNA or cDNA in microarrays. Several groups are working on alternative "extra" base pairs to extend the genetic code, such as isoguanine and isocytosine or the fluorescent 2-amino-6-(2-thienyl)purine and pyrrole-2-carbaldehyde.^{[citation needed]}

In medicine, several nucleoside analogues are used as anticancer and antiviral agents. The viral polymerase incorporates these compounds with non-canon bases. These compounds are activated in the cells by being converted into nucleotides; they are administered as nucleosides as charged nucleotides cannot easily cross cell membranes.^{[citation needed]}

References

^ BIOL2060: Translation
^ "Role of 5' mRNA and 5' U snRNA cap structures in regulation of gene expression" - Research - Retrieved 13 December 2010.
^ T Nguyen, D Brunson, C L Crespi, B W Penman, J S Wishnok, and S R Tannenbaum, DNA damage and mutation in human cells exposed to nitric oxide in vitro, Proc Natl Acad Sci U S A. 1992 April 1; 89(7): 3030–3034
^ Callahan; Smith, K.E.; Cleaves, H.J.; Ruzica, J.; Stern, J.C.; Glavin, D.P.; House, C.H.; Dworkin, J.P. (11 August 2011). "Carbonaceous meteorites contain a wide range of extraterrestrial nucleobases". PNAS. DOI:10.1073/pnas.1106493108. http://www.pnas.org/content/early/2011/08/10/1106493108. Retrieved 2011-08-15.
^ Steigerwald, John (08 August 2011). "NASA Researchers: DNA Building Blocks Can Be Made in Space". NASA. http://www.nasa.gov/topics/solarsystem/features/dna-meteorites.html. Retrieved 2011-08-10.
^ ScienceDaily Staff (09 August 2011). "DNA Building Blocks Can Be Made in Space, NASA Evidence Suggests". ScienceDaily. http://www.sciencedaily.com/releases/2011/08/110808220659.htm. Retrieved 2011-08-09.

External links

Base pairing in DNA Double Helix (shows specific hydrogen bonds)

Nucleic acid constituents

Nucleobase

Purine (Adenine, Guanine, Purine analogue) · Pyrimidine (Uracil, Thymine, Cytosine, Pyrimidine analogue)

Nucleoside

Ribonucleoside	Adenosine · Guanosine · 5-Methyluridine · Uridine · Cytidine

Deoxyribonucleoside	Deoxyadenosine · Deoxyguanosine · Thymidine · Deoxyuridine · Deoxycytidine