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Thymine () (symbol T or Thy) is one of the four in the of that are represented by the letters G–C–A–T. The others are , , and . Thymine is also known as 5-methyluracil, a nucleobase. In , thymine is replaced by the nucleobase . Thymine was first isolated in 1893 by and Albert Neumann from calf glands, hence its name.


Derivation
As its alternate name (5-methyluracil) suggests, thymine may be derived by of uracil at the 5th carbon. In , thymine is replaced with in most cases. In DNA, thymine (T) binds to (A) via two hydrogen bonds, thereby stabilizing the nucleic acid structures.

Thymine combined with creates the , which is synonymous with the term . Thymidine can be phosphorylated with up to three phosphoric acid groups, producing ( deoxy thymidine mono phosphate), , or (for the di- and tri- phosphates, respectively).

One of the common mutations of DNA involves two adjacent thymines or cytosine, which, in presence of , may form , causing "kinks" in the DNA molecule that inhibit normal function.

Thymine could also be a target for actions of 5- (5-FU) in treatment. 5-FU can be a metabolic analog of thymine (in DNA synthesis) or uracil (in RNA synthesis). Substitution of this analog inhibits in actively dividing cells.

Thymine bases are frequently oxidized to over time after the death of an organism.


Thymine imbalance causes mutation
During growth of bacteriophage T4, an imbalance of thymine availability, either a deficiency or an excess of thymine, causes increased .

The mutations caused by thymine deficiency appear to occur only at AT sites in DNA and are often AT to GC transition mutations.

In the bacterium , thymine deficiency was also found to cause the same mutation.


Theoretical aspects
In March 2015, NASA scientists reported that, for the first time, complex and of , including , and thymine, have been formed in the laboratory under conditions, using starting chemicals, such as , found in . Pyrimidine, like polycyclic aromatic hydrocarbons (PAHs), another carbon-rich compound, may have been formed in or in and gas clouds, according to the scientists. Thymine has not been found in meteorites, which suggests the first strands of DNA had to look elsewhere to obtain this building block. Thymine likely formed within some meteorite parent bodies, but may not have persisted within these bodies due to an reaction with hydrogen peroxide.


Synthesis

Laboratory synthesis
Thymine was first prepared by hydrolysis of the corresponding obtained from natural sources. Interest in its direct chemical synthesis began in the early 1900s: published a method starting from but a more practical synthesis used methylisothiourea in a condensation reaction with ethyl formyl propionate, followed by hydrolysis of the pyrimidine intermediate:
Many other preparative methods have been developed, including optimised conditions so that urea can be used directly in the reaction shown above, preferably with methyl formyl propionate.


See also


External links

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